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环核苷酸对离体格拉夫卵泡中前列腺素E生成的刺激作用。

Stimulation by cyclic nucleotides of prostaglandin E production in isolated graafian follicles.

作者信息

Zor U, Strulovici B, Nimrod A, Lindner H R

出版信息

Prostaglandins. 1977 Nov;14(5):947-59. doi: 10.1016/0090-6980(77)90309-4.

Abstract

Rat Graafian follicles isolated intact responded to 8-Br-cyclic AMP and 8-Br-cyclic GMP with increased prostaglandin E (PGE) production during a 6 h incubation. By contrast, 8-Br-cyclic IMP, 8-Br-5' AMP and 8-Br-5' GMP were inactive in this respect. The effect of 8-Br-cyclic AMP and 8-Br-cyclic GMP was noted only after a lag period of about 4 h. Choleragen, LH, and the phosphodiesterase inhibitor (3-isobutyl-l-methyl-xanthine; IBMX) also stimulated PGE production. Actinomycin D and cycloheximide given simultaneously with 8-Br-cyclic AMP or LH prevented the stimulatory effect of these agents. Concomitant addition of arachidonic acid did not overcome the effect of these inhibitors. Administration of hCG in vivo or incubation with LH in vitro did not elevate endogenous ovarian free arachidonate, while PGE production was enhanced. Dexamethasone prevented this stimulatory effect of hCG. Collectively, the results suggest that stimulation of ovarian PGE production by cyclic nucleotides and LH is dependent on de novo synthesis of one or more components of the PG synthetase system rather than on substrate availability. Cyclic nucleotides may mediate the stimulatory effect of gonadotropins on PGE production.

摘要

完整分离的大鼠格拉夫卵泡在6小时孵育期间对8-溴环磷酸腺苷(8-Br-cyclic AMP)和8-溴环磷酸鸟苷(8-Br-cyclic GMP)有反应,前列腺素E(PGE)生成增加。相比之下,8-溴环肌苷酸(8-Br-cyclic IMP)、8-溴-5'-腺苷酸(8-Br-5' AMP)和8-溴-5'-鸟苷酸(8-Br-5' GMP)在这方面无活性。8-溴环磷酸腺苷和8-溴环磷酸鸟苷的作用仅在约4小时的延迟期后才被观察到。霍乱毒素、促黄体生成素(LH)和磷酸二酯酶抑制剂(3-异丁基-1-甲基黄嘌呤;IBMX)也刺激PGE生成。与8-溴环磷酸腺苷或LH同时给予放线菌素D和环己酰亚胺可阻止这些药物的刺激作用。同时添加花生四烯酸并不能克服这些抑制剂的作用。体内给予人绒毛膜促性腺激素(hCG)或体外与LH孵育均未提高内源性卵巢游离花生四烯酸水平,而PGE生成增加。地塞米松可阻止hCG的这种刺激作用。总体而言,结果表明环核苷酸和LH对卵巢PGE生成的刺激依赖于PG合成酶系统一个或多个组分的从头合成,而非底物可用性。环核苷酸可能介导促性腺激素对PGE生成的刺激作用。

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