首页> 美国卫生研究院文献>PLoS Clinical Trials >Reduced Hippocampal Dendritic Spine Density and BDNF Expression following Acute Postnatal Exposure to Di(2-Ethylhexyl) Phthalate in Male Long Evans Rats
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Reduced Hippocampal Dendritic Spine Density and BDNF Expression following Acute Postnatal Exposure to Di(2-Ethylhexyl) Phthalate in Male Long Evans Rats

机译:产后长期暴露于雄性长Evans大鼠的邻苯二甲酸二(2-乙基己基)酯后海马树突状棘密度和BDNF表达降低

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摘要

Early developmental exposure to di(2-ethylhexyl) phthalate (DEHP) has been linked to a variety of neurodevelopmental changes, particularly in rodents. The primary goal of this work was to establish whether acute postnatal exposure to a low dose of DEHP would alter hippocampal dendritic morphology and BDNF and caspase-3 mRNA expression in male and female Long Evans rats. Treatment with DEHP in male rats led to a reduction in spine density on basal and apical dendrites of neurons in the CA3 dorsal hippocampal region compared to vehicle-treated male controls. Dorsal hippocampal BDNF mRNA expression was also down-regulated in male rats exposed to DEHP. No differences in hippocampal spine density or BDNF mRNA expression were observed in female rats treated with DEHP compared to controls. DEHP treatment did not affect hippocampal caspase-3 mRNA expression in male or female rats. These results suggest a gender-specific vulnerability to early developmental DEHP exposure in male rats whereby postnatal DEHP exposure may interfere with normal synaptogenesis and connectivity in the hippocampus. Decreased expression of BDNF mRNA may represent a molecular mechanism underlying the reduction in dendritic spine density observed in hippocampal CA3 neurons. These findings provide initial evidence for a link between developmental exposure to DEHP, reduced levels of BDNF and hippocampal atrophy in male rats.
机译:邻苯二甲酸二(2-乙基己基)酯(DEHP)的早期发育暴露与​​多种神经发育变化有关,尤其是在啮齿动物中。这项工作的主要目的是确定出生后低剂量DEHP的急性暴露是否会改变雄性和雌性Long Evans大鼠的海马树突形态和BDNF和caspase-3 mRNA表达。与媒介物处理的雄性对照相比,在雄性大鼠中用DEHP处理导致CA3背海马区神经元的基底和根尖树突的脊柱密度降低。在暴露于DEHP的雄性大鼠中,背海马BDNF mRNA表达也下调。与对照组相比,在用DEHP处理的雌性大鼠中未观察到海马脊柱密度或BDNF mRNA表达的差异。 DEHP处理不影响雄性或雌性大鼠海马caspase-3 mRNA的表达。这些结果表明,雄性大鼠对早期发育的DEHP暴露有性别特异性的脆弱性,因此出生后的DEHP暴露可能会干扰海马的正常突触发生和连接。 BDNF mRNA表达的降低可能代表了在海马CA3神经元中观察到的树突棘密度降低的分子机制。这些发现为雄性大鼠发育暴露于DEHP,降低BDNF水平和海马萎缩之间的联系提供了初步证据。

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