Short-term in vivo regulation of prolactin receptors in the liver, testes, kidneys, and mammary gland of rats.

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

Abstract

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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大鼠肝脏、睾丸、肾脏和乳腺中催乳素受体的短期体内调节。
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。
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A modeling study of the alpha-subunit of human high-affinity receptor for immunoglobulin-E. Characterization of growth hormone-induced tyrosine-phosphorylated proteins in mouse cells that express GH receptors. Synthetic peptides derived from the steroid binding domain block modulator and molybdate action toward the rat glucocorticoid receptor. Modulation of angiotensin II receptor (AT2) mRNA levels in R3T3 cells. Growth hormone (GH)-induced tyrosine-phosphorylated proteins in cells that express GH receptors.
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