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心房利钠因子在体外可刺激小鼠睾丸间质细胞产生睾酮。

Testosterone production by mouse Leydig cells is stimulated in vitro by atrial natriuretic factor.

作者信息

Mukhopadhyay A K, Bohnet H G, Leidenberger F A

出版信息

FEBS Lett. 1986 Jun 23;202(1):111-6. doi: 10.1016/0014-5793(86)80659-7.

Abstract

The synthetic atrial peptides, rat atrial natriuretic peptide, atriopeptin I and atriopeptin II, stimulated testosterone production by mouse Leydig cells in a time- and concentration-dependent manner. The maximum stimulation of the steroidogenesis in response to the peptides was 6-10-fold over the basal level, as compared with 20-24-fold stimulation obtained with saturating concentrations of hCG. The stimulation of steroidogenesis by the most potent peptide, atriopeptin II, was markedly enhanced in the presence of the phosphodiesterase inhibitor, 3-isobutyl-1-methylxanthine, suggesting an involvement of cyclic nucleotides. However, neither basal nor hCG-stimulated levels of cAMP were altered by the peptide, though testosterone production in response to submaximal concentrations of hCG was increased in the presence of atriopeptin II. The nature of the second messenger involved and the mechanism of action of the atrial peptides may be elucidated by further research in progress.

摘要

合成心房肽、大鼠心房利钠肽、心房肽I和心房肽II以时间和浓度依赖性方式刺激小鼠睾丸间质细胞产生睾酮。与用饱和浓度的人绒毛膜促性腺激素(hCG)获得的20 - 24倍刺激相比,这些肽对类固醇生成的最大刺激是基础水平的6 - 10倍。在磷酸二酯酶抑制剂3 - 异丁基 - 1 - 甲基黄嘌呤存在下,最有效的肽心房肽II对类固醇生成的刺激显著增强,提示环核苷酸参与其中。然而,该肽既未改变基础cAMP水平,也未改变hCG刺激的cAMP水平,尽管在心房肽II存在下,对亚最大浓度hCG的睾酮生成增加。正在进行的进一步研究可能会阐明所涉及的第二信使的性质以及心房肽的作用机制。

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