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laevis oocytes</title> <meta name="description" content="Search results for: Xenopus laevis oocytes"> <meta name="keywords" content="Xenopus laevis oocytes"> <meta name="viewport" content="width=device-width, initial-scale=1, minimum-scale=1, maximum-scale=1, user-scalable=no"> <meta charset="utf-8"> <link href="https://cdn.waset.org/favicon.ico" type="image/x-icon" rel="shortcut icon"> <link href="https://cdn.waset.org/static/plugins/bootstrap-4.2.1/css/bootstrap.min.css" rel="stylesheet"> <link href="https://cdn.waset.org/static/plugins/fontawesome/css/all.min.css" rel="stylesheet"> <link href="https://cdn.waset.org/static/css/site.css?v=150220211555" rel="stylesheet"> </head> <body> <header> <div class="container"> <nav class="navbar navbar-expand-lg navbar-light"> <a class="navbar-brand" href="https://waset.org"> <img src="https://cdn.waset.org/static/images/wasetc.png" alt="Open Science Research Excellence" title="Open Science Research Excellence" /> </a> <button class="d-block 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action="https://publications.waset.org/abstracts/search"> <div id="custom-search-input"> <div class="input-group"> <i class="fas fa-search"></i> <input type="text" class="search-query" name="q" placeholder="Author, Title, Abstract, Keywords" value="Xenopus laevis oocytes"> <input type="submit" class="btn_search" value="Search"> </div> </div> </form> </div> </div> <div class="row mt-3"> <div class="col-sm-3"> <div class="card"> <div class="card-body"><strong>Commenced</strong> in January 2007</div> </div> </div> <div class="col-sm-3"> <div class="card"> <div class="card-body"><strong>Frequency:</strong> Monthly</div> </div> </div> <div class="col-sm-3"> <div class="card"> <div class="card-body"><strong>Edition:</strong> International</div> </div> </div> <div class="col-sm-3"> <div class="card"> <div class="card-body"><strong>Paper Count:</strong> 42</div> </div> </div> </div> <h1 class="mt-3 mb-3 text-center" style="font-size:1.6rem;">Search results for: Xenopus laevis oocytes</h1> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">42</span> The Response of 4-Hydroxybenzoic Acid on Kv1.4 Potassium Channel Subunit Expressed in Xenopus laevis Oocytes</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Fatin%20H.%20Mohamad">Fatin H. Mohamad</a>, <a href="https://publications.waset.org/abstracts/search?q=Jia%20H.%20Wong"> Jia H. Wong</a>, <a href="https://publications.waset.org/abstracts/search?q=Muhammad%20Bilal"> Muhammad Bilal</a>, <a href="https://publications.waset.org/abstracts/search?q=Abdul%20A.%20Mohamed%20Yusoff"> Abdul A. Mohamed Yusoff</a>, <a href="https://publications.waset.org/abstracts/search?q=Jafri%20M.%20Abdullah"> Jafri M. Abdullah</a>, <a href="https://publications.waset.org/abstracts/search?q=Jingli%20Zhang"> Jingli Zhang</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Kv1.4 is a Shaker-related member of voltage-gated potassium channel which can be associated with cardiac action potential but can also be found in Schaffer collateral and dentate gyrus. It has two inactivation mechanisms; the fast N-type and slow C-type. Kv1.4 produces rapid current inactivation. This A type potential of Kv1.4 makes it as a target in antiepileptic drugs (AEDs) selection. In this study, 4-hydroxybenzoic acid, which can be naturally found in bamboo shoots, were tested on its enhancement effect on potassium current of Kv1.4 channel expressed in Xenopus laevis oocytes using the two-microelectrode voltage clamp method. Current obtained were recorded and analyzed with pClamp software whereas statistical analysis were done by student t-test. The ratio of final / peak amplitude is an index of the activity of the Kv1.4 channel. The less the ratio, the greater the function of Kv1.4. The decrease of ratio of which by 1µM 4-hydroxybenzoic acid (n= 7), compared with 0.1% DMSO (vehicle), was mean= 47.62%, SE= 13.76%, P= 0.026 (statistically significant). It indicated more opening of Kv1.4 channels under 4-hydroxybenzoic acid. In conclusion, 4-hydroxybenzoic acid can enhance the function of Kv1.4 potassium channels, which is regarded as one of the mechanisms of antiepileptic treatment. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=antiepileptic" title="antiepileptic">antiepileptic</a>, <a href="https://publications.waset.org/abstracts/search?q=Kv1.4%20potassium%20channel" title=" Kv1.4 potassium channel"> Kv1.4 potassium channel</a>, <a href="https://publications.waset.org/abstracts/search?q=two-microelectrode%20voltage%20clamp" title=" two-microelectrode voltage clamp"> two-microelectrode voltage clamp</a>, <a href="https://publications.waset.org/abstracts/search?q=Xenopus%20laevis%20oocytes" title=" Xenopus laevis oocytes"> Xenopus laevis oocytes</a>, <a href="https://publications.waset.org/abstracts/search?q=4-hydroxybenzoic%20acid" title=" 4-hydroxybenzoic acid"> 4-hydroxybenzoic acid</a> </p> <a href="https://publications.waset.org/abstracts/38142/the-response-of-4-hydroxybenzoic-acid-on-kv14-potassium-channel-subunit-expressed-in-xenopus-laevis-oocytes" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/38142.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">362</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">41</span> Enhancement Effect of Compound 4-Hydroxybenzoic Acid from Petung Bamboo (Dendrocalamus Asper) Shoots on α1β2γ2S of GABA (A) Receptor Expressed in Xenopus laevis Oocytes- Preliminary Study on Its Anti-Epileptic Potential</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Muhammad%20Bilal">Muhammad Bilal</a>, <a href="https://publications.waset.org/abstracts/search?q=Amelia%20Jane%20Llyod"> Amelia Jane Llyod</a>, <a href="https://publications.waset.org/abstracts/search?q=Habsah%20Mohamad"> Habsah Mohamad</a>, <a href="https://publications.waset.org/abstracts/search?q=Jia%20Hui%20Wong"> Jia Hui Wong</a>, <a href="https://publications.waset.org/abstracts/search?q=Abdul%20Aziz%20Mohamed%20Yusoff"> Abdul Aziz Mohamed Yusoff</a>, <a href="https://publications.waset.org/abstracts/search?q=Jafri%20Malin%20Abdullah"> Jafri Malin Abdullah</a>, <a href="https://publications.waset.org/abstracts/search?q=Jingli%20Zhang"> Jingli Zhang</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Epilepsy is one of the major brain afflictions occurs with uncontrolled excitation of cortex; disturbed 50 million of world’s population. About 25 percent of patients subjected to adverse effects from antiepileptic drugs (AEDs) such as depression, nausea, tremors, gastrointestinal symptoms, osteoporosis, dizziness, weight change, drowsiness, fatigue are commonly observed indications; therefore, new drugs are required to cure epilepsy. GABA is principle inhibitory neurotransmitter, control excitation of the brain. Mutation or dysfunction of GABA receptor is one of the primary causes of epilepsy, which is confirmed from many acquired models of epilepsy like traumatic brain injury, kindling, and status epilepticus models of epilepsy. GABA receptor has 3 distinct types such as GABA (A), GABA (B), GABA(C).GABA (A) receptor has 20 different subunits, α1β2γ2 subunits composition of GABA (A) receptor is the most used combination of subunits for screening of compounds against epilepsy. We expressed α1β2γ2s subunits of GABA (A) Receptor in Xenopus leavis oocytes and examined the enhancement potential of 4-Hydroxybenzoic acid compound on GABA (A) receptor via two-electrode voltage clamp current recording technique. Bamboo shoots are the young, tender offspring of bamboo, which are usually harvested after a cultivating period of 2 weeks. Proteins, acids, fat, starch, carbohydrate, fatty acid, vitamin, dietary fiber, and minerals are the major constituent found systematically in bamboo shoots. These shoots reported to have anticancer, antiviral, antibacterial activity, also possess antioxidant properties due to the presence of phenolic compounds. Student t-test analysis suggested that 4- hydroxybenzoic acid positively allosteric GABA (A) receptor, increased normalized current amplitude to 1.0304±0.0464(p value 0.032) compared with vehicle. 4-Hydrobenzoic acid, a compound from Dendrocalamus Asper bamboo shoot gives new insights for future studies on bamboo shoots with motivation for extraction of more compounds to investigate their effects on human and rodents against epilepsy, insomnia, and anxiety. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=%CE%B11%CE%B22%CE%B32S" title="α1β2γ2S">α1β2γ2S</a>, <a href="https://publications.waset.org/abstracts/search?q=antiepileptic" title=" antiepileptic"> antiepileptic</a>, <a href="https://publications.waset.org/abstracts/search?q=bamboo%20shoots" title=" bamboo shoots"> bamboo shoots</a>, <a href="https://publications.waset.org/abstracts/search?q=epilepsy%20GABA%20%28A%29%20receptor" title=" epilepsy GABA (A) receptor"> epilepsy GABA (A) receptor</a>, <a href="https://publications.waset.org/abstracts/search?q=two-microelectrode%20voltage%20clamp" title=" two-microelectrode voltage clamp"> two-microelectrode voltage clamp</a>, <a href="https://publications.waset.org/abstracts/search?q=xenopus%20laevis%20oocytes" title=" xenopus laevis oocytes"> xenopus laevis oocytes</a> </p> <a href="https://publications.waset.org/abstracts/38143/enhancement-effect-of-compound-4-hydroxybenzoic-acid-from-petung-bamboo-dendrocalamus-asper-shoots-on-a1v2gh2s-of-gaba-a-receptor-expressed-in-xenopus-laevis-oocytes-preliminary-study-on-its-anti-epileptic-potential" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/38143.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">405</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">40</span> Capsaicin Derivatives Enhanced Activity of α1β2γ2S-Aminobutyric Acid Type a Receptor Expressed in Xenopus laevis Oocytes</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Jia%20H.%20Wong">Jia H. Wong</a>, <a href="https://publications.waset.org/abstracts/search?q=Jingli%20Zhang"> Jingli Zhang</a>, <a href="https://publications.waset.org/abstracts/search?q=Habsah%20Mohamad"> Habsah Mohamad</a>, <a href="https://publications.waset.org/abstracts/search?q=Iswatun%20H.%20Abdullah%20Ripain"> Iswatun H. Abdullah Ripain</a>, <a href="https://publications.waset.org/abstracts/search?q=Muhammad%20Bilal"> Muhammad Bilal</a>, <a href="https://publications.waset.org/abstracts/search?q=Amelia%20J.%20Lloyd"> Amelia J. Lloyd</a>, <a href="https://publications.waset.org/abstracts/search?q=Abdul%20A.%20Mohamed%20Yusoff"> Abdul A. Mohamed Yusoff</a>, <a href="https://publications.waset.org/abstracts/search?q=Jafri%20M.%20Abdullah"> Jafri M. Abdullah</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Epilepsy is one of the most common neurological diseases affecting more than 50 million of people worldwide. Epilepsy is a state of recurrent, spontaneous seizures with multiple syndromes and symptoms of different causes of brain dysfunction, prognosis, and treatments; characterized by transient, occasional and stereotyped interruptions of behavior whereby the excitatory-inhibitory activities within the central nervous system (CNS) are thrown out of balance due to various kinds of interferences. The goal of antiepileptic treatment is to enable patients to be free from seizures or to achieve control of seizures through surgical treatment and/or pharmacotherapy. Pharmacotherapy through AED plays an important role especially in countries with epilepsy treatment gap due to costs and availability of health facilities, skills and resources, yet there are about one-third of the people with epilepsy have drug-resistant seizures. Hence, this poses considerable challenges to the healthcare system and the effort in providing cost-effective treatment as well as the search for alternatives to treatment and management of epilepsy. Enhancement of γ-aminobutyric acid (GABA)-mediated inhibitory neurotransmission is one of the key mechanisms of actions of antiepileptic drugs. GABA type > a receptors (GABAAR) are ligand-gated ion channels that mediate rapid inhibitory neurotransmission upon the binding of GABA with a heteropentameric structure forming a central pore that is permeable to the influx of chloride ions in its activated state. The major isoform of GABAA receptors consists of two α1, two β2, and one γ2 subunit. It is the most abundantly expressed combinations in the brain and the most commonly researched through Xenopus laevis oocytes. With the advancing studies on ethnomedicine and traditional treatments using medicinal plants, increasing evidence reveal that spice and herb plants with medicinal properties play an important role in the treatment of ailments within communities across different cultures. Capsaicin is the primary natural capsaicinoid in hot peppers of plant genus Capsicum, consist of an aromatic ring, an amide linkage and a hydrophobic side chain. The study showed that capsaicins conferred neuroprotection in status epilepticus mouse models through anti-ictogenic, hypothermic, antioxidative, anti-inflammatory, and anti-apoptotic actions in a dose-dependent manner. In this study, five capsaicin derivatives were tested for their ability to increase the GABA-induced chloride current on α1β2γ2S of GABAAR expressed on Xenopus laevis oocytes using the method of two-microelectrode voltage clamp. Two of the capsaicin derivatives, IS5 (N-(4-hydroxy-3-methoxybenzyl)-3-methylbutyramide) and IS10 (N-(4-hydroxy-3-methoxybenzyl)-decanamide) at a concentration of 30µM were able to significantly increase the GABA-induced chloride current with p=0.002 and p=0.026 respectively. This study were able to show the enhancement effect of two capsaicin derivatives with moderate length of hydrocarbon chain on this receptor subtype, revealing the promising inhibitory activity of capsaicin derivatives through enhancement of GABA-induced chloride current and further investigations should be carried out to verify its antiepileptic effects in animal models. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=%CE%B11%CE%B22%CE%B32%20GABAA%20receptors" title="α1β2γ2 GABAA receptors">α1β2γ2 GABAA receptors</a>, <a href="https://publications.waset.org/abstracts/search?q=%CE%B11%CE%B22%CE%B32S" title=" α1β2γ2S"> α1β2γ2S</a>, <a href="https://publications.waset.org/abstracts/search?q=antiepileptic" title=" antiepileptic"> antiepileptic</a>, <a href="https://publications.waset.org/abstracts/search?q=capsaicin%20derivatives" title=" capsaicin derivatives"> capsaicin derivatives</a>, <a href="https://publications.waset.org/abstracts/search?q=two-microelectrode%20voltage%20clamp" title=" two-microelectrode voltage clamp"> two-microelectrode voltage clamp</a>, <a href="https://publications.waset.org/abstracts/search?q=Xenopus%20laevis%20oocytes" title=" Xenopus laevis oocytes"> Xenopus laevis oocytes</a> </p> <a href="https://publications.waset.org/abstracts/38140/capsaicin-derivatives-enhanced-activity-of-a1v2gh2s-aminobutyric-acid-type-a-receptor-expressed-in-xenopus-laevis-oocytes" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/38140.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">362</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">39</span> The Effect of Ethylene Glycol on Cryopreserved Bovine Oocytes</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Sri%20Wahjuningsih">Sri Wahjuningsih</a>, <a href="https://publications.waset.org/abstracts/search?q=Nur%20Ihsan"> Nur Ihsan</a>, <a href="https://publications.waset.org/abstracts/search?q=Hadiah"> Hadiah</a> </p> <p class="card-text"><strong>Abstract:</strong></p> In the embryo transfer program, to address the limited production of embryos in vivo, in vitro embryo production has become an alternative approach that is relatively inexpensive. One potential source of embryos that can be developed is to use immature oocytes then conducted in vitro maturation and in vitro fertilization. However, obstacles encountered were oocyte viability mammals have very limited that it cannot be stored for a long time, so we need oocyte cryopreservation. The research was conducted to know the optimal concentration use of ethylene glycol as a cryoprotectant on oocytes freezing.Material use in this research was immature oocytes; taken from abbatoir which was aspirated from follicle with diameter 2-6 mm. Concentration ethylen glycol used were 0,5 M, I M, 1,5 M and 2M. The freezing method used was conventional method combined with a five-step protocol washing oocytes from cryoprotectant after thawing. The result showed that concentration ethylen glycol have the significant effect (P<0.05) on oocytes quality after thawing and in vitro maturation. It was concluded that concentration 1,5 M was the best concentration for freezing oocytes using conventional method. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=bovine" title="bovine">bovine</a>, <a href="https://publications.waset.org/abstracts/search?q=conventional%20freezing" title=" conventional freezing"> conventional freezing</a>, <a href="https://publications.waset.org/abstracts/search?q=ethylen%20glycol" title=" ethylen glycol"> ethylen glycol</a>, <a href="https://publications.waset.org/abstracts/search?q=oocytes" title=" oocytes"> oocytes</a> </p> <a href="https://publications.waset.org/abstracts/39761/the-effect-of-ethylene-glycol-on-cryopreserved-bovine-oocytes" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/39761.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">364</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">38</span> Effect of Follicular Fluid on in vitro Maturation and Gene Expression in Ovine Oocytes</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Al-Mutary%20M.">Al-Mutary M.</a>, <a href="https://publications.waset.org/abstracts/search?q=Alhimaidi%20A."> Alhimaidi A.</a>, <a href="https://publications.waset.org/abstracts/search?q=Al-Ghadi%20M.%20%20Iwamoto%20D.">Al-Ghadi M. Iwamoto D.</a>, <a href="https://publications.waset.org/abstracts/search?q=Javed%20Ahmad.%20Abdulaziz%20A.%20Al-Khedhairy"> Javed Ahmad. Abdulaziz A. Al-Khedhairy</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The aim of the present study was to evaluate the effect of ovine follicular fluid supplementation during IVM of sheep oocytes on the resumption of meiosis, glutathione (GSH) content and expression of Bax, Bcl-2, and HSPB1 genes. Sheep ovaries were collected from Riyadh slaughterhouse, KSA. Oocytes were aspirated from 3-6 mm follicles. Ovine oocytes were cultured in maturation medium with 0% (control), 10%, 20%, 40% of ovine follicular fluid for 24 h. Results indicated that the rate of oocyte maturation was significantly (P≤0.05) decreased in 40% OFF (36.87%) versus the control (61.3%), 10% OFF (63.95%) and 20% OFF (64.08%). Supplementation of 10% OFF to IVM medium induced an intra-oocyte GSH concentration significantly higher than that found in ovine oocytes cultured with 20% OFF and 40% OFF and similar to the GSH content in oocytes cultured without FF. Real time polymerase chain reaction analysis for gene expression revealed no differences in Bax, Bcl-2, HSPB1 genes between control and 10% OFF group, whereas they were strongly expressed in 20% OFF and 40% OFF (P < 0.05) when compared to the control and 10% OFF. In conclusion the addition of 10% OFF to the IVM culture of sheep oocytes is recommended to support cytoplasmic maturation and increase oocytes competence. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=IVM" title="IVM">IVM</a>, <a href="https://publications.waset.org/abstracts/search?q=oocyte%20maturation" title=" oocyte maturation"> oocyte maturation</a>, <a href="https://publications.waset.org/abstracts/search?q=gene%20expression" title=" gene expression"> gene expression</a>, <a href="https://publications.waset.org/abstracts/search?q=follicular%20fluid" title=" follicular fluid"> follicular fluid</a> </p> <a href="https://publications.waset.org/abstracts/16818/effect-of-follicular-fluid-on-in-vitro-maturation-and-gene-expression-in-ovine-oocytes" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/16818.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">362</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">37</span> Effects of Fenugreek Seed Extract on in vitro Maturation and Subsequent Development of Sheep Oocytes</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Ibrahim%20A.%20H.%20Barakat">Ibrahim A. H. Barakat</a>, <a href="https://publications.waset.org/abstracts/search?q=Ahmed%20R.%20Al-Himaidi"> Ahmed R. Al-Himaidi</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The present study was conducted to determine the role and optimum concentration of fenugreek seed extract during in-vitro maturation on in-vitro maturation and developmental competence of Neaimi sheep oocytes following in-vitro fertilization. The Cumulus Oocyte Complexes (COCs) collected from sheep slaughterhouse ovaries were randomly divided into three groups, and they were matured for 24 hrs. in maturation medium containing fenugreek seed extract (0, 1 and 10 µg ml-1). Oocytes of a control group were matured in a medium containing 1 µg ml-1 estradiol 17β. After maturation, half of oocytes were fixed and stained for evaluation of nuclear maturation. The rest of oocytes were fertilized in vitro with fresh semen, then cultured for 9 days for the assessment of the developmental capacity of the oocytes. The results showed that the mean values of oocytes with expanded cumulus cells percentage were not significantly different among all groups (P < 0.05). But nuclear maturation rate of oocytes matured with 10 µg ml-1 fenugreek seed extract was significantly higher than that of the control group. The maturation rate and development to morula and blastocyst stage for oocytes matured at 10 µg ml-1 fenugreek seed extract was significantly higher than those matured at 1µg ml-1 of fenugreek seed extract and the control group. In conclusion, better maturation and developmental capacity rate to morula and blastocyst stage were obtained by the addition of 10 µg ml-1 fenugreek seed extract to maturation medium than addition of 1 µg ml-1 estradiol-17β (P < 0.05). <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=fenugreek%20seed%20extract" title="fenugreek seed extract">fenugreek seed extract</a>, <a href="https://publications.waset.org/abstracts/search?q=in%20vitro%20maturation" title=" in vitro maturation"> in vitro maturation</a>, <a href="https://publications.waset.org/abstracts/search?q=sheep%20oocytes" title=" sheep oocytes"> sheep oocytes</a>, <a href="https://publications.waset.org/abstracts/search?q=in%20vitro%20fertilization" title=" in vitro fertilization"> in vitro fertilization</a>, <a href="https://publications.waset.org/abstracts/search?q=embryo%20development" title=" embryo development"> embryo development</a> </p> <a href="https://publications.waset.org/abstracts/3185/effects-of-fenugreek-seed-extract-on-in-vitro-maturation-and-subsequent-development-of-sheep-oocytes" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/3185.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">392</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">36</span> Sensitivity of Steindachneridion parahybae Mature Oocytes versus Embryos at Low Temperature</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Tais%20Silva%20Lopes">Tais Silva Lopes</a>, <a href="https://publications.waset.org/abstracts/search?q=Danilo%20Caneppele"> Danilo Caneppele</a>, <a href="https://publications.waset.org/abstracts/search?q=Elizabeth%20Romagosa"> Elizabeth Romagosa</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Surubim-do-Paraíba, Steindachneridion parahybae is a species of South American fish in critical conditions of extinction. Researches have been developed with the objective of conserving the biological material of this species. We evaluated the cooling of mature oocytes in the cryoprotective solutions containing the following alcohols: methanol, Propylene glycol and DMSO, each at concentrations of 1M, 2M and 4M, totaling nine treatments. After being submitted to treatments, the oocytes were maintained for 120 minutes in cooling to -5.52±2.58⁰C. A sample of oocytes was submitted to negative control (NC), kept in 90% L-15 solution, and positive control (PC), fertilized and taken directly to the incubator. Fertilization and hatching rates were evaluated. In order to compare the sensitivity of oocytes to embryos of the same species, the embryos maintained as CP in the previous assay were used in the free-flow stage (about 22 hours post fertilization) and submitted to the same treatments (prepared in distilled water) and also cooled for 120 min. The evaluation was done by the hatch rate. There was no fertilization rate of the oocytes submitted to the cooling with propylene glycol; the other cryoprotectants presented values of at most 3.7% of fertilization (Methanol 1M), and no treatment completed development until hatching. The cooled embryos had a significant percentage of normal larvae in all treatments, but inversely proportional to the increase in the concentration of the alcohols. DMSO 1M was the most promising treatment for embryo cooling, with 41.7% ± 20.2 of normal larvae, while mature oocytes were highly sensitive to cold. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=cryoconservation" title="cryoconservation">cryoconservation</a>, <a href="https://publications.waset.org/abstracts/search?q=cooling" title=" cooling"> cooling</a>, <a href="https://publications.waset.org/abstracts/search?q=embryos" title=" embryos"> embryos</a>, <a href="https://publications.waset.org/abstracts/search?q=freezing" title=" freezing"> freezing</a>, <a href="https://publications.waset.org/abstracts/search?q=oocytes" title=" oocytes"> oocytes</a>, <a href="https://publications.waset.org/abstracts/search?q=south%20American%20fish" title=" south American fish"> south American fish</a> </p> <a href="https://publications.waset.org/abstracts/72601/sensitivity-of-steindachneridion-parahybae-mature-oocytes-versus-embryos-at-low-temperature" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/72601.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">241</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">35</span> Perfluoroheptanoic Acid Affects Xenopus Embryo Embryogenesis by Inducing the Phosphorylation of ERK and JNK</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Chowon%20Kim">Chowon Kim</a>, <a href="https://publications.waset.org/abstracts/search?q=Yoo-Kyung%20Kim"> Yoo-Kyung Kim</a>, <a href="https://publications.waset.org/abstracts/search?q=Kyeong%20Yeon%20Park"> Kyeong Yeon Park</a>, <a href="https://publications.waset.org/abstracts/search?q=Hyun-Shik%20Lee"> Hyun-Shik Lee</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Perfluoroalkyl compounds (PFCs) are globally distributed synthetic compounds that are known to adversely affect human health. Developmental toxicity assessment of PFCs is important to facilitate the evaluation of their environmental impact. In the present study, we assessed the developmental toxicity and teratogenicity of PFCs with different numbers of carbon atoms on Xenopus embryogenesis. An initial frog embryo teratogenicity assay-Xenopus (FETAX) assay was performed that identified perfluorohexanoic (PFHxA) and perfluoroheptanoic (PFHpA) acids as potential teratogens and developmental toxicants. The mechanism underlying this teratogenicity was also investigated by measuring the expression of tissue-specific biomarkers such as phosphotyrosine‑binding protein, xPTB (liver); NKX2.5 (heart); and Cyl18 (intestine). Whole‑mount in situ hybridization, reverse transcriptase‑polymerase chain reaction (RT-PCR), and histologic analyses detected severe defects in the liver and heart following exposure to PFHxA or PFHpA. In addition, immunoblotting revealed that PFHpA significantly increased the phosphorylation of extracellular signal-regulated kinase (ERK) and c-Jun N-terminal kinase (JNK), while PFHxA slightly increased these, as compared with the control. These results suggest that PFHxA and PFHpA are developmental toxicants and teratogens, with PFHpA producing more severe effects on liver and heart development through the induction of ERK and JNK phosphorylation. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=PFCs" title="PFCs">PFCs</a>, <a href="https://publications.waset.org/abstracts/search?q=ERK" title=" ERK"> ERK</a>, <a href="https://publications.waset.org/abstracts/search?q=JNK" title=" JNK"> JNK</a>, <a href="https://publications.waset.org/abstracts/search?q=xenopus" title=" xenopus"> xenopus</a> </p> <a href="https://publications.waset.org/abstracts/46964/perfluoroheptanoic-acid-affects-xenopus-embryo-embryogenesis-by-inducing-the-phosphorylation-of-erk-and-jnk" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/46964.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">296</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">34</span> Follicular Fluid Proteins and Cells Study on Small, Medium, and Large Follicles of Large White Pig</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Mayuva%20Youngsabanant-Areekijseree">Mayuva Youngsabanant-Areekijseree</a>, <a href="https://publications.waset.org/abstracts/search?q=Chanikarn%20Srinark"> Chanikarn Srinark</a>, <a href="https://publications.waset.org/abstracts/search?q=S.%20Sengsai"> S. Sengsai</a>, <a href="https://publications.waset.org/abstracts/search?q=Mayuree%20Pumipaiboon"> Mayuree Pumipaiboon</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Our project was aimed at morphology of oocytes, follicle cells and follicular fluid proteins study of Large White pig (at local slaughter house in Nakhon Pathom Province). The porcine oocytes and follicular fluid of healthy small follicles (1-2 mm), medium follicles (3-6 mm in diameters) and large follicles (7-8 mm and 10 mm in diameter) were aspirated and collected from the ovary by sterile technique. Then, the oocytes and the follicle cells were separated from the fluid. The oocytes were round shape and surrounded by zona pellucida with numerous layers of cumulus cells. Based on the number of cumulus cell layers surrounding oocytes, the oocytes were classified into 5 types, which were intact-, multi-, partial-cumulus layer oocyte, completely denuded oocyte and degenerative oocyte. The collected oocytes showed high percentages of intact- and multi- cumulus cell layers in the small follicles (53.48%) medium follicles (56.94%) and large follicles (56.52%) which have high potential to develop into mature oocytes in vitro. Proteins from follicular fluid of 3 size follicles were separated by SDS-PAGE and LC/MS/MS. The molecular weight of follicular fluid proteins from the small follicles were 24, 60-65, 79, 110, 140, 160, and > 220 kDa. Meanwhile, the follicular fluid protein from medium and large follicle contained 52, 65, 79, 90, 110, 120, 160, 190 and > 220 kDa. Almost all proteins played important roles in promoting and regulating growth and development of oocytes and ovulation. This finding was an initial tool for in vitro testing and applied biotechnology research. Acknowledgements: The project was funded by a grant from Silpakorn University Research & Development Institute (SURDI) and Faculty of Science, Silpakorn University, Thailand. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=follicular%20fluid%20protein" title="follicular fluid protein">follicular fluid protein</a>, <a href="https://publications.waset.org/abstracts/search?q=LC%2FMS%2FMS" title=" LC/MS/MS"> LC/MS/MS</a>, <a href="https://publications.waset.org/abstracts/search?q=porcine%20oocyte" title=" porcine oocyte"> porcine oocyte</a>, <a href="https://publications.waset.org/abstracts/search?q=SDS-PAGE" title=" SDS-PAGE"> SDS-PAGE</a>, <a href="https://publications.waset.org/abstracts/search?q=reproductive%20biology" title=" reproductive biology"> reproductive biology</a> </p> <a href="https://publications.waset.org/abstracts/59264/follicular-fluid-proteins-and-cells-study-on-small-medium-and-large-follicles-of-large-white-pig" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/59264.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">235</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">33</span> Effect of IGF-I on Ovine Oocytes Maturation and Subsequent Embryo Development following in Vitro Fertilization (IVF)</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Babak%20Qasemi-Panahi">Babak Qasemi-Panahi</a>, <a href="https://publications.waset.org/abstracts/search?q=Gholamali%20Moghaddam"> Gholamali Moghaddam</a>, <a href="https://publications.waset.org/abstracts/search?q=Seyed-Abbas%20Rafat"> Seyed-Abbas Rafat</a>, <a href="https://publications.waset.org/abstracts/search?q=Hossein%20Daghigh%20Kia"> Hossein Daghigh Kia</a>, <a href="https://publications.waset.org/abstracts/search?q=Mansoureh%20Movahedin"> Mansoureh Movahedin</a>, <a href="https://publications.waset.org/abstracts/search?q=Reza%20Hadavi"> Reza Hadavi</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The objective of this study was to determine the effects of IGF-I on ovine oocytes maturation and subsequent development of embryos derived from in vitro fertilization (IVF). In vitro maturation (IVM) of oocytes and in vitro culture (IVC) of embryos was conducted with or without 100 ng/mL IGF-1. In the IGF-I treated group, mean percentage of oocyte maturation was significantly higher than the control group (57.67 ± 3.04 versus 49.81 ± 3.04%, respectively, P < 0.05). However, in comparison with control group, there was no significant effect of IGF-1 on rates of cleavage, morula, and blastocyst formation (85% versus 84%; 63% versus 65%, and 40% to 39%, respectively). These data demonstrate that IGF-I has a positive effect on ovine oocyte maturation rate, but it has not the significant outcome on embryo development. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=ovine" title="ovine">ovine</a>, <a href="https://publications.waset.org/abstracts/search?q=IGF-I" title=" IGF-I"> IGF-I</a>, <a href="https://publications.waset.org/abstracts/search?q=IVM" title=" IVM"> IVM</a>, <a href="https://publications.waset.org/abstracts/search?q=ICSI" title=" ICSI"> ICSI</a> </p> <a href="https://publications.waset.org/abstracts/21011/effect-of-igf-i-on-ovine-oocytes-maturation-and-subsequent-embryo-development-following-in-vitro-fertilization-ivf" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/21011.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">688</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">32</span> Effect of Vitrification on Embryos Euploidy Obtained from Thawed Oocytes</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Natalia%20Buderatskaya">Natalia Buderatskaya</a>, <a href="https://publications.waset.org/abstracts/search?q=Igor%20Ilyin"> Igor Ilyin</a>, <a href="https://publications.waset.org/abstracts/search?q=Julia%20Gontar"> Julia Gontar</a>, <a href="https://publications.waset.org/abstracts/search?q=Sergey%20Lavrynenko"> Sergey Lavrynenko</a>, <a href="https://publications.waset.org/abstracts/search?q=Olga%20Parnitskaya"> Olga Parnitskaya</a>, <a href="https://publications.waset.org/abstracts/search?q=Ekaterina%20Ilyina"> Ekaterina Ilyina</a>, <a href="https://publications.waset.org/abstracts/search?q=Eduard%20Kapustin"> Eduard Kapustin</a>, <a href="https://publications.waset.org/abstracts/search?q=Yana%20Lakhno"> Yana Lakhno</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Introduction: It is known that cryopreservation of oocytes has peculiar features due to the complex structure of the oocyte. One of the most important features is that mature oocytes contain meiotic division spindle which is very sensitive even to the slightest variation in temperature. Thus, the main objective of this study is to analyse the resulting euploid embryos obtained from thawed oocytes in comparison with the data of preimplantation genetic screening (PGS) in fresh embryo cycles. Material and Methods: The study was conducted at 'Medical Centre IGR' from January to July 2016. Data were analysed for 908 donor oocytes obtained in 67 cycles of assisted reproductive technologies (ART), of which 693 oocytes were used in the 51 'fresh' cycles (group A), and 215 oocytes - 16 ART programs with vitrification female gametes (group B). The average age of donors in the groups match 27.3±2.9 and 27.8±6.6 years. Stimulation of superovulation was conducted the standard way. Vitrification was performed in 1-2 hours after transvaginal puncture and thawing of oocytes were carried out in accordance with the standard protocol of Cryotech (Japan). Manipulation ICSI was performed 4-5 hours after transvaginal follicle puncture for fresh oocytes, or after defrosting - for vitrified female gametes. For the PGS, an embryonic biopsy was done on the third or on the fifth day after fertilization. Diagnostic procedures were performed using fluorescence in situ hybridization with the study of such chromosomes as 13, 16, 18, 21, 22, X, Y. Only morphologically quality blastocysts were used for the transfer, the estimation of which corresponded to the Gardner criteria. The statistical hypotheses were done using the criteria t, x^2 at a significance levels p<0.05, p<0.01, p<0.001. Results: The mean number of mature oocytes per cycle in group A was 13.58±6.65 and in group B - 13.44±6.68 oocytes for patient. The survival of oocytes after thawing totaled 95.3% (n=205), which indicates a highly effective quality of performed vitrification. The proportion of zygotes in the group A corresponded to 91.1%(n=631), in the group B – 80.5%(n=165), which shows statistically significant difference between the groups (p<0.001) and explained by non-viable oocytes elimination after vitrification. This is confirmed by the fact that on the fifth day of embryos development a statistically significant difference in the number of blastocysts was absent (p>0.05), and constituted respectively 61.6%(n=389) and 63.0%(n=104) in the groups. For the PGS performing 250 embryos analyzed in the group A and 72 embryos - in the group B. The results showed that euploidy in the studied chromosomes were 40.0%(n=100) embryos in the group A and 41.7% (n=30) - in the group B, which shows no statistical significant difference (p>0.05). The indicators of clinical pregnancies in the groups amounted to 64.7% (22 pregnancies per 34 embryo transfers) and 61.5% (8 pregnancies per 13 embryo transfers) respectively, and also had no significant difference between the groups (p>0.05). Conclusions: The results showed that the vitrification does not affect the resulting euploid embryos in assisted reproductive technologies and are not reflected in their morphological characteristics in ART programs. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=euploid%20embryos" title="euploid embryos">euploid embryos</a>, <a href="https://publications.waset.org/abstracts/search?q=preimplantation%20genetic%20screening" title=" preimplantation genetic screening"> preimplantation genetic screening</a>, <a href="https://publications.waset.org/abstracts/search?q=thawing%20oocytes" title=" thawing oocytes"> thawing oocytes</a>, <a href="https://publications.waset.org/abstracts/search?q=vitrification" title=" vitrification"> vitrification</a> </p> <a href="https://publications.waset.org/abstracts/57504/effect-of-vitrification-on-embryos-euploidy-obtained-from-thawed-oocytes" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/57504.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">334</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">31</span> The Localization and Function of p38α Mitogen-Activated Protein Kinase (MAPK) in Rat Oocytes</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Shifu%20Hu">Shifu Hu</a>, <a href="https://publications.waset.org/abstracts/search?q=Qiong%20Yu"> Qiong Yu</a>, <a href="https://publications.waset.org/abstracts/search?q=Wei%20Xia"> Wei Xia</a>, <a href="https://publications.waset.org/abstracts/search?q=Changhong%20Zhu"> Changhong Zhu</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Background: P38α MAPK, which is a member of the canonical MAPK family, is activated in response to various extracellular stresses and plays a role in multiple cellular processes. It is well known that p38α MAPK play vital roles in oocyte maturation, but the localization and functional roles of p38α MAPK during the meiotic maturation of rat oocytes remain unknown. Study Design: In this study, western-blot and immunofluorescent staining were used to investigate the expression and subcellular localization of p38α MAPK during the meiotic maturation of rat oocytes. SB203580, a specific inhibitor of p38α MAPK, was used to study the roles of p38α MAPK in the meiotic cell cycle of rat oocytes. Results: The results found that p38α MAPK phosphorylation (p-p38α MAPK, indicative of p38α MAPK activation) was low at the germinal vesicle (GV) stage, increased 3 h after germinal vesicle breakdown (GVBD), and maintained its maximum at MI (metaphase I) or M II (metaphase II). The p-p38α MAPK mainly accumulated in the germinal vesicle and had no obvious expression in the nucleus. From GVBD to M II, p-p38α MAPK was distributed in the cytoplasm around either the chromosomes or the spindle. We used SB203580, an inhibitor of p38α MAPK, to investigate the possible functional role of p38α MAPK during rat oocyte meiotic maturation. Treatment of GV stage oocytes with 20 μM SB203580 blocked p-p38α MAPK activity, and the spindles appeared abnormal. Additionally, the rate of GVBD after 3h of culture with 20 μM SB203580 (58.8%) was significantly inhibited compared with the control (82.5%, p < 0.05), and the polar body extrusion rate after 12 h of culture with SB203580 was also significantly decreased compared with the control (40.1 vs. 73.3%, p < 0.05). Conclusions: These data indicate that p38α MAPK may play a vital role in rat oocyte meiotic maturation. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=meiotic%20maturation" title="meiotic maturation">meiotic maturation</a>, <a href="https://publications.waset.org/abstracts/search?q=oocyte" title=" oocyte"> oocyte</a>, <a href="https://publications.waset.org/abstracts/search?q=p38%CE%B1%20MAPK" title=" p38α MAPK"> p38α MAPK</a>, <a href="https://publications.waset.org/abstracts/search?q=spindle" title=" spindle"> spindle</a> </p> <a href="https://publications.waset.org/abstracts/87813/the-localization-and-function-of-p38a-mitogen-activated-protein-kinase-mapk-in-rat-oocytes" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/87813.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">159</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">30</span> Effect of Depth on the Distribution of Zooplankton in Wushishi Lake Minna, Niger State, Nigeria</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Adamu%20Zubairu%20Mohammed">Adamu Zubairu Mohammed</a>, <a href="https://publications.waset.org/abstracts/search?q=Fransis%20Oforum%20Arimoro"> Fransis Oforum Arimoro</a>, <a href="https://publications.waset.org/abstracts/search?q=Salihu%20Maikudi%20Ibrahim"> Salihu Maikudi Ibrahim</a>, <a href="https://publications.waset.org/abstracts/search?q=Y.%20I.%20Auta"> Y. I. Auta</a>, <a href="https://publications.waset.org/abstracts/search?q=T.%20I.%20Arowosegbe"> T. I. Arowosegbe</a>, <a href="https://publications.waset.org/abstracts/search?q=Y.%20Abdullahi"> Y. Abdullahi</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The present study was conducted to evaluate the effect of depth on the distribution of zooplankton and some physicochemical parameters in Tungan Kawo Lake (Wushishi dam). Water and zooplankton samples were collected from the surface, 3.0 meters deep and 6.0 meters deep, for a period of 24 hours for six months. Standard procedures were adopted for the determination of physicochemical parameters. Results have shown significant differences in the pH, DO, BOD Hardness, Na, and Mg. A total of 1764 zooplankton were recorded, comprising 35 species, with cladocera having 18 species (58%), 14 species of copepoda (41%), 3 species of diptera (1.0%). Results show that more of the zooplankton were recorded in the 3.0 meters-deep region compared to the two other depts and a significant difference was observed in the distribution of Ceriodaphnia dubia, Daphnia laevis, and Leptodiaptomus coloradensis. Though the most abundant zooplankton was recorded in the 3.0 meters deep, Leptodiaptomus coloradesnsis, which was observed in the 6.0 meters deep as the most individual observed, this was followed by Daphnia laevis. Canonical correspondence analysis between physicochemical parameters and the zooplankton indicated a good relationship in the Lake. Ceriodaphnia dubia was found to have a good association with oxygen, sodium, and potassium, while Daphnia laevis and Leptodiaptomus coloradensis are in good relationship with magnesium and phosphorus. It was generally observed that this depth does not have much influence on the distribution of zooplankton in Wushishi Lake. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=zooplankton" title="zooplankton">zooplankton</a>, <a href="https://publications.waset.org/abstracts/search?q=standard%20procedures" title=" standard procedures"> standard procedures</a>, <a href="https://publications.waset.org/abstracts/search?q=canonical%20correspondence%20analysis" title=" canonical correspondence analysis"> canonical correspondence analysis</a>, <a href="https://publications.waset.org/abstracts/search?q=Wushishi" title=" Wushishi"> Wushishi</a>, <a href="https://publications.waset.org/abstracts/search?q=canonical" title=" canonical"> canonical</a>, <a href="https://publications.waset.org/abstracts/search?q=physicochemical%20parameter" title=" physicochemical parameter"> physicochemical parameter</a> </p> <a href="https://publications.waset.org/abstracts/172173/effect-of-depth-on-the-distribution-of-zooplankton-in-wushishi-lake-minna-niger-state-nigeria" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/172173.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">90</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">29</span> Understanding Chromosome Movement in Starfish Oocytes</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Bryony%20Davies">Bryony Davies</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Many cell and tissue culture practices ignore the effects of gravity on cell biology, and little is known about how cell components may move in response to gravitational forces. Starfish oocytes provide an excellent model for interrogating the movement of cell components due to their unusually large size, ease of handling, and high transparency. Chromosomes from starfish oocytes can be visualised by microinjection of the histone-H2B-mCherry plasmid into the oocytes. The movement of the chromosomes can then be tracked by live-cell fluorescence microscopy. The results from experiments using these methods suggest that there is a replicable downward movement of centrally located chromosomes at a median velocity of 0.39 μm/min. Chromosomes nearer the nuclear boundary showed more restricted movement. Chromosome density and shape could also be altered by microinjection of restriction enzymes, primarily Alu1, before imaging. This was found to alter the speed of chromosome movement, with chromosomes from Alu1-injected nuclei showing a median downward velocity of 0.60 μm/min. Overall, these results suggest that there is a non-negligible movement of chromosomes in response to gravitational forces and that this movement can be altered by enzyme activity. Future directions based on these results could interrogate if this observed downward movement extends to other cell components and to other cell types. Additionally, it may be important to understand whether gravitational orientation and vertical positioning of cell components alter cell behaviour. The findings here may have implications for current cell culture practices, which do not replicate cell orientations or external forces experienced in vivo. It is possible that a failure to account for gravitational forces in 2D cell culture alters experimental results and the accuracy of conclusions drawn from them. Understanding possible behavioural changes in cells due to the effects of gravity would therefore be beneficial. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=starfish" title="starfish">starfish</a>, <a href="https://publications.waset.org/abstracts/search?q=oocytes" title=" oocytes"> oocytes</a>, <a href="https://publications.waset.org/abstracts/search?q=live-cell%20imaging" title=" live-cell imaging"> live-cell imaging</a>, <a href="https://publications.waset.org/abstracts/search?q=microinjection" title=" microinjection"> microinjection</a>, <a href="https://publications.waset.org/abstracts/search?q=chromosome%20dynamics" title=" chromosome dynamics"> chromosome dynamics</a> </p> <a href="https://publications.waset.org/abstracts/158323/understanding-chromosome-movement-in-starfish-oocytes" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/158323.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">104</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">28</span> Cumulus-Oocyte Complexes and Follicular Fluid Proteins of Pig during Folliculogenesis</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Panomporn%20Wisuthseriwong">Panomporn Wisuthseriwong</a>, <a href="https://publications.waset.org/abstracts/search?q=Hatairuk%20Tungkasen"> Hatairuk Tungkasen</a>, <a href="https://publications.waset.org/abstracts/search?q=Siyaporn%20Namsongsan"> Siyaporn Namsongsan</a>, <a href="https://publications.waset.org/abstracts/search?q=Chanikarn%20Srinark"> Chanikarn Srinark</a>, <a href="https://publications.waset.org/abstracts/search?q=Mayuva%20Youngsabanant-Areekijseree"> Mayuva Youngsabanant-Areekijseree</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The objective of the present study was to evaluate the morphology of porcine cumulus-oocyte complexes (pCOCs) and follicular fluid during follicular development. The samples were obtained from local slaughterhouses in Nakorn Pathom Province, Thailand. Pigs were classified as either in the follicular phase or luteal phase. Porcine follicles (n = 3,510) were categorized as small (1-3 mm in diameters; n=2,910), medium (4-6 mm in diameters; n=530) and large (7-8 mm in diameters; n=70). Then pCOCs and follicular fluid were collected. Finally, we found that the oocytes can be categorized into intact cumulus cells layer oocyte, multi-cumulus cells layer oocyte, partial cumulus cells layer oocyte, completely denuded oocyte and degenerated oocyte. They showed high percentage of intact and multi-cumulus cells layer oocytes from small follicles (54.68%) medium follicles (69.06%) and large follicles (68.57%), which have high potential to develop into matured oocytes in vitro. Protein composition of the follicular fluid was separated by SDS-PAGE technique. The result shows that the protein molecular weight in the small and medium follicles are 23, 50, 66, 75, 92, 100, 132, 163, 225 and >225 kDa. Meanwhile, protein molecular weight in large follicles are 12, 16, 23, 50, 66, 75, 92, 100, 132, 163, 225 and >225 kDa. All proteins play an important role in promotion and regulation on development, maturation of oocytes and regulation of ovulation. We conclude that the results of discovery can be used porcine secretion proteins for supplement in IVM/IVF technology. Acknowledgements: The project was funded by a grant from Silpakorn University Research and Development Institute (SURDI) and Faculty of Science, Silpakorn University, Thailand. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=porcine%20follicles" title="porcine follicles">porcine follicles</a>, <a href="https://publications.waset.org/abstracts/search?q=porcine%20oocyte" title=" porcine oocyte"> porcine oocyte</a>, <a href="https://publications.waset.org/abstracts/search?q=follicular%20fluid" title=" follicular fluid"> follicular fluid</a>, <a href="https://publications.waset.org/abstracts/search?q=SDS-PAGE" title=" SDS-PAGE"> SDS-PAGE</a> </p> <a href="https://publications.waset.org/abstracts/57600/cumulus-oocyte-complexes-and-follicular-fluid-proteins-of-pig-during-folliculogenesis" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/57600.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">258</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">27</span> Analysis of the Blastocysts Chromosomal Set Obtained after the Use of Donor Oocyte Cytoplasmic Transfer Technology</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Julia%20Gontar">Julia Gontar</a>, <a href="https://publications.waset.org/abstracts/search?q=Natalia%20Buderatskaya"> Natalia Buderatskaya</a>, <a href="https://publications.waset.org/abstracts/search?q=Igor%20Ilyin"> Igor Ilyin</a>, <a href="https://publications.waset.org/abstracts/search?q=Olga%20Parnitskaya"> Olga Parnitskaya</a>, <a href="https://publications.waset.org/abstracts/search?q=Sergey%20Lavrynenko"> Sergey Lavrynenko</a>, <a href="https://publications.waset.org/abstracts/search?q=Eduard%20Kapustin"> Eduard Kapustin</a>, <a href="https://publications.waset.org/abstracts/search?q=Ekaterina%20Ilyina"> Ekaterina Ilyina</a>, <a href="https://publications.waset.org/abstracts/search?q=Yana%20Lakhno"> Yana Lakhno</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Introduction: It is well known that oocytes obtained from older reproductive women have accumulated mitochondrial DNA mutations, which negatively affects the morphology of a developing embryo and may lead to the birth of a child with mitochondrial disease. Special techniques have been developed to allow a donor oocyte cytoplasmic transfer with the parents’ biological nuclear DNA retention. At the same time, it is important to understand whether the procedure affects the future embryonic chromosome sets as the nuclear DNA is the transfer subject in this new complex procedure. Material and Methods: From July 2015 to July 2016, the investigation was carried out in the Medical Centre IGR. 34 donor oocytes (group A) were used for the manipulation with the aim of donating cytoplasm: 21 oocytes were used for zygotes pronuclear transfer and oocytes 13 – for the spindle transfer. The mean age of the oocyte donors was 28.4±2.9 years. The procedure was performed using Nikon Ti Eclipse inverted microscope equipped with the micromanipulators Narishige system (Japan), Saturn 3 laser console (UK), Oosight imaging systems (USA). For the preimplantation genetic screening (PGS) blastocyst biopsy was performed, trophectoderm samples were diagnosed using fluorescent in situ hybridization on chromosomes 9, 13, 15, 16, 17, 18, 21, 22, X, Y. For comparison of morphological characteristics and euploidy, was chosen a group of embryos (group B) with the amount of 121 blastocysts obtained from 213 oocytes, which were gotten from the donor programs of assisted reproductive technologies (ART). Group B was not subjected to donor oocyte cytoplasmic transfer procedure and studied on the above mentioned chromosomes. Statistical analysis was carried out using the criteria t, x^2 at a significance levels p<0.05, p<0.01, p<0.001. Results: After the donor cytoplasm transfer process the amount of the third day developing embryos was 27 (79.4%). In this stage, the group B consisted of 189 (88.7%) developing embryos, and there was no statistically significant difference (SSD) between the two groups (p>0.05). After a comparative analysis of the morphological characteristics of the embryos on the fifth day, we also found no SSD among the studied groups (p>0.05): from 34 oocytes exposed to manipulation, 14 (41.2%) blastocysts was obtained, while the group B blastocyst yield was 56.8% (n=121) from 213 oocytes. The following results were obtained after PGS performing: in group A euploidy in studied chromosomes were 28.6%(n=4) blastocysts, whereas in group B this rate was 40.5%(n=49), 28.6%(n=4) and 21.5%(n=26) of mosaic embryos and 42.8%(n=6) and 38.0%(n=46) aneuploid blastocysts respectively were identified. None of these specified parameters had an SSD (p>0.05). But attention was drawn by the blastocysts in group A with identified mosaicism, which was chaotic without any cell having euploid chromosomal set, in contrast to the mosaic embryos in group B where identified chaotic mosaicism was only 2.5%(n=3). Conclusions: According to the obtained results, there is no direct procedural effect on the chromosome in embryos obtained following donor oocyte cytoplasmic transfer. Thus, the technology introduction will enhance the infertility treating effectiveness as well as avoiding having a child with mitochondrial disease. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=donor%20oocyte%20cytoplasmic%20transfer" title="donor oocyte cytoplasmic transfer">donor oocyte cytoplasmic transfer</a>, <a href="https://publications.waset.org/abstracts/search?q=embryos%E2%80%99%20chromosome%20set" title=" embryos’ chromosome set"> embryos’ chromosome set</a>, <a href="https://publications.waset.org/abstracts/search?q=oocyte%20spindle%20transfer" title=" oocyte spindle transfer"> oocyte spindle transfer</a>, <a href="https://publications.waset.org/abstracts/search?q=pronuclear%20transfer" title=" pronuclear transfer"> pronuclear transfer</a> </p> <a href="https://publications.waset.org/abstracts/57502/analysis-of-the-blastocysts-chromosomal-set-obtained-after-the-use-of-donor-oocyte-cytoplasmic-transfer-technology" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/57502.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">328</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">26</span> Evaluation of Developmental Toxicity and Teratogenicity of Perfluoroalkyl Compounds Using FETAX</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Hyun-Kyung%20Lee">Hyun-Kyung Lee</a>, <a href="https://publications.waset.org/abstracts/search?q=Jehyung%20Oh"> Jehyung Oh</a>, <a href="https://publications.waset.org/abstracts/search?q=Young%20Eun%20Jeong"> Young Eun Jeong</a>, <a href="https://publications.waset.org/abstracts/search?q=Hyun-Shik%20Lee"> Hyun-Shik Lee</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Perfluoroalkyl compounds (PFCs) are environmental toxicants that persistently accumulate in the human blood. Their widespread detection and accumulation in the environment raise concerns about whether these chemicals might be developmental toxicants and teratogens in the ecosystem. We evaluated and compared the toxicity of PFCs of containing various numbers of carbon atoms (C8-11 carbons) on vertebrate embryogenesis. We assessed the developmental toxicity and teratogenicity of various PFCs. The toxic effects on Xenopus embryos were evaluated using different methods. We measured teratogenic indices (TIs) and investigated the mechanisms underlying developmental toxicity and teratogenicity by measuring the expression of organ-specific biomarkers such as xPTB (liver), Nkx2.5 (heart), and Cyl18 (intestine). All PFCs that we tested were found to be developmental toxicants and teratogens. Their toxic effects were strengthened with increasing length of the fluorinated carbon chain. Furthermore, we produced evidence showing that perfluorodecanoic acid (PFDA) and perfluoroundecanoic acid (PFuDA) are more potent developmental toxicants and teratogens in an animal model compared to the other PFCs we evaluated [perfluorooctanoic acid (PFOA) and perfluorononanoic acid (PFNA)]. In particular, severe defects resulting from PFDA and PFuDA exposure were observed in the liver and heart, respectively, using the whole mount in situ hybridization, real-time PCR, pathologic analysis of the heart, and dissection of the liver. Our studies suggest that most PFCs are developmental toxicants and teratogens, however, compounds that have higher numbers of carbons (i.e., PFDA and PFuDA) exert more potent effects. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=PFC" title="PFC">PFC</a>, <a href="https://publications.waset.org/abstracts/search?q=xenopus" title=" xenopus"> xenopus</a>, <a href="https://publications.waset.org/abstracts/search?q=fetax" title=" fetax"> fetax</a>, <a href="https://publications.waset.org/abstracts/search?q=development" title=" development"> development</a> </p> <a href="https://publications.waset.org/abstracts/46966/evaluation-of-developmental-toxicity-and-teratogenicity-of-perfluoroalkyl-compounds-using-fetax" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/46966.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">352</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">25</span> Morphological Interaction of Porcine Oocyte and Cumulus Cells Study on in vitro Oocyte Maturation Using Electron Microscopy </h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=M.%20Areekijseree">M. Areekijseree</a>, <a href="https://publications.waset.org/abstracts/search?q=W.%20Pongsawat"> W. Pongsawat</a>, <a href="https://publications.waset.org/abstracts/search?q=M.%20Pumipaiboon"> M. Pumipaiboon</a>, <a href="https://publications.waset.org/abstracts/search?q=C.%20Thepsithar"> C. Thepsithar</a>, <a href="https://publications.waset.org/abstracts/search?q=S.%20Sengsai"> S. Sengsai</a>, <a href="https://publications.waset.org/abstracts/search?q=T.%20Chuen-Im"> T. Chuen-Im</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Morphological interaction of porcine cumulus-oocyte complexes (pCOCs) was investigated on in vitro condition using electron microscope (SEM and TEM). The totals of 1,923 oocytes were round in shape, surrounded by zona pellucida with layer of cumulus cells ranging between 59.29-202.14 µm in size. They were classified into intact-, multi-, partial cumulus cell layer oocyte, and completely denuded oocyte, at the percentage composition of 22.80% 32.70%, 18.60%, and 25.90 % respectively. The pCOCs classified as intact- and multi cumulus cell layer oocytes were further culturing at 37°C with 5% CO2, 95% air atmosphere and high humidity for 44 h in M199 with Earle’s salts supplemented with 10% HTFCS, 2.2 mg/mL NaHCO3, 1 M Hepes, 0.25 mM pyruvate, 15 µg/mL porcine follicle-stimulating hormone, 1 µg/mL LH, 1µg/mL estradiol with ethanol, and 50 µg/mL gentamycin sulfate. On electron microscope study, cumulus cells were found to stick their processes to secrete substance from the sac-shape end into zona pellucida of the oocyte and also communicated with the neighboring cells through their microvilli on the beginning of incubation period. It is believed that the cumulus cells communicate with the oocyte by inserting the microvilli through this gap and embedded in the oocyte cytoplasm before secreting substance, through the sac-shape end of the microvilli, to inhibit primary oocyte development at the prophase I. Morphological changes of the complexes were observed after culturing for 24-44 h. One hundred percentages of the cumulus layers were expanded and cumulus cells were peeling off from the oocyte surface. In addition, the round-shape cumulus cells transformed themselves into either an elongate shape or a columnar shape, and no communication between cumulus neighboring cells. After 44 h of incubation time, diameter of oocytes surrounded by cumulus cells was larger than 0 h incubation. The effect of hormones in culture medium is exerted by their receptors present in porcine oocyte. It is likely that all morphological changes of the complexes after hormone treatment were to allow maturation of the oocyte. This study demonstrated that the association of hormones in M199 could promote porcine follicle activation in 44 h in vitro condition. This culture system should be useful for studying the regulation of early follicular growth and development, especially because these follicles represent a large source of oocytes that could be used in vitro for cell technology. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=cumulus%20cells" title="cumulus cells">cumulus cells</a>, <a href="https://publications.waset.org/abstracts/search?q=electron%20microscopy" title=" electron microscopy"> electron microscopy</a>, <a href="https://publications.waset.org/abstracts/search?q=in%20vitro" title=" in vitro"> in vitro</a>, <a href="https://publications.waset.org/abstracts/search?q=porcine%20oocyte" title=" porcine oocyte"> porcine oocyte</a> </p> <a href="https://publications.waset.org/abstracts/20534/morphological-interaction-of-porcine-oocyte-and-cumulus-cells-study-on-in-vitro-oocyte-maturation-using-electron-microscopy" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/20534.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">385</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">24</span> Impact of Different Ripening Accelerators on the Microbial Load and Proximate Composition of Plantain (Musa paradisiaca) and Banana (Musa sapientum), during the Ripening Process, and the Nutrition Implication for Food Security</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Wisdom%20Robert%20Duruji">Wisdom Robert Duruji</a>, <a href="https://publications.waset.org/abstracts/search?q=Oluwasegun%20Christopher%20Akinleye"> Oluwasegun Christopher Akinleye</a> </p> <p class="card-text"><strong>Abstract:</strong></p> This study reports on the impact of different ripening accelerators on the microbial load and proximate composition of plantain (Musa paradisiaca) and Banana (Musa sapientum) during the ripening process, and the nutrition implication for food security. The study comprised of four treatments, namely: Calcium carbide, Irvingia gabonensis fruits, Newbouldia laevis leaves and a control, where no ripening accelerator was applied to the fingers of plantain and banana. The unripe and ripened plantain and banana were subjected to microbial analysis by isolating and enumerating their micro flora using pour plate method; and also, their proximate composition was determined using standard methods. The result indicated that the bacteria count of plantain increased from 3.25 ± 0.33 for unripe to 5.31 ± 0.30 log cfu/g for (treated) ripened, and that of banana increased from 3.69 ± 0.11 for unripe to 5.26 ± 0.21 log cfu/g for ripened. Also, the fungal count of plantain increased from 3.20 ± 0.16 for unripe to 4.88 ± 0.22 log sfu/g for ripened; and that of banana increased from 3.61 ± 0.19 for unripe to 5.43 ± 0.26 for ripened. Ripened plantain fingers without any ripening accelerator (control) had significantly (p < 0.05) higher values of crude protein 3.56 ± 0.06%, crude fat 0.42 ± 0.04%, total ash 2.74 ± 0.15 and carbohydrate 31.10 ± 0.20; but with significantly lower value of moisture 62.14 ± 0.07% when compared with treated plantain. The proximate composition trend of treated and banana fingers control is similar to that of treated and plantain control, except that higher moisture content of 75.11 ± 0.07% and lesser protein, crude fat, total ash and carbohydrate were obtained from treated and ripened banana control when the treatments were compared with that of plantain. The study concluded that plantain is more nutritious (mealy) than a banana; also, the ripening accelerators increased the microbial load and reduced the nutritional status of plantain and banana. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=food%20nutrition" title="food nutrition">food nutrition</a>, <a href="https://publications.waset.org/abstracts/search?q=calcium%20carbide" title=" calcium carbide"> calcium carbide</a>, <a href="https://publications.waset.org/abstracts/search?q=rvingia%20gabonensis" title=" rvingia gabonensis"> rvingia gabonensis</a>, <a href="https://publications.waset.org/abstracts/search?q=newbouldia%20laevis" title=" newbouldia laevis"> newbouldia laevis</a>, <a href="https://publications.waset.org/abstracts/search?q=plantain" title=" plantain"> plantain</a>, <a href="https://publications.waset.org/abstracts/search?q=banana" title=" banana"> banana</a> </p> <a href="https://publications.waset.org/abstracts/48032/impact-of-different-ripening-accelerators-on-the-microbial-load-and-proximate-composition-of-plantain-musa-paradisiaca-and-banana-musa-sapientum-during-the-ripening-process-and-the-nutrition-implication-for-food-security" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/48032.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">323</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">23</span> Influence of JHA and Ecdysteroid on Reproduction in Dysdercus similis (Hemiptera: Pyrrhocoridae)</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Versha%20Sharma">Versha Sharma</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Juvenile hormone analogue, fenoxycarb and ecdysterone, when applied at varying concentrations in the adult females of Dysdercus similis, in situ histochemical observations of treated ovarian and adipose tissues during the first gonotrophic cycle elicited drastic histomorphological changes in both tissues. The action and effect of both JHa and ecdysterone on ovarian development, vitellogenesis, the activity of follicular epithelium, chorion formation all were monitored in detail. SDS-PAGE electrophoretic analysis showed drastic downregulation on the protein profile of differently treated tissue samples. After exogenous JHa supply, resorption of the developing oocytes was also often noticed. Gradational decline and disappearance of different protein bands in treated both ovarian and adipose tissues noticed could be due to the depletion of specific metabolites essential for oocyte development and maturation. Natural products support both crop production and the environment that being effective in pest control, less toxic to non-target organisms and at the same time biodegradable. Hence, these could be utilized as an attractive alternative to the synthetic chemical insecticides for at least cotton bug pest management. Increasing IGR dosages is found to elicit both qualitative and quantitative depletion of protein metabolites and drastic histochemical changes in the gonads of the treated forms brought forth the production of a large number of immature mal-formed oocytes. Findings in greater detail could be discussed. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=juvenile%20hormone" title="juvenile hormone">juvenile hormone</a>, <a href="https://publications.waset.org/abstracts/search?q=ecdysone" title=" ecdysone"> ecdysone</a>, <a href="https://publications.waset.org/abstracts/search?q=P.%20picta" title=" P. picta"> P. picta</a>, <a href="https://publications.waset.org/abstracts/search?q=Dysdercus%20similis" title=" Dysdercus similis"> Dysdercus similis</a> </p> <a href="https://publications.waset.org/abstracts/5543/influence-of-jha-and-ecdysteroid-on-reproduction-in-dysdercus-similis-hemiptera-pyrrhocoridae" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/5543.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">252</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">22</span> Influence of Different Ripening Agents on the Shelf-Life and Microbial Load of Organic and Inorganic Musaceae, during the Ripening Process, and the Health Implication for Food Security</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Wisdom%20Robert%20Duruji">Wisdom Robert Duruji</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Local farmers and fruit processors in developing countries of West Africa use different ripening agents to accelerate the ripening process of plantain and banana. This study reports on the influence of different ripening agents on the shelf-life and microbial load of organic and inorganic plantain (Musa paradisiaca) and banana (Musa sapientum) during ripening process and the health implication for food security in Nigeria. The experiment consisted of four treatments, namely: Calcium carbide, Irvingia gabonensis fruits, Newbouldia laevis leaves and a control, where no ripening agent was applied to the fingers of plantain and banana. The unripe and ripened plantain and banana were subjected to microbial analysis by isolating their micro flora (Bacteria, Yeast and Mould) using pour plate method. Microbes present in the samples were enumerated, characterized and classified to genera and species. The result indicated that the microbial load of inorganic plantain from (Urban day) open market in Ile-Ife increased from 8.00 for unripe to 12.11 cfu/g for ripened; and the microbial load of organic plantain from Obafemi Awolowo University Teaching and Research Farm (OAUTRF) increased from 6.00 for unripe to 11.60 cfu/g for ripened. Also, the microbial load of inorganic banana from (Urban day) open market in Ile-Ife increased from 8.00 for unripe to 11.50 cfu/g for ripened; while the microbial load of organic banana from OAUTRF increased from 6.50 for unripe to 9.40 cfu/g for ripened. The microbial effects of the ripening agents increased from 10.00 for control to 16.00 cfu/g for treated (ripened) organic and inorganic plantain; while that of organic and inorganic banana increased from 7.50 for control to 14.50 cfu/g for ripened. Visual observation for the presence of fungal colonies and deterioration rates were monitored till seven days after the plantain and banana fingers have fully ripened. Inorganic plantain and banana from (Urban day) open market in Ile-Ife are more contaminated than organic plantain and banana fingers from OAUTRF. The ripening accelerators reduced the shelf life, increased senescence, and microbial load of plantain and banana. This study concluded that organic Agriculture is better and microbial friendlier than inorganic farming. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=organic%20agriculture" title="organic agriculture">organic agriculture</a>, <a href="https://publications.waset.org/abstracts/search?q=food%20security" title=" food security"> food security</a>, <a href="https://publications.waset.org/abstracts/search?q=Musaceae" title=" Musaceae"> Musaceae</a>, <a href="https://publications.waset.org/abstracts/search?q=calcium%20carbide" title=" calcium carbide"> calcium carbide</a>, <a href="https://publications.waset.org/abstracts/search?q=Irvingia%20gabonensis" title=" Irvingia gabonensis"> Irvingia gabonensis</a>, <a href="https://publications.waset.org/abstracts/search?q=Newbouldia%20laevis" title=" Newbouldia laevis"> Newbouldia laevis</a> </p> <a href="https://publications.waset.org/abstracts/45640/influence-of-different-ripening-agents-on-the-shelf-life-and-microbial-load-of-organic-and-inorganic-musaceae-during-the-ripening-process-and-the-health-implication-for-food-security" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/45640.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">584</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">21</span> Sublethal Effect of Tebufenozide, an Ecdysteroid Agonist, on the Reproduction of German Cockroach (Blattodea: Blattellidae)</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Samira%20Kilani-Morakchi">Samira Kilani-Morakchi</a>, <a href="https://publications.waset.org/abstracts/search?q=Amina%20Badi"> Amina Badi</a>, <a href="https://publications.waset.org/abstracts/search?q=Nadia%20Aribi"> Nadia Aribi </a> </p> <p class="card-text"><strong>Abstract:</strong></p> German cockroach, Blattella germanica, is known to be an important pest due to its high reproductive potential and its ability to build up large infectious populations. The infestations were generally controlled by neurotoxic insecticides including organophosphates (OP), carbamate and pyrethroids. An alternative cockroach’s control approach is the use insect growth regulators (IGRs). The relative fewer effects of these chemicals on non-target insects and animals, and their favourable environmental fate, make them attractive insecticides for inclusion in integrated pest management programmes. The juvenoids and chitin synthesis inhibitors are two classes of IGRs that have received the most attention for useful chemicals to manage German cockroaches while ecdysone agonists were mostly used to control Lepidopteran species. In the present study, the sublethal effects of the non-sreroidal ecdysone agonist tebufenozide were evaluated topically on adults of the B. germanica. The effects on reproduction were observed in adults females of cockroaches that survived exposure to LD25 (146 µg/g of insect) of tebufenozide. Dissection of treated females showed a clear reduction in both the number of oocytes per paired ovaries and the size of basal oocytes, as compared to controls. In addition, tebufenozide significantly reduced the mating success of pairs and altered the fertility as shown through the reduction of ootheca development and total absence of viable nymph. Tebufenozide disrupted the German cockroach reproduction by interfering with homeostasis of the insect hormones. In conclusion, the overall results suggested that tebufenozide can be used as a biorational insecticide for controlling cockroaches. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=B.%20germanica" title="B. germanica">B. germanica</a>, <a href="https://publications.waset.org/abstracts/search?q=ecdysteroid%20agonist" title=" ecdysteroid agonist"> ecdysteroid agonist</a>, <a href="https://publications.waset.org/abstracts/search?q=tebufenozide" title=" tebufenozide"> tebufenozide</a>, <a href="https://publications.waset.org/abstracts/search?q=reproduction" title=" reproduction"> reproduction</a> </p> <a href="https://publications.waset.org/abstracts/31258/sublethal-effect-of-tebufenozide-an-ecdysteroid-agonist-on-the-reproduction-of-german-cockroach-blattodea-blattellidae" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/31258.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">296</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">20</span> Pyrroloquinoline Quinone Enhances the Mitochondrial Function by Increasing Beta-Oxidation and a Balanced Mitochondrial Recycling in Mice Granulosa Cells</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Moustafa%20Elhamouly">Moustafa Elhamouly</a>, <a href="https://publications.waset.org/abstracts/search?q=Masayuki%20Shimada"> Masayuki Shimada</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The production of competent oocytes is essential for reproductivity in mammals. Maintenance of mitochondrial efficiency is required to supply the ATP necessary for granulosa cell proliferation during the follicular development process. Treatment with Pyrroloquinoline quinone (PQQ) has been reported to increase the number of ovulated oocytes and pups per delivery in mice by maintaining healthy mitochondrial function. This study aimed to elucidate how PQQ maintains mitochondrial function during ovarian follicle growth. To do this, both in vitro and in vivo experiments were performed with granulosa cells from superovulated immature (3-week-old) mice that were pretreated with or without PQQ. The effects of PQQ on beta-oxidation, mitochondrial function, mitophagy, and mitochondrial biogenesis were examined. PQQ increased beta-oxidation-related genes and CPT1 protein content in granulosa cells and this was associated with a decreased phosphorylation of P38 signaling protein. Using the fatty acid oxidation assay on the flux analyzer, PQQ increased the reliance of beta-oxidation on the endogenous fatty acids and was associated with a mild UCP-dependant mitochondrial uncoupling, ATP production, mitophagy, and mitochondrial biogenesis. PQQ also increased the expression of endogenous antioxidant enzymes. Thus, PQQ induced beta-oxidation in growing granulosa cells relying on endogenous fatty acids. And reduced the Reactive oxygen species (ROS) production by inducing a mild mitochondrial uncoupling with keeping high mitochondrial function. Damaged mitochondria were recycled by the induced mitophagy and replaced by the increased mitochondrial biogenesis. Collectively, PQQ may enhance reproductivity by maintaining the efficiency of mitochondria to produce enough ATP required for normal folliculogenesis. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=granulosa%20cells" title="granulosa cells">granulosa cells</a>, <a href="https://publications.waset.org/abstracts/search?q=mitochondrial%20uncoupling" title=" mitochondrial uncoupling"> mitochondrial uncoupling</a>, <a href="https://publications.waset.org/abstracts/search?q=mitophagy" title=" mitophagy"> mitophagy</a>, <a href="https://publications.waset.org/abstracts/search?q=pyrroloquinoline%20quinone%20%28PQQ%29" title=" pyrroloquinoline quinone (PQQ)"> pyrroloquinoline quinone (PQQ)</a>, <a href="https://publications.waset.org/abstracts/search?q=reactive%20oxygen%20species%20%28ROS%29." title=" reactive oxygen species (ROS)."> reactive oxygen species (ROS).</a> </p> <a href="https://publications.waset.org/abstracts/156680/pyrroloquinoline-quinone-enhances-the-mitochondrial-function-by-increasing-beta-oxidation-and-a-balanced-mitochondrial-recycling-in-mice-granulosa-cells" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/156680.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">82</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">19</span> Enhancing Mitochondrial Activity and Metabolism in Aging Female Germ Cells: Synergistic Effects of Dual ROCK and ROS Inhibition</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Kuan-Hao%20Tsui">Kuan-Hao Tsui</a>, <a href="https://publications.waset.org/abstracts/search?q=Li-Te%20Lin"> Li-Te Lin</a>, <a href="https://publications.waset.org/abstracts/search?q=Chia-Jung%20Li"> Chia-Jung Li</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The combination of Y-27632 and Vitamin C significantly enhances the quality of aging germ cells by reducing reactive oxygen species (ROS) production, restoring mitochondrial membrane potential balance, and promoting mitochondrial fusion. The age-related decline in oocyte quality contributes to reduced fertility, increased aneuploidy, and diminished embryo quality, with mitochondrial dysfunction in both oocytes and granulosa cells being a key factor in this decline. Experiments on aging germ cells investigated the effects of the Y-27632 and Vitamin C combination. In vivo studies involved aged mice to assess oocyte maturation and ROS accumulation during culture. The assessment included mitochondrial activity, ROS levels, mitochondrial membrane potential, and mitochondrial dynamics. Cellular energy metabolism and ATP production were also measured. The combination treatment effectively addressed mitochondrial dysfunction and regulated cellular energy metabolism, promoting oxygen respiration and increasing ATP production. In aged mice, this supplement treatment enhanced in vitro oocyte maturation and prevented ROS accumulation in aging oocytes during culture. While these findings are promising, further research is needed to explore the long-term effects and potential side effects of the Y-27632 and Vitamin C combination. Additionally, translating these findings to human subjects requires careful consideration. Overall, the study suggests that the Y-27632 and Vitamin C combination could be a promising intervention to mitigate aging-related dysfunction in germ cells, potentially enhancing oocyte quality, particularly in the context of in vitro fertilization. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=ovarian%20aging" title="ovarian aging">ovarian aging</a>, <a href="https://publications.waset.org/abstracts/search?q=supplements" title=" supplements"> supplements</a>, <a href="https://publications.waset.org/abstracts/search?q=ROS" title=" ROS"> ROS</a>, <a href="https://publications.waset.org/abstracts/search?q=mitochondria" title=" mitochondria"> mitochondria</a> </p> <a href="https://publications.waset.org/abstracts/186480/enhancing-mitochondrial-activity-and-metabolism-in-aging-female-germ-cells-synergistic-effects-of-dual-rock-and-ros-inhibition" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/186480.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">40</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">18</span> Selection of Developmental Stages of Bovine in vitro-Derived Blastocysts Prior to Vitrification and Embryo Transfer: Implications for Cattle Breeding Programs</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Van%20Huong%20Do">Van Huong Do</a>, <a href="https://publications.waset.org/abstracts/search?q=Simon%20Walton"> Simon Walton</a>, <a href="https://publications.waset.org/abstracts/search?q=German%20Amaya"> German Amaya</a>, <a href="https://publications.waset.org/abstracts/search?q=Madeline%20Batsiokis"> Madeline Batsiokis</a>, <a href="https://publications.waset.org/abstracts/search?q=Sally%20Catt"> Sally Catt</a>, <a href="https://publications.waset.org/abstracts/search?q=Andrew%20Taylor-Robinson"> Andrew Taylor-Robinson</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Identification of the most suitable stages of bovine in vitro-derived blastocysts (early, expanded and hatching) prior to vitrification is a straightforward process that facilitates the decision as to which blastocyst stage to use for transfer of fresh and vitrified embryos. Research on in vitro evaluation of suitable stages has shown that the more advanced developmental stage of blastocysts is recommended for fresh embryo transfer while the earlier stage is proposed for embryo transfer following vitrification. There is, however, limited information on blastocyst stages using in vivo assessment. Hence, the aim of the present study was to determine the optimal stage of a blastocyst for vitrification and embryo transfer through a two-step procedure of embryo transfer followed by pregnancy testing at 35, 60 and 90 days of pregnancy. 410 good quality oocytes aspirated by the ovum pick-up technique from 8 donor cows were subjected to in vitro embryo production, vitrification and embryo transfer. Good quality embryos were selected, subjected to vitrification and embryo transfer. Subsequently, 77 vitrified embryos at different blastocyst stages were transferred to synchronised recipient cows. The overall cleavage and blastocyst rates of oocytes were 68.8% and 41.7%, respectively. In addition, the fertility and blastocyst production of 6 bulls used for in vitro fertilization was examined and shown to be statistically different (P<0.05). Results of ongoing pregnancy trials conducted at 35 days, 60 days and 90 days will be discussed. However, preliminary data indicate that individual bulls demonstrate distinctly different fertility performance in vitro. Findings from conception rates would provide a useful tool to aid selection of bovine in vitro-derived embryos for vitrification and embryo transfer in commercial settings. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=blastocyst" title="blastocyst">blastocyst</a>, <a href="https://publications.waset.org/abstracts/search?q=embryo%20transfer" title=" embryo transfer"> embryo transfer</a>, <a href="https://publications.waset.org/abstracts/search?q=in%20vitro-derived%20embryos" title=" in vitro-derived embryos"> in vitro-derived embryos</a>, <a href="https://publications.waset.org/abstracts/search?q=ovum%20pick-up" title=" ovum pick-up"> ovum pick-up</a>, <a href="https://publications.waset.org/abstracts/search?q=vitrification" title=" vitrification"> vitrification</a> </p> <a href="https://publications.waset.org/abstracts/78837/selection-of-developmental-stages-of-bovine-in-vitro-derived-blastocysts-prior-to-vitrification-and-embryo-transfer-implications-for-cattle-breeding-programs" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/78837.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">306</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">17</span> Ideas About Varroa Destructor Reproduction in the Honey Bees (Hymenoptera: Apidae)</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=William%20Ramirez-Benavides">William Ramirez-Benavides</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The mite Varroa destructor Anderson & Trueman (Mesostigmata: Varroidae), is an exclusive hematophagous parasite of the Apis honey bees (Apidae: Hymenoptera). The early phoretic female mites have multiple small inactivated oocytes. Consequently, for the initial growth and vitellogenesis of the oocytes, the mother mite must feed on the hemolymph of the host, as a unique food source, by taking intermittently variable number of blood meals: 1. During the phoretic phase, to initiate vitellogenesis of the terminal oocyte, 2. From a freshly capped bee cell with a bee larva, up to the apolysis stage, to complete vitellogenesis and embryogenesis of the terminal oocyte, and 3. From all pupal stages, up to the imago stage, to induce oogenesis and vitellogenesis of the would-be nonembryonic female eggs. Additionally, oogenesis and vitellogenesis expressions in Varroa destructor and other Varroidae varies according to environmental conditions, e.g., chemical attractions produced by the adult bee and larvae, race of bees, sex of the larva, developmental period of the bee larva, food quality and quantity, and superparasitism (several cofoundressess). Also, the feeding stimuli obtained from the host hemolymph, indirectly regulate the reproductive physiology of the mite, by inducing different vitellogenin expressions, the production of a male egg first in the sequence followed by vitellogenesis of the would-be female eggs during the pupal stages. Furthermore, the different uptakes of hemolymph from the host, also indirectly induce the production of the male egg first in the sequence, local mate competition (LMC) and variable adaptive female sex ratios in the broods, especially when superparasitism occurs. Consequently, reproduction in Varroa destructor, and probably in other Varroidae, depends exclusively on feeding in the hemolymph of the bee host, even during the phoretic phase, the prepupal stages and during the pupal stages; and that, the feeding factors are common syndromes in other Varroidae. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=oogenesis" title="oogenesis">oogenesis</a>, <a href="https://publications.waset.org/abstracts/search?q=sex%20determination" title=" sex determination"> sex determination</a>, <a href="https://publications.waset.org/abstracts/search?q=varroa%20destructor" title=" varroa destructor"> varroa destructor</a>, <a href="https://publications.waset.org/abstracts/search?q=vitellogenesis" title=" vitellogenesis"> vitellogenesis</a> </p> <a href="https://publications.waset.org/abstracts/191368/ideas-about-varroa-destructor-reproduction-in-the-honey-bees-hymenoptera-apidae" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/191368.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">16</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">16</span> The Phylogenetic Investigation of Candidate Genes Related to Type II Diabetes in Man and Other Species</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Srijoni%20Banerjee">Srijoni Banerjee</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Sequences of some of the candidate genes (e.g., CPE, CDKAL1, GCKR, HSD11B1, IGF2BP2, IRS1, LPIN1, PKLR, TNF, PPARG) implicated in some of the complex disease, e.g. Type II diabetes in man has been compared with other species to investigate phylogenetic affinity. Based on mRNA sequence of these genes of 7 to 8 species, using bioinformatics tools Mega 5, Bioedit, Clustal W, distance matrix was obtained. Phylogenetic trees were obtained by NJ and UPGMA clustering methods. The results of the phylogenetic analyses show that of the species compared: Xenopus l., Danio r., Macaca m., Homo sapiens s., Rattus n., Mus m. and Gallus g., Bos taurus, both NJ and UPGMA clustering show close affinity between clustering of Homo sapiens s. (Man) with Rattus n. (Rat), Mus m. species for the candidate genes, except in case of Lipin1 gene. The results support the functional similarity of these genes in physiological and biochemical process involving man and mouse/rat. Therefore, in understanding the complex etiology and treatment of the complex disease mouse/rate model is the best laboratory choice for experimentation. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=phylogeny" title="phylogeny">phylogeny</a>, <a href="https://publications.waset.org/abstracts/search?q=candidate%20gene%20of%20type-2%20diabetes" title=" candidate gene of type-2 diabetes"> candidate gene of type-2 diabetes</a>, <a href="https://publications.waset.org/abstracts/search?q=CPE" title=" CPE"> CPE</a>, <a href="https://publications.waset.org/abstracts/search?q=CDKAL1" title=" CDKAL1"> CDKAL1</a>, <a href="https://publications.waset.org/abstracts/search?q=GCKR" title=" GCKR"> GCKR</a>, <a href="https://publications.waset.org/abstracts/search?q=HSD11B1" title=" HSD11B1"> HSD11B1</a>, <a href="https://publications.waset.org/abstracts/search?q=IGF2BP2" title=" IGF2BP2"> IGF2BP2</a>, <a href="https://publications.waset.org/abstracts/search?q=IRS1" title=" IRS1"> IRS1</a>, <a href="https://publications.waset.org/abstracts/search?q=LPIN1" title=" LPIN1"> LPIN1</a>, <a href="https://publications.waset.org/abstracts/search?q=PKLR" title=" PKLR"> PKLR</a>, <a href="https://publications.waset.org/abstracts/search?q=TNF" title=" TNF"> TNF</a>, <a href="https://publications.waset.org/abstracts/search?q=PPARG" title=" PPARG"> PPARG</a> </p> <a href="https://publications.waset.org/abstracts/5222/the-phylogenetic-investigation-of-candidate-genes-related-to-type-ii-diabetes-in-man-and-other-species" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/5222.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">321</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">15</span> Importance of Cryptosporidiosis in Dairy Calves</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Mohammad%20Asadpour">Mohammad Asadpour</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Cryptosporidium spp. is zoonotic pathogens transmissible from a variety of animals to humans and is a considerable public health concern. Calves have been identified in numerous reports as a major source of environmental contamination with this pathogen. Parasite has a different species that are the cases of zoonotic disease in immunodeficient people and neonatal calves. Cryptosporidium oocysts are extremely resistant to chlorine and other physical cases that commonly used in drinking water. Reproduction of resistant oocytes is a way for this monoxenous parasite to remain in the environment. Cryptosporidium parvum is the most important species that has human and cattle genotypes. Cryptosporidium is one of the most important causes of diarrhea in neonatal calves and also, one of the four causes of diarrhea symptoms in pre-weaned calves. Because of the incompetent immune system in calves, Cryptosporidium infection is the cause of a lot of problems in raising farms. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Cryptosporidium%20spp" title="Cryptosporidium spp">Cryptosporidium spp</a>, <a href="https://publications.waset.org/abstracts/search?q=dairy%20calves" title=" dairy calves"> dairy calves</a>, <a href="https://publications.waset.org/abstracts/search?q=importance" title=" importance"> importance</a>, <a href="https://publications.waset.org/abstracts/search?q=veterinary%20medicine" title=" veterinary medicine"> veterinary medicine</a> </p> <a href="https://publications.waset.org/abstracts/5549/importance-of-cryptosporidiosis-in-dairy-calves" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/5549.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">583</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">14</span> Effects of Tramadol Administration on the Ovary of Adult Rats and the Possible Recovery after Tramadol Withdrawal: A Light and Electron Microscopic Study </h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Heba%20Kamal%20Mohamed">Heba Kamal Mohamed</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Introduction: Tramadol is a weak -opioid receptor agonist with an analgesic effect because of the inhibition of uptake of norepinephrine and serotonin. Nowadays, tramadol hydrochloride is frequently used as a pain reliever. Tramadol is recommended for the management of acute and chronic pain of moderate to severe intensity associated with a variety of diseases or problems, including osteoarthritis, diabetic neuropathy, neuropathic pain, and even perioperative pain in human patients. In obstetrics and gynecology, tramadol is used extensively to treat postoperative pain. Aim of the study: This study was undertaken to investigate the histological (light and electron microscopic) and immunohistochemical effects of long term tramadol treatment on the ovary of adult rats and the possible recovery after tramadol withdrawal. Design: Experimental study. Materials and methods: Thirty adult female albino rats were used in this study. They were classified into three main groups (10 rats each). Group I served as the control group. Group II, rats were subcutaneously injected with tramadol 40 mg/kg three times per week for 8 weeks. Group III, rats were subcutaneously injected with tramadol 40 mg/kg three times per week for 8 weeks then were kept for another 8 weeks without treatment for recovery. At the end of the experiment rats were sacrificed and bilateral oophorectomy was carried out; the ovaries were processed for histological study (light and electron microscopic) and immunohistochemical reaction for caspase-3 (apoptotic protein). Results: Examination of the ovary of tramadol-treated rats (group II) revealed many atretic ovarian follicles, some follicles showed detachment of the oocyte from surrounding granulosa cells and others showed loss of the oocyte. Many follicles revealed degenerated vacuolated oocytes and vacuolated theca folliculi cells. Granulosa cells appeared shrunken, disrupted and loosely attached with vacuolated cytoplasm and pyknotic nuclei. Some follicles showed separation of granulosa cells from the theca folliculi layer. The ultrastructural study revealed the presence of granulosa cells with electron dense indented nuclei, damaged mitochondria and granular vacuolated cytoplasm. Other cells showed accumulation of large amount of lipid droplets in their cytoplasm. Some follicles revealed rarifaction of the cytoplasm of oocytes and absent zona pellucida. Moreover, apoptotic changes were detected by immunohistochemical staining in the form of increased staining intensity to caspase-3 (apoptotic protein). With Masson's Trichrome stain, there was an increased collagen fibre deposition in the ovarian cortical stroma. The wall of blood vessels appeared thickened. In the withdrawal group (group III), there was a little improvement in the histological and immunohistochemical changes. Conclusion: Tramadol had serious deleterious effects on ovarian structure. Thus, it should be used with caution, especially when a long term treatment is indicated. Withdrawal of tramadol led to a little improvement in the structural impairment of the ovary. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=tramadol" title="tramadol">tramadol</a>, <a href="https://publications.waset.org/abstracts/search?q=ovary" title=" ovary"> ovary</a>, <a href="https://publications.waset.org/abstracts/search?q=withdrawal" title=" withdrawal"> withdrawal</a>, <a href="https://publications.waset.org/abstracts/search?q=rats" title=" rats"> rats</a> </p> <a href="https://publications.waset.org/abstracts/26991/effects-of-tramadol-administration-on-the-ovary-of-adult-rats-and-the-possible-recovery-after-tramadol-withdrawal-a-light-and-electron-microscopic-study" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/26991.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">293</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">13</span> The Role of Polar Body in the Female Gamete</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Parsa%20Sheikhzadeh">Parsa Sheikhzadeh</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Polar bodies are cells that form by oogenesis in meiosis which differentiate and develop from oocytes. Although in many animals, these cells often die following meiotic maturation of the oocyte. Oocyte activation is during mammalian fertilization, sperm is fused with the oocyte's membrane, triggering the resumption of meiosis from the metaphase II arrest, the extrusion of the second polar body, and the exocytosis of cortical granules. The origin recognition complex proteins 4 (ORC4) forms a cage around the set of chromosomes that will be extruded during polar body formation before it binds to the chromatin shortly before zygotic DNA replication. One unique feature of the female gamete is that the polar bodies can provide beneficial information about the genetic background of the oocyte without potentially destroying it. Testing at the polar body (PB) stage was the least accurate, mainly due to the high incidence of post-zygotic events. On the other hand, the results from PB1-MII oocyte pair validated that PB1 contains nearly the same methylome (average Pearson correlation is 0.92) with sibling MII oocyte. In this article, we comprehensively examine the role of polar bodies in female human gametes. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=polar%20bodies" title="polar bodies">polar bodies</a>, <a href="https://publications.waset.org/abstracts/search?q=ORC4" title=" ORC4"> ORC4</a>, <a href="https://publications.waset.org/abstracts/search?q=oocyte" title=" oocyte"> oocyte</a>, <a href="https://publications.waset.org/abstracts/search?q=genetic" title=" genetic"> genetic</a>, <a href="https://publications.waset.org/abstracts/search?q=methylome" title=" methylome"> methylome</a>, <a href="https://publications.waset.org/abstracts/search?q=gamete" title=" gamete"> gamete</a>, <a href="https://publications.waset.org/abstracts/search?q=female" title=" female"> female</a> </p> <a href="https://publications.waset.org/abstracts/169216/the-role-of-polar-body-in-the-female-gamete" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/169216.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">94</span> </span> </div> </div> <ul class="pagination"> <li class="page-item disabled"><span class="page-link">&lsaquo;</span></li> <li class="page-item active"><span class="page-link">1</span></li> <li class="page-item"><a class="page-link" href="https://publications.waset.org/abstracts/search?q=Xenopus%20laevis%20oocytes&page=2">2</a></li> <li class="page-item"><a class="page-link" href="https://publications.waset.org/abstracts/search?q=Xenopus%20laevis%20oocytes&page=2" rel="next">&rsaquo;</a></li> </ul> </div> </main> <footer> <div id="infolinks" class="pt-3 pb-2"> <div class="container"> <div style="background-color:#f5f5f5;" class="p-3"> <div class="row"> <div class="col-md-2"> <ul class="list-unstyled"> About <li><a href="https://waset.org/page/support">About 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