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[雌激素在大鼠肝脏中诱导和调节一种特定雌激素结合蛋白的作用]

[Role of estrogens in the induction and regulation of a specific estrogen-binding protein in the rat liver].

作者信息

Smirnova O V, Vishniakova T G, Smirnov A N, Rozen V B

出版信息

Probl Endokrinol (Mosk). 1985 May-Jun;31(3):65-9.

PMID:4059200
Abstract

A study was made of the role of estrogens (E) in the induction and regulation of the level of specific estrogen binding protein (SEBP) in the rat liver using a differentiated quantitative method of its determination. It was shown that E could not replace androgens (A) in the primary determination of the SEPB level, neither did they prevent its A-dependent induction. Multiple administration of 0.4 microgram of estradiol (E2) caused a significant decrease in the SEPB level in intact and castrated male rats as well as in ovariectomized females with the A-induced SEPB level. Multiple administration of even 10 micrograms of E2 did not influence the SEPB level in hypophysectomized males. The rate of development of the E2 effect on the SEPB level of the mature male liver increased with the growth of the dose and duration of hormone administration. The inhibitory effect of E2 was also revealed in a single administration of 10 micrograms of the hormone. In that case the effect was observed after a 3-day lag period, and a maximum decrease in the SEPB level occurred in 6 days. The regulatory negative effect of E2 was reversible. Complete regeneration of the initial SEPB content took place 10-12 days after the development of the maximum effect of E2.

摘要

采用一种差异化定量测定方法,研究了雌激素(E)在诱导和调节大鼠肝脏中特异性雌激素结合蛋白(SEBP)水平方面的作用。结果表明,在SEPB水平的初始测定中,E不能替代雄激素(A),也不能阻止其依赖A的诱导。多次给予0.4微克雌二醇(E2)会导致完整和去势雄性大鼠以及具有A诱导的SEPB水平的去卵巢雌性大鼠的SEPB水平显著降低。即使多次给予10微克E2,也不会影响垂体切除雄性大鼠的SEPB水平。E2对成熟雄性肝脏SEPB水平的影响发展速率随激素给药剂量和持续时间的增加而加快。单次给予10微克该激素也显示出E2的抑制作用。在这种情况下,效应在3天的延迟期后出现,SEPB水平在6天内出现最大降幅。E2的调节性负效应是可逆的。在E2产生最大效应后的10 - 12天,初始SEPB含量完全恢复。

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