Parlani M, Conte B, Cirillo R, Manzini S
Pharmacology Department, Menarini Ricerche, Pomezia (Roma), Italy.
Eur J Pharmacol. 1996 Dec 30;318(2-3):419-24. doi: 10.1016/s0014-2999(96)00799-6.
The nature of the tachykinin receptors involved in the contraction of the circular muscle of dog colon has been investigated. The following rank order of potency for agonists was obtained: [Sar9,Met(O2)11]substance P > or = neurokinin A > [beta-Ala8]neurokinin A-(4-10) >> [MePhe7]neurokinin B. The efficacy of the tachykinin NK2 receptor agonists was significantly greater than that of the tachykinin NK1 receptor agonists and of carbachol. A concentration-dependent rightward shift of the motor response to neurokinin A (obtained in the presence of (+/-)-CP 96,345) was induced by peptide and non-peptide tachykinin NK2 receptor antagonists with this rank order: MEN 10,627 = SR 48,968 >> L 659,877 > MEN 10,376 > MDL 28,564. MEN 10,627 and SR 48,968 affinities were similar to those measured in human tissues. In conclusion, the tachykinin NK2 receptor plays a predominant role in tachykinin-induced contraction of the canine colonic circular muscle and this tissue could be useful to predict the pharmacological actions of MEN 10,627 and SR 48,968 in human colon.
对参与犬结肠环行肌收缩的速激肽受体的性质进行了研究。获得了以下激动剂的效价顺序:[Sar9,Met(O2)11]P物质≥神经激肽A>[β-丙氨酸8]神经激肽A-(4-10)>>[甲基苯丙氨酸7]神经激肽B。速激肽NK2受体激动剂的效力显著大于速激肽NK1受体激动剂和卡巴胆碱。肽类和非肽类速激肽NK2受体拮抗剂以以下顺序诱导对神经激肽A的运动反应(在(±)-CP 96,345存在下获得)浓度依赖性右移:MEN 10,627 = SR 48,968>>L 659,877>MEN 10,376>MDL 28,564。MEN 10,627和SR 48,968的亲和力与在人体组织中测得的相似。总之,速激肽NK2受体在速激肽诱导的犬结肠环行肌收缩中起主要作用,该组织可能有助于预测MEN 10,627和SR 48,968在人体结肠中的药理作用。