首页> 外文期刊>Journal of Environmental Science and Health. Part B, Pesticides, Food Contaminants and Agricultural Wastes >Chlorpyrifos-induced toxicity has no gender selectivity in the early fetal brain
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Chlorpyrifos-induced toxicity has no gender selectivity in the early fetal brain

机译:紫外线诱导的毒性在早期胎儿脑中没有性别选择性

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摘要

Organophosphorus pesticides induce gender-specific developmental neurotoxicity after birth, especially in adolescents and adults. However, whether and when the selectivity occurs in fetus remains unclear. In this study, we analyzed chlorpyrifos (CPF)-induced neurotoxicity in the early fetal brains of male and female mice. The gestational dams were administered 0, 1, 3, and 5 mg/(kg.d) CPF during gestational days (GD)7-11, and brains from the fetuses were isolated and analyzed on GD12. Fetal gender was identified by PCR technique based on male-specificSrygene andMyogcontrol gene. The body weight and head weight, the activity of acetylcholinesterase (AChE), superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPX), and the content of malondialdehyde (MDA), as well as the oxidative stress-related gene expression were examined. Our results showed that CPF pretreatment induced AChE inhibition in GD12 fetal brain. CPF treatment activated SOD and GPX but not CAT and MDA. For oxidative stress-related gene expression, CPF pretreatment increased mRNA expression ofSod1,Cat,Gpx1, andGpx2in the fetal brain on GD12. The statistical analysis did not show gender-selective CPF-induced toxicity. Moreover, our results showed that although the gestational exposure to CPF could elicit abnormalities in the early fetal brain, the toxicity observed was not gender-specific.
机译:有机磷杀虫剂在出生后诱导性别特异性发育神经毒性,特别是在青少年和成年人。然而,无论是在胎儿中发生选择性仍然不清楚。在这项研究中,我们分析了氯吡啶(CPF) - 在雄性和雌性小鼠的早期胎儿大脑中引起的神经毒性。在妊娠期(GD)7-11期间施用妊娠局部施用0,1,3和5mg /(kg.d)CPF,并分析来自胎儿的大脑并在GD12上分析。基于雄性细胞晶体基因的PCR技术鉴定了胎儿性别。体重和头部重量,乙酰胆碱酯酶(疼痛),超氧化物歧化酶(SOD),过氧化氢酶(谷胱甘肽过氧化物酶(GPX)和丙二醛(MDA)的含量,以及氧化应激相关基因检查表达。我们的研究结果表明,CPF预处理诱导GD12胎儿脑中的疼痛抑制。 CPF治疗激活SOD和GPX,但不是CAT和MDA。对于氧化应激相关的基因表达,CPF预处理增加了MRNA表达,患有GD12的胎儿脑的mRNA表达。统计分析没有显示出性别选择性的CPF诱导的毒性。此外,我们的结果表明,尽管妊娠期CPF暴露可能引起早期胎儿的异常,但观察到的毒性不是性别特异性。

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