Torrens Y, Dietl M, Beaujouan J C, Glowinski J
Collège de France, Chaire de Neuropharmacologie, I.N.S.E.R.M. n. U 114, Paris.
C R Acad Sci III. 1989;309(8):295-9.
The stimulation of rat parotid acinar cells by substance P(SP) resulted in a significant reduction in the initial accumulation of cytosolic myo[3H]inositol and in the initial labelling of phosphoinositides. The SP-induced reduction was concentration-dependent, the EC50 of SP was 5.8 +/- 2.5 nM. Spantide, [D-Arg1, D-Trp7,9, Leu11]SP, a SP antagonist, used at a concentration of 10(-5) M, competitively shifted the dose-response curve of SP. The pharmacological analysis of the effects of several tachykinins and analogues, suggests the implication of NK1 receptors (specific receptor of SP).
P物质(SP)对大鼠腮腺腺泡细胞的刺激导致胞质肌醇[3H]肌醇初始积累量以及磷酸肌醇初始标记量显著降低。SP诱导的降低呈浓度依赖性,SP的半数有效浓度(EC50)为5.8±2.5 nM。SP拮抗剂[D-精氨酸1,D-色氨酸7,9,亮氨酸11]SP(spantide)以10⁻⁵ M的浓度使用时,竞争性地改变了SP的剂量反应曲线。对几种速激肽及其类似物作用的药理学分析表明,NK1受体(SP的特异性受体)参与其中。