QUININE BLOCKS THE HIGH CONDUCTANCE, CALCIUM-ACTIVATED POTASSIUM CHANNEL IN RAT PANCREATIC BETA-CELLS

被引:26
作者
MANCILLA, E
ROJAS, E
机构
[1] Laboratory of Cell Biology and Genetics, NIDDK, National Institutes of Health, Bethesda
关键词
Potassium-channel; Ca[!sup]2+[!/sup][!sub]i[!/sub]-activated; Quinine; β-Cell;
D O I
10.1016/0014-5793(90)80078-W
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
The [Ca2+]i-activated K+-channel, one of the 3 K+-channels described in pancreatic β-cells, is a high conductance, voltage-dependent K+-channel. Quinine, known to block [Ca2+]i-activated K+-channels in other cells, has been described to block the silent phase between the bursts of glucose-evoked electrical activity in mouse pancreatic β-cells, and to inhibit K+ efflux from rat pancreatic islets. We report here that quinine blocks the [Ca2+i-activated K+-channel in rat pancreatic β-cells, from the external side of the membrane. We also show that the blockade is characterized by fast flickering of the K+-channel between the open and closed state. Mean open and closed times within bursts were found to be exponentially distributed, suggesting that the blockade by quinine involves obstruction on the K+ flow through the open to be exponentially distributed, suggesting that the blockade by quinine involves obstruction on the K+ flow through the open channel. © 1990.
引用
收藏
页码:105 / 108
页数:4
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