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血管收缩内皮素受体在脉管系统中存在差异定位的证据。

Evidence for a differential location of vasoconstrictor endothelin receptors in the vasculature.

作者信息

Moreland S, McMullen D, Abboa-Offei B, Seymour A

机构信息

Department of Pharmacology, Bristol-Myers Squibb Pharmaceutical Research Institute, Princeton, New Jersey 08543.

出版信息

Br J Pharmacol. 1994 Jun;112(2):704-8. doi: 10.1111/j.1476-5381.1994.tb13133.x.

Abstract
  1. There are at least two subtypes of vascular endothelin (ET) receptors. Stimulation of the ETA receptors on vascular smooth muscle cells leads to vasoconstriction, whereas activation of the ETB receptors on endothelial cells elicits vasodilatation. Several reports in the literature have suggested the presence of a vasoconstrictor non-ETA receptor on vascular smooth muscle which has pharmacological similarities to the ETB receptor. The present study was undertaken to determine the location of this ETB-like receptor within the vascular system. 2. Fourteen vascular smooth muscle preparations from six species were used to determine the effect of the ETA receptor antagonist, BQ-123, on concentration-response curves elicited by ET-1 and the ability of the ETB receptor agonist, sarafotoxin S6c, to cause contraction. The vessels fell into two categories. One group was sensitive to BQ-123 and insensitive to sarafotoxin S6c and, thus, probably contained ETA receptors. The other group, with vasoconstrictor ETB-like receptors, was insensitive to BQ-123 and sensitive to sarafotoxin S6c. 3. Vessels from cynomolgus monkeys, when studied in vitro, appeared to contain primarily ETA receptors, although the potency of BQ-123 was quite variable, suggesting the possibility of ETA receptor subtypes. In contrast, both ET-1 and sarafotoxin S6c, given as intravenous injections in conscious monkeys, produced transient, equipotent, and dose-related increases in blood pressure. The highest dose of sarafotoxin S6c (1 nmol kg-1, i.v.) also caused a marked secondary depressor response (-80 +/- 6 mmHg) that lasted approximately 10 min. The pressor responses suggest that the vasoconstrictor ETB-like receptors are present in cynomolgus monkeys. 4. The data suggest the presence of two distinct vasoconstrictor ET receptor subtypes on smooth muscle cells. The ETA receptors are primarily located on the high pressure side of the circulation. The vasoconstrictor ETB-like receptors appear to be concentrated on the low pressure side.
摘要
  1. 血管内皮素(ET)受体至少有两种亚型。刺激血管平滑肌细胞上的ETA受体可导致血管收缩,而激活内皮细胞上的ETB受体则会引起血管舒张。文献中的几份报告表明,血管平滑肌上存在一种血管收缩性非ETA受体,其药理学特性与ETB受体相似。本研究旨在确定这种类ETB受体在血管系统中的位置。2. 使用来自六个物种的14个血管平滑肌标本,以确定ETA受体拮抗剂BQ-123对ET-1引发的浓度-反应曲线的影响,以及ETB受体激动剂沙拉毒素S6c引起收缩的能力。这些血管分为两类。一组对BQ-123敏感,对沙拉毒素S6c不敏感,因此可能含有ETA受体。另一组具有血管收缩性类ETB受体,对BQ-123不敏感,对沙拉毒素S6c敏感。3. 食蟹猴的血管在体外研究时似乎主要含有ETA受体,尽管BQ-123的效力变化很大,提示可能存在ETA受体亚型。相比之下,在清醒的猴子中静脉注射ET-1和沙拉毒素S6c,均可产生短暂、等效且与剂量相关的血压升高。沙拉毒素S6c的最高剂量(1 nmol kg-1,静脉注射)还引起了持续约10分钟的明显继发性降压反应(-80±6 mmHg)。升压反应表明食蟹猴中存在血管收缩性类ETB受体。4. 数据表明平滑肌细胞上存在两种不同的血管收缩性ET受体亚型。ETA受体主要位于循环系统的高压侧。血管收缩性类ETB受体似乎集中在低压侧。

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