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[组胺作为雌二醇对大鼠子宫作用的中介物的作用:使用组胺拮抗剂抑制激素诱导的酶]

[Role of histamine as an intermediary in the action of estradiol on the rat uterus: inhibition of the hormonal induction of enzymes using histamine antagonists].

作者信息

Pankova T G, Igonina T M, Salganik R I

出版信息

Probl Endokrinol (Mosk). 1985 May-Jun;31(3):73-8.

PMID:2865726
Abstract

The administration of methiamide, a blocker of histamine H2-receptors, to rats was shown to prevent the induction of hexokinase (HK) and glucose-6-phosphate dehydrogenase (G-6PD) caused by both histamine and estradiol. An inhibitory effect of methiamide remained stable up to 16 h after histamine and estradiol administration. Diphenhydramine, a blocker of histamine H1-receptors, produces a short-term inhibitory effect on the HK and G-6PD activity stimulated by histamine and estradiol. The short-term nature of the diphenhydramine effect may be attributed to a low affinity to histamine H2-receptors and histamine fast dissociation. It may be concluded that some of the estradiol effects, particularly the HK and G-6PD induction in the uterus are histamine-mediated, apparently by means of H2-receptors. The administration of histamine to rats increases the uterus mass causing its inundation, and H1- and H2-blockers prevent this effect of histamine. However, the above histamine antagonists do not inhibit uterus inundation caused by estradiol. A conclusion is made that estradiol stimulates the uterus inundation not only by means of histamine but also by some other means.

摘要

对大鼠施用组胺H2受体阻滞剂甲硫酰胺,可预防由组胺和雌二醇引起的己糖激酶(HK)和葡萄糖-6-磷酸脱氢酶(G-6PD)的诱导。在施用组胺和雌二醇后长达16小时,甲硫酰胺的抑制作用保持稳定。组胺H1受体阻滞剂苯海拉明对由组胺和雌二醇刺激的HK和G-6PD活性产生短期抑制作用。苯海拉明作用的短期性质可能归因于对组胺H2受体的低亲和力和组胺的快速解离。可以得出结论,雌二醇的一些作用,特别是子宫中HK和G-6PD的诱导是由组胺介导的,显然是通过H2受体。给大鼠施用组胺会增加子宫重量并导致其充血,而H1和H2阻滞剂可预防组胺的这种作用。然而,上述组胺拮抗剂并不抑制由雌二醇引起的子宫充血。得出的结论是,雌二醇不仅通过组胺而且还通过其他一些方式刺激子宫充血。

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