Stocco D M, Wells J, Clark B J
Department of Biochemistry and Molecular Biology, Texas Tech University Health Sciences Center, Lubbock 79430.
Endocrinology. 1993 Dec;133(6):2827-32. doi: 10.1210/endo.133.6.8243310.
It has previously been reported that treatment of rat luteal cells and human granulosa luteal cells with hydrogen peroxide (H2O2) results in a significant inhibition of steroid production. The mechanism of inhibition in the former was found to be at the level of cholesterol transport into the mitochondria, whereas in the latter it was found to be a result of inhibition of one or more enzymes in the steroidogenic pathway. In the present study we examined the effects of H2O2 on hormone-stimulated steroid production in another steroidogenic cell type, the Leydig cell. Our results demonstrate that treatment of either LH- or cAMP analog [(Bu)2cAMP]-stimulated MA-10 mouse Leydig tumor cells with H2O2 results in a dose-dependent inhibition of the production of progesterone (the major steroid produced in MA-10 cells). It was also observed that similar concentrations of H2O2 resulted in a significant inhibition of protein synthesis, a finding which could in part be responsible for the observed decrease in steroid production. Furthermore, although H2O2 resulted in a dose-dependent inhibition of (Bu)2cAMP-stimulated pregnenolone production, addition of the hydroxylated intermediate 22R-hydroxycholesterol and inhibitors of further pregnenolone metabolism demonstrated that cholesterol side-chain cleavage complex activity was unaffected by H2O2. Conversely, incubation of H2O2-treated cells in the presence of pregnenolone resulted in a very significant inhibition of progesterone synthesis. These data indicate that H2O2 inhibits steroidogenesis in Leydig tumor cells primarily by inhibiting the activity of the 3 beta-hydroxysteroid dehydrogenase, but that other effects of H2O2 such as inhibition of protein synthesis and the transfer of cholesterol to the cholesterol side-chain cleavage complex may also be involved.
此前有报道称,用过氧化氢(H₂O₂)处理大鼠黄体细胞和人颗粒黄体细胞会显著抑制类固醇生成。研究发现,前者的抑制机制是在胆固醇转运至线粒体的水平,而后者则是类固醇生成途径中一种或多种酶受到抑制的结果。在本研究中,我们检测了H₂O₂对另一种类固醇生成细胞类型——睾丸间质细胞中激素刺激的类固醇生成的影响。我们的结果表明,用H₂O₂处理促黄体生成素(LH)或环磷酸腺苷类似物[(Bu)₂cAMP]刺激的MA - 10小鼠睾丸间质瘤细胞,会导致孕酮(MA - 10细胞中产生的主要类固醇)生成呈剂量依赖性抑制。还观察到,相似浓度的H₂O₂会显著抑制蛋白质合成,这一发现可能部分解释了所观察到的类固醇生成减少的现象。此外,尽管H₂O₂导致(Bu)₂cAMP刺激的孕烯醇酮生成呈剂量依赖性抑制,但添加羟基化中间体22R - 羟基胆固醇以及孕烯醇酮进一步代谢的抑制剂表明,胆固醇侧链裂解复合物的活性不受H₂O₂影响。相反,在孕烯醇酮存在的情况下孵育经H₂O₂处理的细胞,会导致孕酮合成受到非常显著的抑制。这些数据表明,H₂O₂主要通过抑制3β - 羟基类固醇脱氢酶的活性来抑制睾丸间质瘤细胞中的类固醇生成,但H₂O₂的其他作用,如抑制蛋白质合成以及胆固醇向胆固醇侧链裂解复合物的转运,可能也参与其中。