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Antisteroidogenic effects of hydrogen peroxide on rat granulosa cells

机译:过氧化氢对大鼠颗粒细胞的抗类固醇作用

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Rat granulosa cells (GCs) were treated with human chorionic gonadotropin (hCG), 8-bromo-adenosine 3′,5′-cyclic monophosphate (8-Br-cAMP), forskolin, phorbol 12-myristate 13-acetate (PMA), A23187 or pregnenolone in the absence or presence of hydrogen peroxide (H 2O 2). Different doses of trilostane were applied to GCs treated with steroidogenic precursors, that is, 25-hydroxy-cholesterol (25-OH-C) in the absence or presence of H 2O 2. Results showed that all of the chemicals stimulated the progesterone (PG) release from rat GCs, but the stimulatory effects were inhibited by H 2O 2 dose-dependently. 25-OH-C stimulated the PG release, which was inhibited by H 2O 2 in the presence of trilostane. H 2O 2 attenuated steroidogenic acute regulatory (StAR) protein expression, but did not alter the expression of cytochrome P450 side chain cleavage (P450scc) in Western blotting. This study indicated that H 2O 2 inhibited PG production by GCs via cAMP pathway, protein kinase C (PKC) and the activities of intracellular calcium, P450scc and StAR protein.
机译:用人绒毛膜促性腺激素(hCG),8-溴腺苷3',5'-环一磷酸(8-Br-cAMP),毛喉素,佛波醇12-肉豆蔻酸酯13-乙酸酯(PMA)处理大鼠颗粒细胞(GCs), A23187或孕烯醇酮在不存在或存在过氧化氢(H 2O 2)的情况下。在没有或没有H 2O 2的情况下,将不同剂量的Trilostane应用于用类固醇生成前体(即25-羟基胆固醇(25-OH-C))处理的GC。结果表明,所有化学物质均刺激了孕酮(PG) )从大鼠GC中释放,但H 2O 2剂量依赖性抑制其刺激作用。 25-OH-C刺激了PG的释放,在三氯杀螨醇存在下H 2O 2抑制了PG的释放。 H 2O 2减弱了类固醇生成的急性调节(StAR)蛋白的表达,但在Western blotting中并未改变细胞色素P450侧链裂解(P450scc)的表达。这项研究表明,H 2O 2通过cAMP途径,蛋白激酶C(PKC)和细胞内钙,P450scc和StAR蛋白的活性抑制了GC产生的PG。

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