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他汀类药物在体外显著抑制大鼠睾丸间质细胞的睾酮生成:对男性的影响。

Statin drugs markedly inhibit testosterone production by rat Leydig cells in vitro: implications for men.

作者信息

Klinefelter G R, Laskey J W, Amann R P

机构信息

United States Environmental Protection Agency, Office of Research and Development, National Health and Environmental Effects Research Laboratory, Toxicology Assessment Division, Reproductive Toxicology Facility, Durham, NC 27713, United States.

United States Environmental Protection Agency, Office of Research and Development, National Health and Environmental Effects Research Laboratory, Toxicology Assessment Division, Reproductive Toxicology Facility, Durham, NC 27713, United States.

出版信息

Reprod Toxicol. 2014 Jun;45:52-8. doi: 10.1016/j.reprotox.2013.12.010. Epub 2014 Jan 22.

Abstract

Statin drugs lower blood cholesterol by inhibiting hepatic 3-hydroxy-3-methylglutaryl-Coenzyme-A reductase. Statins are known to inhibit sterol production in the testis, but effect of statins on testosterone production has not been studied critically in vitro and clinical data are controversial. We measured 18-h testosterone production in vitro, using highly purified rat Leydig cells exposed to atorvastatin, mevastatin, or simvastatin and also determined if statin-induced inhibition of testosterone production could be bypassed with substrate distal to cholesterol. Statins had no effect on testosterone production during culture without LH. However, with 10ng/mL LH, testosterone production was ≥12-fold higher and markedly inhibited (-40%) by ≥0.3μM statin. Leydig cells provided sub-saturating pregnenolone or progesterone to bypass the site of statin action, maintained LH-stimulated testosterone production at or above amounts observed with LH stimulation and no statin. Pregnenolone resulted in greater testosterone production, but LH responsiveness was lost. With progesterone, LH responsiveness was maintained.

摘要

他汀类药物通过抑制肝脏3-羟基-3-甲基戊二酰辅酶A还原酶来降低血液胆固醇水平。已知他汀类药物会抑制睾丸中的固醇生成,但他汀类药物对睾酮生成的影响尚未在体外进行严格研究,临床数据也存在争议。我们使用高度纯化的大鼠睾丸间质细胞,在体外测量了18小时的睾酮生成情况,这些细胞暴露于阿托伐他汀、美伐他汀或辛伐他汀中,并且还确定了是否可以用胆固醇远端的底物绕过他汀类药物诱导的睾酮生成抑制作用。在没有促黄体生成素(LH)的培养过程中,他汀类药物对睾酮生成没有影响。然而,在存在10ng/mL LH的情况下,睾酮生成量≥12倍增加,并且≥0.3μM的他汀类药物会使其显著抑制(-40%)。睾丸间质细胞提供亚饱和量的孕烯醇酮或孕酮以绕过他汀类药物的作用位点,维持LH刺激的睾酮生成量处于或高于LH刺激且无他汀类药物时所观察到的量。孕烯醇酮导致更高的睾酮生成量,但失去了对LH的反应性。使用孕酮时,对LH的反应性得以维持。

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