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<ArticleSet><Article><Journal><PublisherName></PublisherName><JournalTitle>Journal of Research in Medical Sciences</JournalTitle><Issn>1735-1995</Issn><Volume>17</Volume><Issue>7</Issue><PubDate PubStatus="epublish"><Year>2012</Year><Month>05</Month><Day>15</Day></PubDate></Journal><ArticleTitle>Toxicity effects of methamphetamine on the embryonic stem cell-derived neuron</ArticleTitle><FirstPage>8311</FirstPage><LastPage>8311</LastPage><Language>EN</Language><AuthorList><Author><FirstName>Rokhsareh</FirstName><LastName>Meamar</LastName><Affiliation>Neuroscience Research Centre, Isfahan University of Medical Sciences And Department of Medical Science, Najaf Abad Branch, Islamic Azad University And Department of Cell and Molecular Biology, Cell Science Research Centre, Royan Institute for Animal Biote. meamar@pharm.mui.ac.ir</Affiliation></Author><Author><FirstName>Leila</FirstName><LastName>Dehghani</LastName></Author><Author><FirstName>Freshte</FirstName><LastName>Karamali</LastName></Author></AuthorList><History><PubDate PubStatus="received"><Year>2012</Year><Month>04</Month><Day>15</Day></PubDate><PubDate PubStatus="accepted"><Year>2012</Year><Month>05</Month><Day>15</Day></PubDate></History><Abstract>BACKGROUND: Methamphetamine (MA) is the most popular recreational drug. According to potential neurotoxicity of this agent, it can cause deleterious effects in neural differentiation of the embryo, if used during the child bearing period. In recent decades, undifferentiated pluripotent embryo-derived stem cell lines, resembling early embryonic stages, have been used to analyze the toxic effects of components in vitro. Thus, this study aims at assessing toxic effects of MA on embryonic stem cell (ESC)-derived neuronal cells during differentiation in a pharmacological model. METHODS: Royan ESC line was used throughout this study. The effect of MA on neural differentiation was assessed during two periods, group 1: MA (10, 100, 200,500, 750, 1000 &amp;micro;M concentrations) was added during EB formation, group 2: MA (10, 50, 70, 100, 200, 500 &amp;micro;M concentrations) was added after the generation of neural precursors. Then cells were evaluated for neuronal markers by immunocytochemistry and RT-PCR.&amp;nbsp; One way ANOVA followed by the post hoc test was used to analyze data. RESULTS: The declining in the outgrowth of dendrites was observed in neural morphology in a dose dependent manner. The ID50 (Inhibition of neuronal differentiation) of groups 1 and 2 were 130 and 400 &amp;micro;M, respectively.&amp;nbsp; By using RT-PCR, in comparison with MAP2, no significant change was observed in the nestin expression. &amp;nbsp;CONCLUSIONS: Our data about neuronal toxicity were consistent with in vivo and in vitro studies. Therefore, we concluded that ESCs can be used as an efficient model to assess the toxicity of drugs. KEYWORDS: Methamphetamine, Embryonic stem cell, Neural differentiation, Toxicity</Abstract></Article></ArticleSet>
