Taoudi Benchekroun M, St-Pierre S, Fournier A, Cadieux A
Department of Pharmacology, Faculty of Medicine, University of Sherbrooke, Quebec, Canada.
Br J Pharmacol. 1993 Aug;109(4):902-4. doi: 10.1111/j.1476-5381.1993.tb13705.x.
The C-terminal fragment of neuropeptide Y (NPY), NPY(2-36) was used as a means of discriminating between two differently located NPY receptor sites in guinea-pig trachea. Both NPY and NPY(2-36) reduced the maximal relaxation elicited by vasoactive intestinal peptide (VIP). In contrast, the C-terminal fragment did not mimic the inhibitory action of NPY on the noradrenaline-(NA) evoked response. However, pretreatment of the trachea with 30 nM NPY(2-36), 5 min before generating NA and VIP concentration-response curves in the presence of NPY, abolished the inhibitory effect of NPY on NA-elicited response but did not affect the modulatory action of NPY on VIP-induced relaxation. These results suggest that the two differently located NPY receptor sites in guinea-pig trachea are of two distinct subpopulations.
神经肽Y(NPY)的C末端片段NPY(2 - 36)被用作区分豚鼠气管中两个不同位置的NPY受体位点的一种手段。NPY和NPY(2 - 36)均降低了血管活性肠肽(VIP)引起的最大舒张。相反,C末端片段并未模拟NPY对去甲肾上腺素(NA)诱发反应的抑制作用。然而,在存在NPY的情况下生成NA和VIP浓度 - 反应曲线前5分钟,用30 nM NPY(2 - 36)预处理气管,消除了NPY对NA诱发反应的抑制作用,但不影响NPY对VIP诱导舒张的调节作用。这些结果表明,豚鼠气管中两个不同位置的NPY受体位点属于两个不同的亚群。