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[促卵泡激素分泌对垂体中性激素受体水平及中枢神经系统儿茶酚胺能系统活性的依赖性]

[The dependence of follicle-stimulating hormone secretion on the level of sex hormone receptors in the hypophysis and on the activity of the CNS catecholaminergic systems].

作者信息

Babichev V N, Peryshkova T A, Adamskaia E I

出版信息

Probl Endokrinol (Mosk). 1990 May-Jun;36(3):53-7.

PMID:2118637
Abstract

A study was made of the influence of agonists and antagonists of catecholamine action on LH and FSH secretion during the second rise of FSH secretion at the early hours of the estrous stage (E). Administration of phentolamine (a blocker of alpha-adrenoceptors) did not change the level of gonadotropins. On the contrary, haloperidol (a blocker of dopamine receptors) lowered the level of FSH at 3 o'clock of the estrous stage but made no effect on the blood concentration of LH. Administration of a stimulator of dopamine receptors increased the blood concentration of FSH at 1 and 3 o'clock of the estrous stage. Acute administration of haloperidol decreased the number of nuclear estradiol-binding sites in the adenohypophysis at 3 o'clock of the estrous stage but did not change the concentration of nuclear receptors of testosterone at either of the above time intervals. The results suggest that estrogenic and androgenic receptors and dopamine cerebral systems are involved in the stimulation of the second wave of FSH secretion. The interrelation of the dopamine activity and level of hypophyseal estradiol receptors, influencing FSH secretion in the early estrus, was established.

摘要

一项关于在发情期(E)早期促卵泡激素(FSH)分泌第二次上升期间,儿茶酚胺作用的激动剂和拮抗剂对促黄体生成素(LH)和FSH分泌影响的研究。给予酚妥拉明(一种α-肾上腺素能受体阻滞剂)并未改变促性腺激素水平。相反,氟哌啶醇(一种多巴胺受体阻滞剂)降低了发情期3点时FSH的水平,但对LH的血浓度没有影响。给予多巴胺受体刺激剂可提高发情期1点和3点时FSH的血浓度。发情期3点时急性给予氟哌啶醇可减少腺垂体中核雌二醇结合位点的数量,但在上述任何一个时间间隔内均未改变睾酮核受体的浓度。结果表明,雌激素和雄激素受体以及多巴胺脑系统参与了FSH分泌第二波的刺激。确定了影响发情早期FSH分泌的多巴胺活性与垂体雌二醇受体水平之间的相互关系。

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