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溴隐亭,一种多巴胺激动剂,可直接抑制大鼠睾丸间质细胞的睾酮生成。

Bromocriptine, a dopamine agonist, directly inhibits testosterone production by rat Leydig cells.

作者信息

Chambon M, Grizard G, Boucher D

出版信息

Andrologia. 1985 Mar-Apr;17(2):172-7. doi: 10.1111/j.1439-0272.1985.tb00981.x.

Abstract

We investigated the direct effects of bromocriptine (BR) on both basal and hCG-stimulated testosterone production by rat collagenase-dispersed Leydig cells. In a final volume of 2.2 ml, 2.10(6) Leydig cells were incubated at 33 degrees C for 3 h either alone or with various amounts of hCG (1. 10. 10(2). 10(3). 10(4) mUI/vial) and BR (1.5 10(-9), 1.5 10(-7), 1.5 10(-5) M); BR was dissolved in 20 microliters of ethanol. BR (1.5 10(-5) M) decreased significantly both basal and hCG-stimulated testosterone production whereas at lower doses, BR had no effect. These results suggest that the dopamine itself may regulate rat Leydig cell function and that there is room for criticism of BR-induced hypoprolactinemia as an experimental model to study the effect of prolactin on the androgenic function.

摘要

我们研究了溴隐亭(BR)对大鼠胶原酶分散的睾丸间质细胞基础状态以及人绒毛膜促性腺激素(hCG)刺激下睾酮生成的直接影响。在最终体积为2.2毫升的培养液中,将2×10⁶个睾丸间质细胞于33℃孵育3小时,细胞单独培养或与不同量的hCG(1、10、10²、10³、10⁴ mUI/瓶)以及BR(1.5×10⁻⁹、1.5×10⁻⁷、1.5×10⁻⁵ M)共同培养;BR溶解于20微升乙醇中。BR(1.5×10⁻⁵ M)显著降低了基础状态以及hCG刺激下的睾酮生成,而在较低剂量时,BR没有作用。这些结果表明多巴胺自身可能调节大鼠睾丸间质细胞功能,并且作为研究催乳素对雄激素功能影响的实验模型,对BR诱导的低催乳素血症存在质疑的空间。

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