Allcock G H, Battistini B, Fournier A, Warner T D, Vane J R
William Harvey Research Institute, St. Bartholomew's Hospital Medical College, London, UK.
J Pharmacol Exp Ther. 1995 Oct;275(1):120-6.
We have characterized the receptors mediating the mechanical responses of the isolated stomach strip to endothelin-1 (ET-1), endothelin-3 (ET-3) and the ETB-selective receptor agonists sarafotoxin 6c (SX6c) and IRL 1620. As antagonists we used BQ-123 (ETA receptor selective), BQ-788 (ETB receptor selective) and PD 145065 (ETA/ETB receptor nonselective). We have also compared the responses of the mature peptides to their precursors human big ET-1(1-38), porcine big ET-1(1-39) and big ET-3(1-41) amide. ET-1, ET-3, SX6c and IRL 1620 produced equipotent concentration-dependent contractions of the rat stomach strips that were antagonized by PD 145065 (10(-5) M) or BQ-788 (10(-5) M) but not by BQ-123 (10-5 M). This indicates that the ETB receptor mediates contractions to the endothelins in this preparation. In preparations precontracted with PGE2 (3 x 10(-8) M), ET-1, but not SX6c (both 3 x 10(-9) M), caused a transient (< 2 min) relaxation (approx. 40% of the induced tone). This relaxation was antagonized by BQ-123 (10(-5) M) but prolonged by BQ-788, and therefore mediated by ETA receptors. A single administration of 3 x 10(-7) M ET-1, ET-3, SX6c or IRL 1620 produced contractions that reached a maximal response after 1 to 3 min. The contractions were not maintained, although responses to ET-1 or ET-3 lost their tone less rapidly than those to SX6c or IRL 1620.(ABSTRACT TRUNCATED AT 250 WORDS)
我们已对介导离体胃条对内皮素 -1(ET -1)、内皮素 -3(ET -3)以及ETB选择性受体激动剂沙拉毒素6c(SX6c)和IRL 1620产生机械反应的受体进行了表征。作为拮抗剂,我们使用了BQ -123(ETA受体选择性)、BQ -788(ETB受体选择性)和PD 145065(ETA/ETB受体非选择性)。我们还比较了成熟肽与其前体人big ET -1(1 - 38)、猪big ET -1(1 - 39)和big ET -3(1 - 41)酰胺的反应。ET -1、ET -3、SX6c和IRL 1620对大鼠胃条产生了等效的浓度依赖性收缩,这些收缩可被PD 145065(10⁻⁵ M)或BQ -788(10⁻⁵ M)拮抗,但不能被BQ -123(10⁻⁵ M)拮抗。这表明在该制剂中ETB受体介导了对内皮素的收缩反应。在用前列腺素E2(3×10⁻⁸ M)预收缩的制剂中,ET -1(而非SX6c,两者均为3×10⁻⁹ M)引起短暂(<2分钟)的舒张(约为诱导张力的40%)。这种舒张被BQ -123(10⁻⁵ M)拮抗,但被BQ -788延长,因此由ETA受体介导。单次给予3×10⁻⁷ M的ET -1、ET -3、SX6c或IRL 1620会产生收缩,在1至3分钟后达到最大反应。收缩未持续,尽管对ET -1或ET -3的反应失去张力的速度比对SX6c或IRL 1620的反应慢。(摘要截断于250字)