Hexum T D, Zheng J, Zhu J
Department of Pharmacology, University of Nebraska Medical Center, Omaha.
J Pharmacol Exp Ther. 1994 Oct;271(1):61-6.
Neuropeptide Y (NPY), a widely distributed peptide with varied activities, inhibits nicotinic receptor-induced [3H]norepinephrine ([3H]NE) secretion from bovine chromaffin cells. The secretion produced by membrane depolarization with high KCl concentrations or veratridine is not inhibited. Fragments of NPY, such as NPY18-36, are potent inhibitors of [3H]NE secretion, whereas [Leu31,Pro34]-NPY and peptide YY have no effect. The response to NPY18-36 is not sensitive to pertussis toxin pretreatment of chromaffin cells. NPY fragments also inhibit nicotinic receptor-induced 45Ca++ influx but not that induced by KCl or veratridine. The rank orders of potency for inhibition of [3H]NE secretion and 45Ca++ influx are the same: NPY18-36 > or = NPY26-36 > NPY13-36. NPY and NPYfree acid are weak inhibitors of secretion but not 45Ca++ influx. Moreover, the IC50s for NPY18-36 inhibition of [3H]NE secretion and 45Ca++ influx are comparable, 1.4 x 10(-6) M and 0.9 x 10(-6) M, respectively. Regression analysis produced a correlation coefficient of 0.9842 (P < .0001). It was concluded that NPY inhibits [3H]NE secretion by a modification of the nicotinic receptor-mediated increase in Ca++ influx. The characterization of the response suggests that the NPY effect is mediated by a previously undefined NPY receptor subtype that was designated Y4.
神经肽Y(NPY)是一种分布广泛、具有多种活性的肽,它可抑制烟碱受体诱导的牛嗜铬细胞分泌[3H]去甲肾上腺素([3H]NE)。高钾浓度或藜芦碱引起的膜去极化所产生的分泌不受抑制。NPY的片段,如NPY18 - 36,是[3H]NE分泌的有效抑制剂,而[Leu31,Pro34]-NPY和肽YY则无作用。嗜铬细胞经百日咳毒素预处理后,对NPY18 - 36的反应不敏感。NPY片段也抑制烟碱受体诱导的45Ca++内流,但不抑制钾离子或藜芦碱诱导的45Ca++内流。抑制[3H]NE分泌和45Ca++内流的效力等级顺序相同:NPY18 - 36≥NPY26 - 36>NPY13 - 36。NPY和NPY游离酸是分泌的弱抑制剂,但不是45Ca++内流的抑制剂。此外,NPY18 - 36抑制[3H]NE分泌和45Ca++内流的IC50值相当,分别为1.4×10(-6)M和0.9×10(-6)M。回归分析得出相关系数为0.9842(P<0.0001)。得出的结论是,NPY通过改变烟碱受体介导的Ca++内流增加来抑制[3H]NE分泌。该反应的特征表明,NPY的作用是由一种先前未定义的NPY受体亚型介导的,该亚型被命名为Y4。