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神经垂体肽的利钠作用:激动剂和拮抗剂的作用以及利钠受体的意义

Natriuretic action of neurohypophysial peptides: effects of agonists and antagonists and implication of natriuretic receptor.

作者信息

Chan W Y, Hruby V J

机构信息

Department of Pharmacology, Cornell University Medical College, New York, New York.

出版信息

J Pharmacol Exp Ther. 1988 Aug;246(2):597-602.

PMID:2969979
Abstract

Neurohypophysial peptides possess natriuretic activity. Although it has been shown that the natriuretic action of these peptides can be dissociated from their antidiuretic activity (a V2-receptor mediated response), it is not known whether the V1-receptor or yet a third receptor type mediates the natriuretic response. Also, it has not been studied what effects V1- and V2-antagonists may have on urinary sodium excretion. To define this, we have studied the effects of four oxytocin (OT) agonists: arginine-vasopressin, OT, [Leu4]OT and [cyclo-Leu8]OT; two V1-receptor antagonists: [penicillamine1,Phe(Methyl)2,Thr4,Orn8]OT and [penicillamine1,D-Phe(Ethyl)2,Thr4,Orn8]OT and one V2-receptor antagonist: d-(CH2)5[D-Ile2,alpha-aminobutyric acid4]arginine-vasopressin on renal excretion of water and electrolytes in anesthetized rats under water diuresis. We also studied the effects of the antagonists on the OT-induced antidiuretic and natriuretic responses. Only the agonists, but not the antagonists, were found to have natriuretic activity. The natriuretic potency was not related to the peptide's antidiuretic activity, but was in the same rank order as their oxytocic activity (a V1-agonist effect). The effects of the antagonists on the OT-induced renal responses were studied at two dose levels, representing a strong and near maximal of their respective V1 and V2 inhibitory doses. The V1-antagonist had no effect on the antidiuretic response to OT but inhibited the natriuretic response in a dose-dependent manner. The antinatriuretic effect was also long-lasting as its antioxytocic activity. The V2-antagonist inhibited the antidiuretic response to OT in a dose-dependent manner but only the high dose inhibited the natriuretic response. These results indicate that the natriuretic action of OT was not mediated by V2-receptors and antinatriuresis was not specific for V1-antagonist.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

神经垂体肽具有利钠活性。尽管已经表明这些肽的利钠作用可与其抗利尿活性(一种V2受体介导的反应)相分离,但尚不清楚是V1受体还是第三种受体类型介导利钠反应。此外,尚未研究V1和V2拮抗剂对尿钠排泄可能有何影响。为了明确这一点,我们研究了四种催产素(OT)激动剂:精氨酸加压素、OT、[亮氨酸4]OT和[环亮氨酸8]OT;两种V1受体拮抗剂:[青霉胺1,苯丙氨酸(甲基)2,苏氨酸4,鸟氨酸8]OT和[青霉胺1,D-苯丙氨酸(乙基)2,苏氨酸4,鸟氨酸8]OT,以及一种V2受体拮抗剂:d-(CH2)5[D-异亮氨酸2,α-氨基丁酸4]精氨酸加压素对水负荷利尿状态下麻醉大鼠肾水和电解质排泄的影响。我们还研究了拮抗剂对OT诱导的抗利尿和利钠反应的影响。仅发现激动剂具有利钠活性,而拮抗剂没有。利钠效力与肽的抗利尿活性无关,但与它们的催产活性(一种V1激动剂效应)处于相同的等级顺序。在两个剂量水平研究了拮抗剂对OT诱导的肾反应的影响,这两个剂量分别代表其各自V1和V2抑制剂量的强效和接近最大剂量。V1拮抗剂对OT的抗利尿反应没有影响,但以剂量依赖的方式抑制利钠反应。抗利钠作用也与其抗催产活性一样持久。V2拮抗剂以剂量依赖的方式抑制OT的抗利尿反应,但只有高剂量抑制利钠反应。这些结果表明,OT的利钠作用不是由V2受体介导的,抗利钠作用对V1拮抗剂也不具有特异性。(摘要截断于250字)

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