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过氧化氢阻断激素敏感型胆固醇转运至大鼠黄体细胞线粒体的证据。

Evidence that hydrogen peroxide blocks hormone-sensitive cholesterol transport into mitochondria of rat luteal cells.

作者信息

Behrman H R, Aten R F

机构信息

Department of Obstetrics and Gynecology, Yale University School of Medicine, New Haven, Connecticut 06510.

出版信息

Endocrinology. 1991 Jun;128(6):2958-66. doi: 10.1210/endo-128-6-2958.

Abstract

In luteal and granulosa cells, hydrogen peroxide abruptly inhibits activation of adenylate cyclase by receptor-bound gonadotropin and blocks steroidogenesis. In the present studies a post-cAMP site of peroxide action on inhibition of steroidogenesis was investigated. Steroidogenesis, stimulated by dibutyryl or 8-bromo-cAMP, was inhibited by hydrogen peroxide. Yet, cAMP-dependent protein kinase activation in cytosol or intact cells was unaffected by peroxide treatment. Hydrogen peroxide also did not inhibit the activity of cholesterol esterase and acyl coenzyme-A:acyltransferase. Progesterone synthesis was maximally increased 5- to 50-fold with 25- and 22-hydroxycholesterol, respectively. Unlike that seen with cAMP analogs and LH, however, progestin synthesis stimulated by these cell- and mitochondria-permeant cholesterol analogs was not inhibited by hydrogen peroxide. Treatment of animals with amino-glutethimide produces a marked accumulation of steroidogenic cholesterol substrate and a large increase in hormone-independent steroidogenesis in subsequently isolated and washed luteal tissue. In this paradigm, hydrogen peroxide did not inhibit elevated basal progesterone synthesis in luteal cells produced by in vivo aminoglutethimide treatment, yet LH-stimulated steroidogenesis was blocked. However, treatment of luteal cells with hydrogen peroxide inhibited pregnenolone synthesis in isolated mitochondria, an effect partially reversed by the addition of luteal cell cytosol. In summary, while peroxide inhibited cAMP-dependent steroidogenesis, it did not appear to inhibit protein kinase activation or mobilization of cholesterol from intracellular esterified stores. Although peroxide inhibited pregnenolone synthesis, it had no effect on steroidogenesis when substrate was made available by either addition of cholesterol analogs or prior treatment with aminoglutethimide in vivo. We conclude, therefore, that hydrogen peroxide inhibits steroidogenesis by blocking intracellular transport of cholesterol to mitochondria or translocation of cholesterol across the outer mitochondrial membrane.

摘要

在黄体细胞和颗粒细胞中,过氧化氢会突然抑制受体结合促性腺激素对腺苷酸环化酶的激活,并阻断类固醇生成。在本研究中,对过氧化氢作用于抑制类固醇生成的环磷酸腺苷(cAMP)后位点进行了研究。由二丁酰cAMP或8-溴-cAMP刺激的类固醇生成受到过氧化氢的抑制。然而,过氧化氢处理对胞质溶胶或完整细胞中cAMP依赖性蛋白激酶的激活没有影响。过氧化氢也不抑制胆固醇酯酶和酰基辅酶A:酰基转移酶的活性。分别用25-羟基胆固醇和22-羟基胆固醇可使孕酮合成最大增加5至50倍。然而,与cAMP类似物和促黄体生成素(LH)不同的是,这些可穿透细胞和线粒体的胆固醇类似物刺激的孕激素合成不受过氧化氢的抑制。用氨鲁米特处理动物会导致类固醇生成胆固醇底物显著积累,并且在随后分离和洗涤的黄体组织中激素非依赖性类固醇生成大幅增加。在这种模式下,过氧化氢不会抑制体内氨鲁米特处理产生的黄体细胞中基础孕酮合成的升高,但LH刺激的类固醇生成会被阻断。然而,用过氧化氢处理黄体细胞会抑制分离线粒体中孕烯醇酮的合成,添加黄体细胞胞质溶胶可部分逆转这一效应。总之,虽然过氧化氢抑制cAMP依赖性类固醇生成,但它似乎不会抑制蛋白激酶激活或从细胞内酯化储存中动员胆固醇。尽管过氧化氢抑制孕烯醇酮合成,但当通过添加胆固醇类似物或体内预先用氨鲁米特处理使底物可用时,它对类固醇生成没有影响。因此,我们得出结论,过氧化氢通过阻断胆固醇向线粒体的细胞内转运或胆固醇跨线粒体外膜的易位来抑制类固醇生成。

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