Tachykinin-induced contraction of the guinea-pig isolated oesophageal mucosa is mediated by NK2 receptors

被引:9
|
作者
Kerr, KP [1 ]
Thai, B [1 ]
Coupar, IM [1 ]
机构
[1] Monash Univ, Victorian Coll Pharm, Dept Pharmaceut Biol & Pharmacol, Parkville, Vic 3052, Australia
关键词
guinea-pig oesophagus; tachykinin NK2 receptors; muscularis mucosae; NKA; Nle(10)]-NKA(4-10); GR 64,349; senktide; SR 48,968; GR 159,897;
D O I
10.1038/sj.bjp.0703708
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1 The tachykinin receptor present in the guinea-pig oesophageal mucosa that mediates contractile responses of the muscularis mucosae has been characterized, using functional in vitro experiments. 2 The NK1 receptor-selective agonist, [Sar(9)(O-2)Met(11)]SP and the NK3 receptor-selective agonists, [MePhe(7)]-NKB and senktide, produced no response at submicromolar concentrations. The NK2 receptor-selective agonists, [Nle(10)]-NKA(4-10), and GR 64,349 produced concentration-dependent contractile effects with pot values of 8.20+/-0.16 and 8.30+/-0.15, respectively. 3 The concentration-response curve to the non-selective agonist, NKA (pD(2)=8.13+/-0.04) was shifted significantly rightwards only by the NK2 receptor-selective antagonist, GR 159.897 and was unaffected by the NK1 receptor-selective antagonist, SR 140,333 and the NK3 receptor-selective antagonist, SE 222,200. 4 The NK2 receptor-selective antagonist, GR 159,897, exhibited an apparent competitive antagonism against the NK2 receptor-selective agonist, GR 64,349 (apparent pK(B) value = 9.29 +/- 0.16) and against the non-selective agonist, NKA (apparent pK(B) value = 8.71 +/- 0.19). 5 The NK2 receptor-selective antagonist. SR 48,968 exhibited a non-competitive antagonism against the NK1 receptor-selective agonist, [Nle(10)]-NKA(4-10). The pK(B) value was 10.84+/-0.19. 6 It is concluded that the guinea-pig isolated oesophageal mucosa is a useful preparation for studying the effects of NK2 receptor-selective agonists and antagonists as the contractile responses to Various tachykinins are mediated solely by NK2 receptors.
引用
收藏
页码:1461 / 1467
页数:7
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