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一氧化氮:亚洲鲶鱼(胡子鲶)睾丸间质细胞类固醇生成的自分泌调节因子。

Nitric oxide: An autocrine regulator of Leydig cell steroidogenesis in the Asian catfish, Clarias batrachus.

作者信息

nee Pathak Neelima Dubey, Lal Bechan

机构信息

Fish Endocrinology Laboratory, Department of Zoology, Banaras Hindu University, Varanasi 221 005, UP, India.

出版信息

Gen Comp Endocrinol. 2008 Sep 1;158(2):161-7. doi: 10.1016/j.ygcen.2008.06.009. Epub 2008 Jul 10.

Abstract

Nitric oxide has been recognized as an important inter- and intra-cellular modulator of testicular steroidogenesis in higher vertebrates with conflicting results. Moreover, its role in regulation of testicular steroidogenesis in ectothermic vertebrates is non-existent. The present study was, therefore, undertaken to examine whether Leydig cells of a freshwater catfish, Clarias batrachus produce nitric oxide (NO), if so, does it regulate its steroidogenic activity? The purified Leydig cells were stained histochemically for NADPH-diaphorase (NADPH-d) activity, and immunocytochemically for neuronal and inducible nitric oxide synthase (nNOS and iNOS) like molecules. Leydig cells were also incubated with NOS inhibitor, N-nitro-l-arginine methyl ester (l-NAME), and NO donor, sodium nitroprusside (SNP). NO and testosterone released in incubation medium were analyzed. A distinct positive NAPDH-d staining was observed in Leydig cells. These cells also exhibited immunoprecipitation of variable intensity with nNOS and iNOS antibodies. Further, l-NAME treatment caused significant suppression in NO production and elevation in testosterone secretion by Leydig cells. On the contrary, exposure of Leydig cells to SNP resulted in increased NO production with concomitant decline in testosterone level. Thus, the present study reports NO production by Leydig cells in fish for the first time, which appears to inhibit its own androgen production.

摘要

一氧化氮已被公认为高等脊椎动物睾丸类固醇生成过程中一种重要的细胞间和细胞内调节剂,但其结果存在争议。此外,它在变温脊椎动物睾丸类固醇生成调节中的作用尚不存在。因此,本研究旨在探讨淡水鲶鱼(胡子鲶)的睾丸间质细胞是否产生一氧化氮(NO),如果产生,它是否调节其类固醇生成活性?对纯化的睾丸间质细胞进行组织化学染色以检测NADPH-黄递酶(NADPH-d)活性,并进行免疫细胞化学染色以检测神经元型和诱导型一氧化氮合酶(nNOS和iNOS)样分子。睾丸间质细胞还与一氧化氮合酶抑制剂N-硝基-L-精氨酸甲酯(L-NAME)和一氧化氮供体硝普钠(SNP)一起孵育。分析孵育培养基中释放的一氧化氮和睾酮。在睾丸间质细胞中观察到明显的阳性NADPH-d染色。这些细胞还对nNOS和iNOS抗体表现出不同强度的免疫沉淀。此外,L-NAME处理导致睾丸间质细胞一氧化氮产生显著抑制,睾酮分泌升高。相反,睾丸间质细胞暴露于SNP导致一氧化氮产生增加,同时睾酮水平下降。因此,本研究首次报道了鱼类睾丸间质细胞产生一氧化氮,这似乎抑制了其自身雄激素的产生。

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