Maggi C A, Patacchini R, Meini S, Giuliani S
Pharmacology Department, A. Menarini Pharmaceuticals, Florence, Italy.
Eur J Pharmacol. 1993 Apr 28;235(2-3):309-11. doi: 10.1016/0014-2999(93)90152-8.
The selective tachykinin NK1 receptor agonists, septide ([Glp6,Pro9]substance P-(6-11)) and [Sar9]substance P sulfone, both produced concentration-dependent contraction of the circular muscle of the guinea-pig ileum (EC50 values 36 and 84 pM, respectively). The potent and selective NK1 receptor antagonist (+/-)-CP 96,345 antagonized the response to septide with significantly higher affinity than it did the response to [Sar9]substance P sulfone (pA2 values 9.24 and 8.17, respectively) without modifying the response to the selective NK2 receptor agonist, [beta-Ala8]neurokinin A-(4-10). These findings indicate that the septide-sensitive receptor in the circular muscle of the guinea-pig ileum is recognized with high affinity by the NK1 receptor selective antagonist (+/-)-CP 96,345.
选择性速激肽NK1受体激动剂septide([Glp6,Pro9]P物质-(6 - 11))和[Sar9]P物质砜,均能使豚鼠回肠环行肌产生浓度依赖性收缩(EC50值分别为36和84 pM)。强效选择性NK1受体拮抗剂(+/-)-CP 96,345拮抗septide反应的亲和力显著高于其拮抗[Sar9]P物质砜反应的亲和力(pA2值分别为9.24和8.17),且不改变对选择性NK2受体激动剂[β - Ala8]神经激肽A-(4 - 10)的反应。这些发现表明,豚鼠回肠环行肌中对septide敏感的受体可被NK1受体选择性拮抗剂(+/-)-CP 96,345高亲和力识别。