Tsai Shiow-Chwen, Lu Chien-Chen, Lin Chiu-Shuang, Wang Paulus S
Central Laboratory, Shin Kong Wu Ho-Su Memorial Hospital, Taipei, Taiwan, Republic of China.
J Cell Biochem. 2003 Dec 15;90(6):1276-86. doi: 10.1002/jcb.10738.
It has been well known that reactive oxygen species (ROS) are produced in the steroidogenic pathway and spermatozoa. H2O2, one of ROS produced by spermatozoa, appears to be a primary toxic agent. In the present study, we examined the effects of H2O2 on the basal and evoked-testosterone release from primary Leydig cells, the protein expressions of cytochrome P450 side chain cleavage enzyme (P450scc) and steroidogenic acute regulatory (StAR) protein were also investigated. Our preparation was found to contain approximately 87% Leydig cells and very few macrophages. The results demonstrated that H2O2 (>1 x 10(-4) M) significantly inhibited the basal and hCG-stimulated testosterone release. H2O2 abolished forskolin- or 8-Br-cAMP-evoked testosterone release. In the presence of pregnenolone, progesterone, or androstenedione, the inhibitory effect of H2O2 on testosterone release was prevented. H2O2 also inhibited pregnenolone production in the presence of trilostane (an inhibitor of 3beta-hydroxysteroid dehydrogenase), therefore diminished the activity of P450scc in Leydig cells. In addition to the inhibition of hormone secretion, H2O2 also regulated steroidogenesis by diminishing protein expression of StAR. These results suggest that H2O2 acts directly on rat Leydig cells to diminish testosterone production by inhibiting P450scc activity and StAR protein expression.
众所周知,活性氧(ROS)在类固醇生成途径和精子中产生。过氧化氢(H2O2)是精子产生的ROS之一,似乎是主要的毒性因子。在本研究中,我们检测了H2O2对原代睾丸间质细胞基础和刺激后睾酮释放的影响,还研究了细胞色素P450侧链裂解酶(P450scc)和类固醇生成急性调节蛋白(StAR)的蛋白表达。我们发现制备物中约含87%的睾丸间质细胞,巨噬细胞很少。结果表明,H2O2(>1×10^(-4) M)显著抑制基础和人绒毛膜促性腺激素(hCG)刺激的睾酮释放。H2O2消除了福司可林或8-溴环磷腺苷(8-Br-cAMP)刺激的睾酮释放。在孕烯醇酮、孕酮或雄烯二酮存在的情况下,H2O2对睾酮释放的抑制作用被阻止。在曲洛司坦(一种3β-羟基类固醇脱氢酶抑制剂)存在的情况下,H2O2也抑制孕烯醇酮的产生,因此降低了睾丸间质细胞中P450scc的活性。除了抑制激素分泌外,H2O2还通过减少StAR的蛋白表达来调节类固醇生成。这些结果表明,H2O2直接作用于大鼠睾丸间质细胞,通过抑制P450scc活性和StAR蛋白表达来减少睾酮的产生。