ENHANCEMENT OF BETA-ADRENERGIC-RECEPTOR ACTIVATION OF MAXI-K+ CHANNELS BY GM1 GANGLIOSIDE

被引:6
作者
FAN, SF [1 ]
WANG, SY [1 ]
KAO, CY [1 ]
机构
[1] SUNY HLTH SCI CTR,DEPT PHARMACOL,BROOKLYN,NY 11203
关键词
D O I
10.1006/bbrc.1994.1598
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In freshly dispersed guinea-pig taenia coli myocytes, beta-adrenergic receptor agonist increased the open probability (p(o)) of the maxi-K+ channels through the G-protein, G. Subunit B of cholera toxin (0.1 nM) suppressed the ISO-induced increase of p(o) of maxi-K-s+ channels but did not affect that induced by forskolin. Brief (20 min) treatment of the myocytes with GM1 ganglioside (GM1, 0.1-1.0 mu M) enhanced the effectiveness of ISO-induced increase of p(o). This effect was blocked by 0.5% trypsin, which is known to prevent the incorporation of exogeneous GM1 into the membrane. The effect of GM1 was not shared by GM2 and GM3 gangliosides. These results suggest that the membrane-bound endogeneous GM1 may participate in the regulation of cellular response to beta-adrenergic agents. (C) 1994 Academic Press, Inc.
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页码:1341 / 1345
页数:5
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