Suppr超能文献

兔基底动脉中的激肽受体与血管紧张素转换酶

Kinin receptors and angiotensin converting enzyme in rabbits basilar arteries.

作者信息

Whalley E T, Fritz H, Geiger R

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1983 Dec;324(4):296-301. doi: 10.1007/BF00502627.

Abstract

Bradykinin (BK) initially produced concentration related relaxations of the rabbit basilar artery in vitro under resting tension and when contracted with 5-hydroxytryptamine. Concentration-effect (C-E) curves to BK repeated at 2 h intervals over an 8-10 h period resulted in the production of progressively increased contractile responses. The induction of these contractile responses to BK was prevented by pre-incubation of these tissues with cycloheximide. On tissues which had been challenged with BK at 2 h intervals for 8 h in the absence of cycloheximide the rank order of potency of three kinins to produce contraction was methionyl-lysyl-BK (M-L-BK) greater than BK greater than des-Arg9-BK. On the same tissues the specific B1-receptor antagonist des-Arg9-Leu8-BK inhibited the contractile effects of BK. These results suggest the presence of a B1-receptor mediating contraction. The rank order of potency of the kinins to produce relaxation of tissues preincubated with cycloheximide was BK greater than M-L-BK greater than des-Arg9-BK which suggests the presence of a B2-receptor mediating these responses. Angiotensin I (AI) and angiotensin II (AII) produced concentration related contractions of the tissue. The angiotensin converting enzyme inhibitors captopril, BPP5a and BPP9a inhibited responses to AI but had no effect on contractile C-E curves to BK, AII and 5-HT or on relaxant C-E curves to BK. These results suggest that the rabbit basilar artery in vitro contains two BK receptors, a B1 receptor mediating contraction and a B2 receptor mediating relaxation.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

缓激肽(BK)最初在体外对处于静息张力下以及用5-羟色胺收缩后的兔基底动脉产生浓度相关的舒张作用。在8 - 10小时内以2小时间隔重复进行的BK浓度-效应(C-E)曲线实验导致产生逐渐增强的收缩反应。用环己酰亚胺预孵育这些组织可防止对BK产生这些收缩反应。在未用环己酰亚胺的情况下,以2小时间隔用BK刺激8小时的组织上,三种激肽产生收缩作用的效价顺序为:甲硫氨酰-赖氨酰-BK(M-L-BK)>BK>去-精氨酸9 - BK。在相同组织上,特异性B1受体拮抗剂去-精氨酸9 - 亮氨酸8 - BK抑制了BK的收缩作用。这些结果提示存在介导收缩作用的B1受体。在用环己酰亚胺预孵育的组织中,激肽产生舒张作用的效价顺序为:BK>M-L-BK>去-精氨酸9 - BK,这提示存在介导这些反应的B2受体。血管紧张素I(AI)和血管紧张素II(AII)对该组织产生浓度相关的收缩作用。血管紧张素转换酶抑制剂卡托普利、BPP5a和BPP9a抑制对AI的反应,但对BK、AII和5 - HT的收缩C-E曲线或BK的舒张C-E曲线无影响。这些结果表明,体外兔基底动脉含有两种BK受体,一种介导收缩的B1受体和一种介导舒张的B2受体。(摘要截短于250字)

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验