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抑制素在大鼠腹侧前列腺中的结合特性

Binding characteristics of inhibin in rat ventral prostate.

作者信息

Vanage G R, Phadke M A, Sheth A R

出版信息

Prostate. 1985;6(2):195-203. doi: 10.1002/pros.2990060210.

Abstract

Homogeneous preparation of human seminal plasma inhibin (molecular weight 13,500) was iodinated with 125I to a specific activity of about 40-45 microCi/micrograms and tested for binding to a rat prostate crude membrane preparation. The binding of inhibin was a saturable process as well as time and temperature dependent. This binding was displaceable in a dose-dependent manner by unlabelled inhibin. Other hormones such as LH, FSH, Prl, and TSH from rat or human origin did not influence the binding of labelled inhibin to rat prostate membrane. Of various age groups of rats studied, the maximum binding was observed in 75-day-old rats. The radiolabelled inhibin also showed specific binding to rat pituitary. The preliminary studies regarding involvement of steroids in the control of inhibin receptors in prostate and pituitary indicated that testosterone activates the inhibin receptors at the prostatic level whereas estradiol did not have any effect. However, estradiol increases the pituitary receptors for inhibin as compared to testosterone.

摘要

用人精浆抑制素(分子量13,500)的均一制剂与125I进行碘化,使其比活约为40 - 45微居里/微克,并测试其与大鼠前列腺粗膜制剂的结合情况。抑制素的结合是一个可饱和的过程,且与时间和温度有关。这种结合可被未标记的抑制素以剂量依赖的方式取代。来自大鼠或人类的其他激素,如促黄体生成素(LH)、促卵泡生成素(FSH)、催乳素(Prl)和促甲状腺激素(TSH),并不影响标记的抑制素与大鼠前列腺膜的结合。在所研究的不同年龄组大鼠中,75日龄大鼠的结合量最高。放射性标记的抑制素也显示出与大鼠垂体的特异性结合。关于类固醇参与前列腺和垂体中抑制素受体调控的初步研究表明,睾酮在前列腺水平激活抑制素受体,而雌二醇没有任何作用。然而,与睾酮相比,雌二醇会增加垂体中抑制素的受体。

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