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花生四烯酸作为大鼠卵巢中促黄体生成素释放激素作用的刺激介质。

Arachidonic acid as a stimulatory mediator of luteinizing hormone-releasing hormone action in the rat ovary.

作者信息

Wang J, Leung P C

机构信息

Department of Obstetrics and Gynecology, University of British Columbia, Grace Hospital, Vancouver, Canada.

出版信息

Endocrinology. 1989 Apr;124(4):1973-9. doi: 10.1210/endo-124-4-1973.

Abstract

The present study further examined the role of arachidonic acid (AA) in the action of LHRH on ovarian steroidogenesis. Rat granulosa cells were incubated with LHRH and/or AA in the presence of FSH for 24 h. As expected, the presence of LHRH markedly attenuated the FSH-induced progesterone (P) production. AA by itself did not affect the magnitude of P production induced by FSH. However, when AA (10(-5) M) was added during the last 6 h to the cultures containing LHRH and FSH, AA partially reversed the inhibitory action of LHRH (by 42%). Likewise, addition of AA partially antagonized the inhibitory effect of 12-O-tetradecanoylphorbol-13-acetate (TPA; 10(-9) M) on FSH-induced P production (by 71%). Pretreatment of granulosa cells with TPA or LHRH without FSH for 18 h did not alter the stimulatory effect of AA on P formation during the subsequent 6-h culture period. In other experiments granulosa cells were incubated for 5 h in the absence of FSH. Treatment with AA, TPA, or LHRH alone caused significant increase in P production. Combined treatment with AA and LHRH or AA plus TPA showed additive effects on P formation. By contrast, AA failed to potentiate the effect of LHRH or TPA on 20 alpha-hydroxyprogesterone accumulation. Although AA by itself slightly stimulated 20 alpha-hydroxyprogesterone production, the magnitude was much less than that induced by TPA or LHRH. When 25-hydroxycholesterol was present in the incubation medium, P production was significantly increased. In the presence of 25-hydroxycholesterol, AA further increased P formation, but did not enhance the stimulatory actions of LHRH or TPA in this regard. Taken together, these results further support the hypothesis that AA (or its metabolites) play a stimulatory role in the direct action of LHRH on ovarian steroidogenesis.

摘要

本研究进一步探讨了花生四烯酸(AA)在促性腺激素释放激素(LHRH)对卵巢甾体激素生成作用中的角色。将大鼠颗粒细胞在促卵泡激素(FSH)存在的情况下与LHRH和/或AA一起孵育24小时。正如预期的那样,LHRH的存在显著减弱了FSH诱导的孕酮(P)生成。AA本身并不影响FSH诱导的P生成量。然而,当在最后6小时向含有LHRH和FSH的培养物中加入AA(10⁻⁵ M)时,AA部分逆转了LHRH的抑制作用(逆转了42%)。同样,加入AA部分拮抗了12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯(TPA;10⁻⁹ M)对FSH诱导的P生成的抑制作用(拮抗了71%)。在没有FSH的情况下,用TPA或LHRH预处理颗粒细胞18小时,并不改变随后6小时培养期内AA对P形成的刺激作用。在其他实验中,颗粒细胞在没有FSH的情况下孵育5小时。单独用AA、TPA或LHRH处理导致P生成显著增加。AA与LHRH联合处理或AA加TPA联合处理对P形成显示出相加作用。相比之下,AA未能增强LHRH或TPA对20α - 羟孕酮积累的作用。尽管AA本身轻微刺激了20α - 羟孕酮的生成,但其幅度远小于TPA或LHRH诱导的幅度。当孵育培养基中存在25 - 羟胆固醇时,P生成显著增加。在存在25 - 羟胆固醇的情况下,AA进一步增加了P的形成,但在这方面并未增强LHRH或TPA的刺激作用。综上所述,这些结果进一步支持了以下假说:AA(或其代谢产物)在LHRH对卵巢甾体激素生成的直接作用中起刺激作用。

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