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杀菌剂N-(3,5-二氯苯基)琥珀酰亚胺在体内和体外试验中的抗雄激素活性。

The antiandrogenic activity of the fungicide N-(3, 5-dichlorophenyl) succinimide in in vivo and in vitro assays.

作者信息

Zhang Jun, Zhang GuoJun, Zheng YiFan, Zhu HuiJuan, Yang Jun, Yao GengDong, Zhu XinQiang

机构信息

Department of Toxicology, School of Medicine, Zhejiang University, P. R. China.

出版信息

J Reprod Dev. 2007 Jun;53(3):535-43. doi: 10.1262/jrd.18131. Epub 2007 Feb 19.

Abstract

Antiandrogens can cause reproductive disorders in humans and wild animals. In the present study, we tested whether the fungicide N-(3, 5-dichlorophenyl) succinimide (NDPS) acts as an antiandrogen using in vitro and in vivo assays. A transient transfection system based on luciferase activity was utilized for in vitro analysis of the antiandrogeic activity of NDPS. Hershberger assay was used to analyze the antiandrogenic activity of NDPS in rats. The expressions of the androgen-responsive genes testosterone-repressed prostatic message-2 (TRPM-2) and prostate specific binding protein polypeptide C3 (PBP C3) in the rat ventral prostate were measured using real-time PCR. Our results indicated that NDPS can block 5-dehydrotestosterone (DHT)-induced androgen receptor (AR) activity in transiently transfected HepG2 cells (-5 log M). In the Hershberger assay, the weights of the seminal vesicles and levator ani/bulbocavernosus muscles were significantly decreased (P<0.05) in all NDPS groups, and the weights of the ventral prostate, dorsolateral prostate, and Cowper's glands were significantly decreased (P<0.05) in the 100 and 200 mg/kg NDPS groups. NDPS only decreased (P<0.05) the expression of PBP C3 and had no effect on the level of TRPM-2 (P>0.05). In conclusion, NDPS is a moderate antiandrogen that elicits antiandrogenic effects at least partly by antagonizing AR and increasing the expression of PBP C3.

摘要

抗雄激素药物可导致人类和野生动物出现生殖紊乱。在本研究中,我们通过体外和体内试验检测了杀菌剂N-(3,5-二氯苯基)琥珀酰亚胺(NDPS)是否具有抗雄激素作用。利用基于荧光素酶活性的瞬时转染系统对NDPS的抗雄激素活性进行体外分析。采用赫什伯格试验分析NDPS对大鼠的抗雄激素活性。使用实时PCR检测大鼠腹侧前列腺中雄激素反应基因睾酮抑制前列腺信使-2(TRPM-2)和前列腺特异性结合蛋白多肽C3(PBP C3)的表达。我们的结果表明,NDPS可在瞬时转染的HepG2细胞中阻断5-脱氢睾酮(DHT)诱导的雄激素受体(AR)活性(-5 log M)。在赫什伯格试验中,所有NDPS组的精囊和提肛肌/球海绵体肌重量均显著降低(P<0.05),100和200 mg/kg NDPS组的腹侧前列腺、背外侧前列腺和考珀氏腺重量显著降低(P<0.05)。NDPS仅降低(P<0.05)PBP C3的表达,对TRPM-2水平无影响(P>0.05)。总之,NDPS是一种中度抗雄激素药物,其抗雄激素作用至少部分是通过拮抗AR和增加PBP C3的表达来实现的。

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