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他莫昔芬抑制睾丸间质细胞类固醇生成:体内和体外研究

Tamoxifen inhibits Leydig cell steroidogenesis: in vivo and in vitro studies.

作者信息

Lin T, Murono E P

出版信息

Metabolism. 1982 Jun;31(6):543-7. doi: 10.1016/0026-0495(82)90092-0.

Abstract

Using isolated interstitial cells from testes of Sprague-Dawley rats, we have shown previously that tamoxifen inhibits LH and 8-bromo-cyclic AMP stimulated testosterone synthesis in a dose-dependent manner. The inhibitory effect of tamoxifen could not be reversed with 17 beta-estradiol. The present studies indicate that tamoxifen directly inhibits testosterone response to gonadotropin stimulation both in immature and mature hypophysectomized rats. When interstitial cells were incubated with pregnenolone (5 x 10(-7) M), testosterone levels in the incubation medium were 27.0 +/- 1.9 ng/10(6) cells. Tamoxifen (10(-5) M) significantly inhibited pregnenolone-induced testosterone formation. Tamoxifen also significantly diminished adenylate cyclase activity whereas the binding of hCG to receptor was not affected. These results indicated that several steps of steroidogenesis are inhibited by tamoxifen.

摘要

利用从斯普拉格-道利大鼠睾丸中分离出的间质细胞,我们先前已表明他莫昔芬以剂量依赖的方式抑制促黄体生成素(LH)和8-溴环磷酸腺苷(8-bromo-cyclic AMP)刺激的睾酮合成。他莫昔芬的抑制作用不能被17β-雌二醇逆转。目前的研究表明,他莫昔芬在未成熟和成熟的垂体切除大鼠中均直接抑制睾酮对促性腺激素刺激的反应。当间质细胞与孕烯醇酮(5×10⁻⁷ M)一起孵育时,孵育培养基中的睾酮水平为27.0±1.9 ng/10⁶个细胞。他莫昔芬(10⁻⁵ M)显著抑制孕烯醇酮诱导的睾酮形成。他莫昔芬还显著降低了腺苷酸环化酶活性,而人绒毛膜促性腺激素(hCG)与受体的结合不受影响。这些结果表明,他莫昔芬抑制了类固醇生成的几个步骤。

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