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Gestational atrazine exposure: effects on male reproductive development and metabolite distribution in the dam, fetus, and neonate.

机译:妊娠at去津暴露:对大坝,胎儿和新生儿中男性生殖发育和代谢产物分布的影响。

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Few studies have investigated the long-term effects of atrazine (ATR) following in utero exposure. We evaluated the effects of gestational exposure of Sprague Dawley dams to ATR (0, 1, 5, 20, or 100mg/kg-d) on the reproductive development of male offspring. We also quantified the distribution of ATR and its chlorinated metabolites in maternal, fetal, and neonatal fluid and tissue samples following gestational and/or lactational exposure. Dose-dependent levels of chlorotriazines, primarily diamino-s-chlorotriazine, were present in most samples analyzed, including fetal tissue. In utero exposure to 1-20mg/kg-d ATR did not alter testosterone production, the timing of puberty, play behavior, or other androgen-dependent endpoints of male offspring. Significant maternal toxicity and postnatal mortality were observed at 100mg/kg-d. We conclude that, although levels of chlorotriazines within the fetus were considerable, gestational exposures of 1-20mg/kg-d do not lead to alterations in the measures of male development examined in this study.
机译:很少有研究调查子宫内暴露后at去津(ATR)的长期影响。我们评估了Sprague Dawley大坝的妊娠暴露于ATR(0、1、5、20或100mg / kg-d)对雄性后代生殖发育的影响。我们还量化了妊娠和/或哺乳期暴露后母体,胎儿和新生儿体液和组织样本中ATR及其含氯代谢产物的分布。在大多数分析的样品中,包括胎儿组织中,都存在剂量依赖性的氯三嗪水平,主要是二氨基-s-氯三嗪。在子宫内暴露于1-20mg / kg-d ATR不会改变睾丸激素的产生,青春期的发生,游戏行为或雄性后代的其他雄激素依赖性终点。以100mg / kg-d观察到明显的母体毒性和产后死亡率。我们得出的结论是,尽管胎儿中的氯三嗪水平相当高,但妊娠暴露量为1-20mg / kg-d并不会导致本研究中检测到的男性发育指标发生变化。

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