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5-羟色胺2(5-HT2)能受体拮抗剂酮色林与α1肾上腺素能受体拮抗剂特拉唑嗪在麻醉兔体内血管舒张作用的差异。

Differences in vasodilating action between ketanserin, a 5-HT2-serotonergic receptor antagonist, and terazosin, an alpha 1-adrenoceptor antagonist, in anesthetized rabbits.

作者信息

Ikeda K, Takata M, Tomoda F, Mikawa M, Iida H, Sasayama S

机构信息

Second Department of Internal Medicine, Faculty of Medicine, Toyama Medical and Pharmaceutical University, Japan.

出版信息

J Cardiovasc Pharmacol. 1987;10 Suppl 3:S69-72.

PMID:2446076
Abstract

It has not yet been demonstrated clearly whether the antihypertensive action of ketanserin is due to 5-hydroxytryptamine type-2 (5-HT2)-serotonergic receptor blockade or to alpha 1-adrenergic receptor blockade. The present study was performed to evaluate in vivo the antihypertensive action of ketanserin in comparison with that of terazosin, a selective alpha 1-adrenoceptor antagonist. The changes of renal blood flow (RBF) after intrarenal injection of phenylephrine, 5-HT, or angiotensin II were measured in anesthetized rabbits. RBF responses induced by these vasoconstrictors with or without pretreatment with ketanserin (0.2, 1.0, and 5.0 mg/kg, i.v.) or terazosin (0.04, 0.2, and 1.0 mg/kg, i.v.) were examined. Following intrarenal injection, RBF decreased by 20.8%, 22.7%, and 23.0% respectively, without ketanserin and also decreased by 21.0%, 21.6%, and 24.4%, respectively, without terazosin. Following pretreatment with a small dose of ketanserin or terazosin, the vasoconstricting effects of phenylephrine were attenuated by 20% or 62% (delta% changes in RBF), respectively. The effects of 5-HT on RBF responsiveness were blocked by ketanserin in a dose-dependent manner. Ketanserin did not modify the RBF responses to angiotensin II. These findings indicate that the antihypertensive effect of ketanserin, to a certain extent, depends on the blockade of the 5-HT2-serotonergic receptor in addition to that of the alpha 1-adrenoceptor, whereas the renin-angiotensin system is not involved in the hypotensive effects of ketanserin.

摘要

酮色林的降压作用究竟是由于对5-羟色胺2型(5-HT2)-血清素能受体的阻断还是对α1-肾上腺素能受体的阻断,目前尚未明确证实。本研究旨在通过体内实验评估酮色林与选择性α1-肾上腺素能受体拮抗剂特拉唑嗪相比的降压作用。在麻醉的兔子身上测量肾内注射去氧肾上腺素、5-羟色胺或血管紧张素II后肾血流量(RBF)的变化。检测了在使用或不使用酮色林(0.2、1.0和5.0毫克/千克,静脉注射)或特拉唑嗪(0.04、0.2和1.0毫克/千克,静脉注射)预处理的情况下,这些血管收缩剂诱导的RBF反应。肾内注射后,在未使用酮色林时RBF分别下降了20.8%、22.7%和23.0%,在未使用特拉唑嗪时也分别下降了21.0%、21.6%和24.4%。用小剂量酮色林或特拉唑嗪预处理后,去氧肾上腺素的血管收缩作用分别减弱了20%或62%(RBF变化的百分比差值)。5-羟色胺对RBF反应性的影响被酮色林以剂量依赖的方式阻断。酮色林未改变RBF对血管紧张素II的反应。这些发现表明,酮色林的降压作用在一定程度上除了依赖于对α1-肾上腺素能受体的阻断外,还依赖于对5-HT2-血清素能受体的阻断,而肾素-血管紧张素系统不参与酮色林的降压作用。

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