大鼠肝脏、睾丸、肾脏和乳腺中催乳素受体的短期体内调节。

Receptor Pub Date : 1992-01-01
I Barash, Z Madar, A Gertler
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引用次数: 0

摘要

17- β -雌二醇输注3 h后,雄性大鼠微粒体肝脏部分PRL受体(PRL)数量增加100%以上,但不影响激素受体亲和力。PRL受体在睾丸中也有少量但显著的增加,而在肾脏中没有。在同样的时间内,雌性雌性大鼠的睾丸激素输注导致肝脏PRL受体的一些不显著下降,但乳腺和肾脏的PRL受体没有明显下降。雄性输注睾酮或雌性输注17- β -雌二醇不会改变PRL和生长激素受体的数量或亲和力。两种激素均未影响血清PRL水平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Short-term in vivo regulation of prolactin receptors in the liver, testes, kidneys, and mammary gland of rats.

Infusion of 17-beta-estradiol for 3 h caused a more than 100% increase in the number of PRL receptors (PRL) in the microsomal liver fraction of male rats without affecting the hormone-receptor affinity. A small but significant increase in PRL receptors also was found in testes but not kidneys. Testosterone infusion to female virgin rats for a similar time period resulted in some nonsignificant decreases in PRL receptors in the liver but not the mammary gland or kidneys. Testosterone infusion to males or 17-beta-estradiol infusion to females did not change the number or affinity of PRL and growth hormone receptors. The level of serum PRL was not influenced during infusion with both hormones.

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