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超氧自由基对大鼠黄体孕酮分泌的细胞内调节

Intracellular regulation of progesterone secretion by the superoxide radical in the rat corpus luteum.

作者信息

Sawada M, Carlson J C

机构信息

Biology Department, University of Waterloo, Ontario, Canada.

出版信息

Endocrinology. 1996 May;137(5):1580-4. doi: 10.1210/endo.137.5.8612488.

Abstract

In this study we examined the prospect that the superoxide radical (SOR) is involved in the mechanism by which LH stimulates progesterone secretion in the rat corpus luteum (CL). Treatment of dispersed CL cells with low doses of LH or a SOR-generating system (xanthine-xanthine oxidase) resulted in a significant increase in progesterone release and SOR production. High doses of each treatment were inhibitory. SOR generation also decreased hCG binding. To determine whether SOR may be required for progesterone secretion, dispersed cells were electroporated with antioxidant enzymes [superoxide dismutase (SOD) and catalase (CAT)] and treated with either low (50 ng) stimulatory or high (20 micrograms) inhibitory doses of LH. At 50 ng LH, insertion of SOD or CAT dose-dependently inhibited progesterone secretion. However, at high doses of LH (20 micrograms), which are associated with high levels of SOR, electroporation of SOD or CAT produced the opposite response. This stimulatory response of SOD or CAT on progesterone release was also dose related. These results indicate that SOR may be involved in the mechanisms that stimulate as well as those that inhibit progesterone release. The effect on progesterone secretion appears to be dose related, with small increases associated with stimulation and high levels involved in inhibition of secretion.

摘要

在本研究中,我们探讨了超氧阴离子自由基(SOR)是否参与促黄体生成素(LH)刺激大鼠黄体(CL)分泌孕酮的机制。用低剂量的LH或一个SOR生成系统(黄嘌呤-黄嘌呤氧化酶)处理分散的CL细胞,导致孕酮释放和SOR产生显著增加。每种处理的高剂量则具有抑制作用。SOR的生成也降低了人绒毛膜促性腺激素(hCG)的结合。为了确定孕酮分泌是否需要SOR,用抗氧化酶[超氧化物歧化酶(SOD)和过氧化氢酶(CAT)]对分散的细胞进行电穿孔,并分别用低剂量(50 ng)的刺激性LH或高剂量(20 μg)的抑制性LH进行处理。在50 ng LH处理时,导入SOD或CAT会剂量依赖性地抑制孕酮分泌。然而,在与高水平SOR相关的高剂量LH(20 μg)处理时,导入SOD或CAT产生了相反的反应。SOD或CAT对孕酮释放的这种刺激反应也与剂量相关。这些结果表明,SOR可能参与刺激以及抑制孕酮释放的机制。对孕酮分泌的影响似乎与剂量相关,少量增加与刺激有关,而高水平则参与抑制分泌。

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