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神经肽Y通过多个位点抑制蛋白激酶C刺激的人结肠癌细胞系HT29cl.19A细胞系中的氯离子分泌。

Neuropeptide Y inhibits the protein kinase C-stimulated Cl(-) secretion in the human colonic cell line HT29cl.19A cell line via multiple sites.

作者信息

Oprins J C, Bouritius H, Bajnath R B, Groot J A

机构信息

Swammerdam Institute for Life Sciences, University of Amsterdam, P.O. Box 94084, 1090 GB, Amsterdam, Netherlands.

出版信息

Eur J Pharmacol. 2001 Mar 23;416(1-2):43-50. doi: 10.1016/s0014-2999(01)00869-x.

Abstract

Neuropeptide Y is known to exert inhibitory effects on ion secretion in the intestine by reducing the activity of adenylyl cyclase. In the human intestinal epithelial cell line HT29cl.19A, it has been previously shown that neuropeptide Y inhibits the electrophysiological phenomena related to Cl(-) secretion, when induced by elevation of cAMP via forskolin. Moreover, the secretion induced via elevation of intracellular calcium levels via muscarinic activation can be inhibited by neuropeptide Y. Part of these inhibitions appeared to be due to lowered calcium activity in the epithelial cells, thereby reducing the basolateral K(+) conductance. The phorbol ester 4-phorbol-12,13-dibutyrate (PDB) can induce secretion in this cell line via activation of protein kinase C as well; however, the effect of neuropeptide Y on this pathway has not yet been studied. In the present experiments, it is shown that neuropeptide Y inhibits the PDB-induced secretion at two sides: one located in the apical membrane and another in the basolateral membrane. It is shown that the latter effect can, at least partially, be explained via a direct effect of neuropeptide Y on the K(+) conductance. This was concluded from the observation that neuropeptide Y could also reduce basolateral K(+) conductance when intracellular calcium was dramatically increased by ionomycin. The observed inhibitory effects suggest that neuropeptide Y is a very powerful antisecretory peptide in human intestinal epithelial cells.

摘要

已知神经肽Y通过降低腺苷酸环化酶的活性对肠道离子分泌发挥抑制作用。在人肠上皮细胞系HT29cl.19A中,先前已表明,当通过福斯可林升高cAMP诱导时,神经肽Y抑制与Cl(-)分泌相关的电生理现象。此外,通过毒蕈碱激活使细胞内钙水平升高所诱导的分泌可被神经肽Y抑制。这些抑制作用部分似乎是由于上皮细胞中钙活性降低,从而降低了基底外侧K(+)电导。佛波酯4-佛波醇-12,13-二丁酸酯(PDB)也可通过激活蛋白激酶C在该细胞系中诱导分泌;然而,神经肽Y对该途径的作用尚未得到研究。在本实验中,表明神经肽Y在两个方面抑制PDB诱导的分泌:一个位于顶端膜,另一个位于基底外侧膜。结果表明,后一种作用至少部分可通过神经肽Y对K(+)电导的直接作用来解释。这是从以下观察结果得出的结论:当用离子霉素使细胞内钙显著增加时,神经肽Y也可降低基底外侧K(+)电导。观察到的抑制作用表明神经肽Y在人肠上皮细胞中是一种非常强大的抗分泌肽。

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