Naranjo J R, Arnedo A, De Felipe M C, Del Rio J
Peptides. 1986 May-Jun;7(3):419-23. doi: 10.1016/0196-9781(86)90008-2.
Substance P (SP), physalaemin, SP4-11, SP5-11 and the SP5-11 analog DiMe-C7 induce an antinociceptive effect in rats after intraventricular administration. Other tachykinins and the N-terminal fragments of SP are inactive. All antinociceptive peptides increase the Met-enkephalin efflux from slices of rat periaqueductal gray matter and their antinociceptive potency is correlated with their capacity to release Met-enkephalin. The results, discussed in the light of current theories on different tachykinin receptors, suggest that the SP-P receptor subtype may be involved in the control of noxious stimulation elicited by SP at supraspinal levels.
P物质(SP)、雨蛙肽、SP4 - 11、SP5 - 11以及SP5 - 11类似物DiMe - C7在脑室内给药后可在大鼠中诱导出抗伤害感受作用。其他速激肽以及SP的N端片段无活性。所有抗伤害感受肽均可增加大鼠导水管周围灰质切片中甲硫氨酸脑啡肽的外流,且它们的抗伤害感受效力与其释放甲硫氨酸脑啡肽的能力相关。根据当前关于不同速激肽受体的理论对这些结果进行讨论,提示SP - P受体亚型可能参与脊髓上水平由SP引发的伤害性刺激的控制。