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佛波酯在体外抑制小鼠睾丸间质细胞受促黄体生成素刺激后的类固醇生成。

Phorbol esters inhibit LH stimulated steroidogenesis by mouse Leydig cells in vitro.

作者信息

Mukhopadhyay A K, Bohnet H G, Leidenberger F A

出版信息

Biochem Biophys Res Commun. 1984 Mar 30;119(3):1062-7. doi: 10.1016/0006-291x(84)90882-9.

Abstract

The effect of phorbol esters on the stimulation of testosterone production in response to LH was studied in mouse Leydig cells incubated in vitro. The tumor promoting phorbol esters, Phorbol-12-myristate-13-acetate and Phorbol-12-13-didecanoate at nanomolar concentrations effectively inhibited testosterone production by Leydig cells in response to stimulation by LH, whereas non-tumor promoting phorbol esters were ineffective. When the cells were stimulated by 8Br-cAMP, instead of LH, the testosterone production was stimulated similarly as in the presence of LH, but phorbol esters were without any effect. This suggests that the tumor promoting phorbol esters may act in the Leydig cells by suppressing the stimulation of cAMP production in response to hormonal activation and/or by interfering with the hormone-receptor interaction.

摘要

在体外培养的小鼠睾丸间质细胞中,研究了佛波酯对促黄体生成素(LH)刺激睾酮产生的影响。具有促肿瘤作用的佛波酯,如佛波醇-12-肉豆蔻酸酯-13-乙酸酯和佛波醇-12,13-二癸酸酯,在纳摩尔浓度下能有效抑制睾丸间质细胞对LH刺激的睾酮产生,而非促肿瘤的佛波酯则无效。当用8-溴环磷酸腺苷(8Br-cAMP)而非LH刺激细胞时,睾酮的产生受到的刺激与存在LH时相似,但佛波酯没有任何作用。这表明具有促肿瘤作用的佛波酯可能通过抑制对激素激活的环磷酸腺苷(cAMP)产生的刺激和/或干扰激素-受体相互作用,在睾丸间质细胞中发挥作用。

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