ANESTHETIC PHENCYCLIDINE, BLOCKER OF THE ATP-SENSITIVE POTASSIUM CHANNELS

被引:8
作者
KOKOZ, YM
ALEKSEEV, AE
POVZUN, AA
KORYSTOVA, AF
PERESSAAD, H
机构
[1] Laboratory of Functional Biochemistry, Institute of Theoretical and Experimental Biophysics, Russian Academy of Sciences, Pushchino
关键词
ATP-SENSITIVE K-CHANNEL; PHENCYCLIDINE; CALCIUM CURRENT; CARDIOMYOCYTE; PATCH CLAMP;
D O I
10.1016/0014-5793(94)80208-4
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 double sucrose gap and patch-clamp studies revealed that phencyclidine blocked the ATP-sensitive K+ channel in isolated cardiac cells (half-maximal inhibition at approximate to 20 mu M; Hill coefficient approximate to 1). 10 mu M phencyclidine increased the inward Ca2+ current and blocked the outward K+ current in the frog auricle trabeculae. The phencyclidine effects on the frog auricle trabeculae and the isolated cardiac cells proved to be quite reversible.
引用
收藏
页码:277 / 280
页数:4
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