Chahl L A
Neurosci Lett. 1985 Mar 22;55(1):35-40. doi: 10.1016/0304-3940(85)90308-8.
The effects of substance P (SP) antagonists on the atropine-sensitive and atropine-resistant responses to SP of guinea-pig isolated ileum were investigated. The atropine-resistant response to SP was the contractile response on untreated preparations, and the atropine-sensitive response was the response to high concentrations of SP (5 X 10(-7) M) on preparations desensitized to SP with a concentration of SP of 3 X 10(-7) M. The SP antagonists tested, (D-Pro2,D-Phe7,D-Trp9)-SP, (D-Pro2,D-Trp7,9)-SP, (D-Arg1,D-Pro2,D-Trp7,9,Leu11)-SP and (D-Arg1,D-Trp7,9,Leu11)-SP (spantide), did not have similar orders of potency on the atropine-sensitive and atropine-resistant responses to SP, spantide being more potent than the other antagonists on the atropine-resistant response but no more potent on the atropine-sensitive response than (D-Pro2,D-Phe7,D-Trp9)-SP or (D-Arg1,D-Pro2,D-Trp7,9,Leu11)-SP. These findings are consistent with the hypothesis that neuronal receptors for SP differ from those on smooth muscle in guinea-pig ileum.
研究了P物质(SP)拮抗剂对豚鼠离体回肠对SP的阿托品敏感和阿托品抵抗反应的影响。对SP的阿托品抵抗反应是未处理制剂上的收缩反应,而阿托品敏感反应是在对浓度为3×10(-7)M的SP脱敏的制剂上对高浓度SP(5×10(-7)M)的反应。所测试的SP拮抗剂,(D-脯氨酸2,D-苯丙氨酸7,D-色氨酸9)-SP、(D-脯氨酸2,D-色氨酸7,9)-SP、(D-精氨酸1,D-脯氨酸2,D-色氨酸7,9,亮氨酸11)-SP和(D-精氨酸1,D-色氨酸7,9,亮氨酸11)-SP(spantide),对SP的阿托品敏感和阿托品抵抗反应没有相似的效价顺序,spantide在阿托品抵抗反应上比其他拮抗剂更有效,但在阿托品敏感反应上并不比(D-脯氨酸2,D-苯丙氨酸7,D-色氨酸9)-SP或(D-精氨酸1,D-脯氨酸2,D-色氨酸7,9,亮氨酸11)-SP更有效。这些发现与以下假设一致,即豚鼠回肠中SP的神经元受体与平滑肌上的受体不同。