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人冠状动脉中内皮素受体分布存在异质性的证据。

Evidence for heterogeneity of endothelin receptor distribution in human coronary artery.

作者信息

Godfraind T

机构信息

Laboratoire de Pharmacologie, Université Catholique de Louvain, Brussels, Belgium.

出版信息

Br J Pharmacol. 1993 Nov;110(3):1201-5. doi: 10.1111/j.1476-5381.1993.tb13942.x.

Abstract
  1. The receptors mediating endothelin-evoked contraction of human coronary artery have been investigated in isolated segments of the left anterior descending coronary artery (LAD). 2. Endothelin-1 (ET-1) was 10 times more potent in distal than in proximal segments but the potency ratio between ET-1 and ET-3 (endothelin-3) was similar and close to 100 in any segment of the artery. 3. BQ-123, an ETA receptor antagonist, competitively antagonized the response to ET-1 of distal segments (pA2 equal to 7.47). In the proximal segments, part of the contractile response was BQ123 sensitive, but the antagonism was non-competitive. In both groups of segments, the response to ET-3 could be completely blocked by BQ-123. 4. These observations indicate that ETA receptors mediate the contractile response to ET-1 in distal, pre-resistant coronary arteries, but that other ET receptors are also involved in the contractile response of proximal segments.
摘要
  1. 已在离体左冠状动脉前降支(LAD)节段中研究了介导内皮素诱发人冠状动脉收缩的受体。2. 内皮素-1(ET-1)在远端节段的效力比近端节段高10倍,但在动脉的任何节段中,ET-1与内皮素-3(ET-3)之间的效力比相似且接近100。3. ETA受体拮抗剂BQ-123竞争性拮抗远端节段对ET-1的反应(pA2等于7.47)。在近端节段,部分收缩反应对BQ123敏感,但拮抗作用是非竞争性的。在两组节段中,对ET-3的反应均可被BQ-123完全阻断。4. 这些观察结果表明,ETA受体介导远端、抗药前冠状动脉对ET-1的收缩反应,但其他ET受体也参与近端节段的收缩反应。

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本文引用的文献

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Some quantitative uses of drug antagonists.药物拮抗剂的一些定量应用。
Br J Pharmacol Chemother. 1959 Mar;14(1):48-58. doi: 10.1111/j.1476-5381.1959.tb00928.x.
2
Endothelins--from receptors to medicine.内皮素——从受体到医学
Trends Pharmacol Sci. 1993 Feb;14(2):54-60. doi: 10.1016/0165-6147(93)90031-e.

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