G-PROTEIN ACTIVATION - A RECEPTOR-INDEPENDENT MODE OF ACTION FOR CATIONIC AMPHIPHILIC NEUROPEPTIDES AND VENOM PEPTIDES

被引:422
作者
MOUSLI, M [1 ]
BUEB, JL [1 ]
BRONNER, C [1 ]
ROUOT, B [1 ]
LANDRY, Y [1 ]
机构
[1] CNRS,CTR PHARMACOL ENDOCRINOL,INSERM,F-34094 MONTPELLIER 2,FRANCE
关键词
D O I
10.1016/0165-6147(90)90179-C
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The neuropeptide substance P, the venom peptide mastoparan and the synthetic polyamine compound 48/80 activate rat peritoneal mast cells, leading to rapid histamine release by exocytosis. Although these effects are inhibited by pertussis toxin and involve a transient increase in IP3, no selective membrane receptors have been identified. However, it has recently been shown that these compounds activate G proteins in vitro. Here Yves Landry and colleagues discuss the proposal that direct activation of G protein is the physiological mechanism of action of substance P on rat peritoneal mast cells, this mechanism being mimicked by mastoparan and 48/80, and possibly by other cationic amphiphilic peptides such as kinins. These compounds might be of help m defining the interaction between membrane receptors and G proteins. © 1990.
引用
收藏
页码:358 / 362
页数:5
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