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三氯生对睾丸间质细胞中促黄体生成素诱导的睾酮生物合成的干扰:可能的作用机制。

Disruption of LH-induced testosterone biosynthesis in testicular Leydig cells by triclosan: probable mechanism of action.

作者信息

Kumar Vikas, Balomajumder Chandrajeet, Roy Partha

机构信息

Molecular Endocrinology Laboratory, Department of Biotechnology, Indian Institute of Technology Roorkee, Roorkee 247667, Uttarakhand, India.

出版信息

Toxicology. 2008 Sep 4;250(2-3):124-31. doi: 10.1016/j.tox.2008.06.012. Epub 2008 Jul 9.

DOI:10.1016/j.tox.2008.06.012
PMID:18655822
Abstract

Triclosan (TCS) is an antimicrobial chemical widely used in different commercial preparations. The present study demonstrated the mechanism of action of TCS-induced anti-androgenicity in rat Leydig cells. Treatment of purified cells with increasing concentrations of TCS (0.001, 0.01, 0.1, 1 and 10 microM) resulted in a significantly decreased activity of adenylyl cyclase enzyme which was followed by a decreased synthesis of cAMP. This decreased cAMP level resulted in the disruption of entire steroidogenic cascade causing a depressed synthesis of testosterone. However, TCS-induced decrease in the production of testosterone returned to normalcy when cells were treated with forskolin (an adenylyl cyclase activator). Transcription followed by translational of four prominent steroidogenic enzyme/proteins, cytochrome P450 side chain cleavage (P450scc), 3beta-hydroxysteroid dehydrogenase (3beta-HSD), 17beta-hydroxysteroid dehydrogenase (17beta-HSD) and steroidogenic acute regulatory (StAR) protein, also decreased in a dose-dependent manner in TCS-treated Leydig cells as determined by RT-PCR, enzyme assay and Western blot. These results suggested that the disruption of the activity of adenylyl cyclase enzyme by TCS in turn leads to the disruption of intermediate steroidogenic cascade causing a depressed testosterone production. The study further confirmed the anti-androgenic activity of TCS in Leydig cells with highest effective concentration at 1 microM.

摘要

三氯生(TCS)是一种广泛应用于不同商业制剂中的抗菌化学物质。本研究揭示了TCS在大鼠睾丸间质细胞中诱导抗雄激素作用的机制。用浓度递增的TCS(0.001、0.01、0.1、1和10微摩尔)处理纯化细胞,导致腺苷酸环化酶活性显著降低,随后cAMP合成减少。cAMP水平的降低导致整个类固醇生成级联反应中断,从而使睾酮合成减少。然而,当用福司可林(一种腺苷酸环化酶激活剂)处理细胞时,TCS诱导的睾酮生成减少恢复正常。通过RT-PCR、酶测定和蛋白质印迹法测定,在TCS处理的睾丸间质细胞中,四种主要的类固醇生成酶/蛋白,即细胞色素P450侧链裂解酶(P450scc)、3β-羟基类固醇脱氢酶(3β-HSD)、17β-羟基类固醇脱氢酶(17β-HSD)和类固醇生成急性调节蛋白(StAR)的转录及翻译也呈剂量依赖性降低。这些结果表明,TCS对腺苷酸环化酶活性的破坏进而导致中间类固醇生成级联反应的破坏,从而使睾酮生成减少。该研究进一步证实了TCS在睾丸间质细胞中的抗雄激素活性,其最高有效浓度为1微摩尔。

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