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Amphetamine Stimulation throughout Embryogenesis Promotes Long-lasting Epigenetic Modification in the Dopamine Transporter in Adult Animals
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justify-content-between"> <div class="col-12 col-sm-auto"> <p class="text-muted mb-0"> Perspective - (2023) Volume 7, Issue 4 </p> </div> <div class="col-12 col-sm-4 text-right"> <!-- <a href="https://www.hilarispublisher.com/open-access/amphetamine-stimulation-throughout-embryogenesis-promotes-longlasting-epigenetic-modification-in-the-dopamine-transporte.pdf" title="View PDF" class="btn btn-sm btn_cu_color rounded-50"><i class="fas fa-file-pdf"></i> View PDF</a> <a href="https://www.hilarispublisher.com/pdfdownload.php?download=open-access/amphetamine-stimulation-throughout-embryogenesis-promotes-longlasting-epigenetic-modification-in-the-dopamine-transporte.pdf&aid=101798" title="Download PDF" class="btn btn-sm btn_cu_color rounded-50"><i class="fas fa-download"></i> Download PDF</a> --> </div> </div> <h1 class="font-size-8 mt-2">Amphetamine Stimulation throughout Embryogenesis Promotes Long-lasting Epigenetic Modification in the Dopamine Transporter in Adult Animals</h1> <a href='https://www.hilarispublisher.com/author/rosemary-brecht-39791' title='Rosemary Brecht' style='color:#555; border-bottom:1px dotted #CCC;'>Rosemary Brecht</a><sup><a href='#Rosemary_Brecht'>*</a></sup> <!-- <div> </div> --> <br/> <div class="mb-2"></div> <a id="Rosemary_Brecht"></a> <strong><sup>*</sup>Correspondence:</strong> Rosemary Brecht, Department of Wildlife Resources, Utah State University, Logan, Utah, USA, <strong>Email:</strong> <i class='fa fa-envelope' aria-hidden='true' title='rose.mary@b.ac.edu'></i> <div class="clearfix mt-2 mb-3"> <div class="float-left"><a href="#ai" class="btn_cu_color" id="changeicon" data-toggle="collapse" data-target="#au_info"><strong>Author information</strong> <span><i class="fas fa-plus fa-sm"></i></span></a></div> <div class="float-right"> <nav class="nav a-mx-2 med_pdf"> <a 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</strong>04-Aug-2023, Pre QC No. P-114002; <strong>Reviewed: </strong>16-Aug-2023, QC No. Q-114002; <strong>Revised: </strong>21-Aug-2023, Manuscript No. R-114002; <strong>Published:</strong> 28-Aug-2023 , <strong>DOI:</strong> 10.37421/2952-8097.2023.7.205 <br> <strong>Citation:</strong> Brecht, Rosemary. “Amphetamine Stimulation throughout Embryogenesis Promotes Long-lasting Epigenetic Modification in the Dopamine Transporter in Adult Animals.” J Anim Health Behav Sci 7 (2023): 205. <br> <strong>Copyright:</strong> © 2023 Brecht R. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. </p> </div> </div> </div> <h4>Introduction</h4> <p>The use of amphetamine, a powerful stimulant has been a subject of extensive research and debate for decades due to its widespread recreational and medicinal use. One of the central mechanisms through which amphetamine exerts its effects is the modulation of dopamine neurotransmission in the brain. While much is known about the acute and chronic effects of amphetamine on the brain's reward system and its impact on behavior less attention has been given to the potential long-lasting consequences of amphetamine exposure during early development. Emerging research suggests that exposure to amphetamines during embryogenesis may lead to lasting epigenetic modifications in the Dopamine Transporter (DAT), a key protein responsible for regulating dopamine levels in the brain. This article explores the current state of knowledge regarding amphetamine-induced epigenetic modifications during embryogenesis their potential consequences in adult animals, and the broader implications for understanding addiction, neurodevelopmental disorders, and epigenetic mechanisms.</p> <h4>Description</h4> <p>Amphetamines, including methamphetamine and its derivatives, are known to readily cross the placenta and affect the developing embryo. In pregnant women who use amphetamines, these compounds can reach the developing foetus exposing it to their pharmacological effects. This early exposure has been linked to various adverse outcomes including preterm birth, low birth weight and developmental abnormalities. During embryogenesis, the epigenome undergoes dynamic changes that play a crucial role in shaping cellular identity and function. Epigenetic modifications, such as DNA methylation, histone modifications, and non-coding RNA regulation, can influence gene expression patterns thereby affecting developmental processes. It is within this context that amphetamine exposure during embryogenesis may exert its long-lasting effects on the developing brain [<a href="#1" title="1">1</a>].</p> <p>Recent research has uncovered evidence suggesting that amphetamine exposure during embryogenesis can lead to alterations in epigenetic marks within the dopaminergic system. Studies in animal models have demonstrated changes in DNA methylation patterns and histone modifications in genes related to dopamine signalling, including DAT. These epigenetic modifications are thought to persist into adulthood, potentially influencing the functioning of the dopaminergic system and related behaviors. The Dopamine Transporter (DAT) is a critical protein involved in the regulation of dopamine levels in the brain [<a href="#2" title="2">2</a>]. DAT is primarily responsible for the reuptake of extracellular dopamine into presynaptic neurons, thus terminating dopamine signalling and maintaining proper neurotransmission. Dysregulation of DAT function has been implicated in various neuropsychiatric disorders, including attention deficit hyperactivity disorder (ADHD) and substance use disorders.</p> <p>The DAT gene, also known as SLC6A3 encodes the DAT protein. The expression of DAT is tightly regulated to ensure precise control of dopamine reuptake. Epigenetic modifications, including DNA methylation and histone acetylation, play a pivotal role in modulating DAT gene expression. Changes in the epigenetic landscape of the DAT gene can lead to alterations in DAT protein levels, potentially influencing dopamine homeostasis in the brain. Dopaminergic signalling is essential for various cognitive and emotional functions, including reward processing, motivation and motor control. DAT by regulating dopamine reuptake modulates the duration and intensity of dopamine signalling at synapses [<a href="#3" title="3">3</a>]. Dysregulated DAT function can lead to aberrant dopamine levels, which are implicated in psychiatric disorders such as schizophrenia and addiction.</p> <p>Amphetamine exposure during embryogenesis has been associated with epigenetic modifications in the dopaminergic system. These modifications can impact DAT gene expression and function, potentially leading to lasting changes in dopamine signalling in adult animals. Studies have shown that amphetamine exposure during embryogenesis can lead to altered DNA methylation patterns in the promoter region of the DAT gene. Hyper methylation of the DAT promoter is associated with decreased gene expression, leading to reduced DAT protein levels. This reduction in DAT function may result in elevated extracellular dopamine levels, which could contribute to behavioral alterations seen in adult animals exposed to amphetamines in utero [<a href="#4" title="4">4</a>].</p> <p>In addition to DNA methylation, amphetamine exposure has been linked to changes in histone modifications within the dopaminergic system. Histone modifications, such as acetylation and methylation can influence chromatin accessibility and gene expression. Amphetamine-induced alterations in histone acetylation patterns may contribute to long-lasting changes in the expression of genes involved in dopamine signalling, including DAT. The epigenetic modifications induced by amphetamine exposure during embryogenesis can have profound behavioral consequences in adult animals. These consequences are mediated through alterations in the dopaminergic system, affecting reward processing, impulsivity, and susceptibility to substance abuse. Amphetamineinduced epigenetic modifications may lead to changes in reward circuitry in the brain. Altered DAT function can result in prolonged dopamine signaling at synapses, which may contribute to heightened sensitivity to rewarding stimuli. This increased reward sensitivity could predispose adult animals to seek out rewarding substances and behaviors, potentially increasing the risk of addiction [<a href="#5" title="5">5</a>].</p> <h4>Conclusion</h4> <p>Amphetamine exposure during embryogenesis can induce long-lasting epigenetic modifications in the Dopamine Transporter (DAT) and other components of the dopaminergic system. These modifications have significant implications for behavior in adult animals, including altered reward processing, increased impulsivity, and susceptibility to substance abuse. Understanding the epigenetic mechanisms underlying these effects provides valuable insights into addiction, neurodevelopmental disorders, and the developmental origins of behavioral dysfunction. Moreover, it opens up new avenues for therapeutic interventions aimed at mitigating the long-term consequences of early amphetamine exposure on the brain. Further research in this field promises to deepen our understanding of the complex interplay between early-life experiences, epigenetics, and brain function.</p> <h4>Acknowledgement</h4> <p>None.</p> <h4>Conflict of Interest</h4> <p>None.</p> <h4>References</h4> <ol> <li><a name="1" id="1"></a>Hansen, Freja H., Tina Skjørringe, Saiqa Yasmeen and Natascha V. 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</script> <script src="/assets/js/jquery.mCustomScrollbar.concat.min.js" type="text/javascript"></script> <script type="text/javascript"> // Scrollbar var Scrollbar = function() { "use strict"; // Handle Scrollbar Linear var handleScrollbarLinear = function() { $(".scrollbar").mCustomScrollbar({ theme: "minimal-dark" }); } return { init: function() { handleScrollbarLinear(); // initial setup for scrollbar linear } } }(); $(document).ready(function() { Scrollbar.init(); }); /*========================== Bootstrap Popover ============================*/ $(function () { $('[data-toggle="popover"]').popover() }) </script> <script src="/assets/js/jquery.malihu.PageScroll2id.min.js" type="text/javascript"></script> <script type="text/javascript">(function($){ $(window).on("load",function(){ $("a[rel='m_PageScroll2id']").mPageScroll2id(); }); })(jQuery); </script> <!------autosuggest search----> <!--<script type="text/javascript" src="/assets/js/coolautosuggest.js"></script> <script language="javascript" type="text/javascript"> $("#keyword").coolautosuggest({ url: "https://www.hilarispublisher.com/author-names.php?chars=", minChars: 3, }); </script> <!------onspot search----> <!--<script type="text/javascript"> $(document).ready(function() { $("#wait").hide(); $("#jkeyword").keyup(function() { $("#wait").show(); //values of sending variables var jkeyword=$("#jkeyword").val(); var dataString = { 'jkeyword':jkeyword }; $.ajax ({ type: "POST", url: "https://www.hilarispublisher.com/journal-search.php", data:dataString, cache: false, success: function(html) { $("#jresult").html(html); $("#wait").hide();} }); }); }); </script>--> <!--<style> .bell_icon { position: fixed; border-radius: 3px; right: 0px; bottom: 113px; color: #fff; z-index: 99999; } .bell_icon img { width: 100%; max-width: 160px; border-radius: 8px; } </style>--> <script type="text/javascript">function add_chatinline(){var hccid=93340644;var 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