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经过葵莫司特处理后,雌性蒙古沙鼠(Meriones unguiculatus)的生殖器官、类固醇激素和 CYP450 酶的反应随时间的变化。

Responses in reproductive organs, steroid hormones and CYP450 enzymes in female Mongolian gerbil (Meriones unguiculatus) over time after quinestrol treatment.

机构信息

Guangdong Key Laboratory of Animal Conservation and Resource Utilization, Guangdong Public Laboratory of Wild Animal Conservation and Utilization, Guangdong Institute of Applied Biological Resources, 510260 Guangzhou, China.

College of Life Science, Hainan Normal University, 571158 Haikou, China; State Key Laboratory of Integrated Management of Pest Insect and Rodents, Institute of Zoology, Chinese Academy of Sciences, 100101 Beijing, China.

出版信息

Pestic Biochem Physiol. 2017 Nov;143:122-126. doi: 10.1016/j.pestbp.2017.08.008. Epub 2017 Aug 5.

Abstract

The aim of this study was to assess the effects and reversibility of the synthetic estrogen compound, quinestrol, on the reproductive organs, steroid hormones, and drug-metabolizing enzymes CYP3A4 and CYP1A2 in liver and kidney over time after two quinestrol treatments in female Mongolian gerbils (Meriones unguiculatus). Female gerbils were treated with 4mg/kg quinestrol (9 gerbils/group, 3 treated group) (1 control group, 0mg/kg) for 3days and treated again after 25days. Animals were killed for collection of samples at 5, 10 and 15days after the second treatment ending. Two interval quinestrol treatments significantly increased uterine weight, with trend of increase over time, but no change could be detected in ovarian weights. Quinestrol treatment increased progesterone and estradiol levels, both with trend of decline over time. Quinestrol increased liver and kidney weights and total enzyme content of CYP3A4 and CYP1A2, with trend of decline over time. On the basis of reversible changes of detoxification enzymes or organs, interval quinestrol treatment effectively and reversibly influenced the reproductive hormone and organ to some extent.

摘要

本研究旨在评估合成雌激素化合物己烯雌酚对雌性蒙古沙鼠(Meriones unguiculatus)生殖器官、甾体激素以及肝、肾中细胞色素 P4503A4(CYP3A4)和细胞色素 P4501A2(CYP1A2)等药物代谢酶的影响和可逆性。雌性沙鼠经 4mg/kg 己烯雌酚(每组 9 只,处理组 3 只)(1 组对照,0mg/kg)处理 3 天,25 天后再次处理。第二次处理结束后 5、10 和 15 天处死动物采集样本。两次间隔己烯雌酚处理显著增加了子宫重量,且随时间呈增加趋势,但卵巢重量无变化。己烯雌酚处理增加了孕酮和雌二醇水平,且随时间呈下降趋势。己烯雌酚增加了肝、肾重量和 CYP3A4 和 CYP1A2 的总酶含量,且随时间呈下降趋势。基于解毒酶或器官的可逆变化,间隔己烯雌酚处理在一定程度上有效且可逆地影响了生殖激素和器官。

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