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ω-芋螺毒素GVIA可抑制大鼠下丘脑切片释放组胺,但二氢吡啶衍生物尼伐地平则无此作用。

Inhibition of histamine release from rat hypothalamic slices by omega-conotoxin GVIA, but not by nilvadipine, a dihydropyridine derivative.

作者信息

Takemura M, Kishino J, Yamatodani A, Wada H

机构信息

Department of Pharmacology II, Faculty of Medicine, Osaka University, Japan.

出版信息

Brain Res. 1989 Sep 4;496(1-2):351-6. doi: 10.1016/0006-8993(89)91087-1.

Abstract

Histamine release in response to 40 mM high K+-stimulation from the rat hypothalamic slice preparations perifused in vitro was significantly inhibited by 1.0 nM-1.0 microM omega-conotoxin GVIA, a peptide modulator of N- and L-type voltage-sensitive calcium channels, but not by similar concentrations of nilvadipine, a dihydropyridine derivative of L-type calcium channel antagonist. These results indicate that the voltage-sensitive calcium channel controlling histamine release from hypothalamic slices is omega-conotoxin-sensitive but dihydropyridine-insensitive.

摘要

在体外灌流的大鼠下丘脑切片标本中,1.0 nM - 1.0 μM的ω-芋螺毒素GVIA(一种N型和L型电压敏感性钙通道的肽调节剂)可显著抑制由40 mM高钾刺激引起的组胺释放,但相似浓度的尼伐地平(一种L型钙通道拮抗剂的二氢吡啶衍生物)则无此作用。这些结果表明,控制下丘脑切片组胺释放的电压敏感性钙通道对ω-芋螺毒素敏感,但对二氢吡啶不敏感。

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