Sulfhydryl redox modulates ATP-sensitive K+ channels in rabbit ventricular myocytes

被引:18
作者
Han, J [1 ]
Kim, E [1 ]
Ho, WK [1 ]
Earm, YE [1 ]
机构
[1] INJE UNIV,COLL MED,DEPT PHYSIOL & BIOPHYS,KIMHAE,SOUTH KOREA
关键词
D O I
10.1006/bbrc.1996.0330
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 properties of sulfhydryl redox modulation of the ATP-sensitive K+ (K-ATP) channel have been examined in rabbit ventricular myocytes, using the patch-clamp technique. The sulfhydryl oxidizing agent 5.5'-dithio-bis-(2-nitro-benzoic acid) (DTNB) induced an inhibition of the channel activity without change in the single channel conductance. DTNB had no effect on the inhibitory action by ATP. Analysis of the open and closed time distributions showed that DTNB decreased the life time of bursts and increased the interburst interval without changes in open and closed time distributions shorter than 5 ms. N-ethylmaleimide (NEM), a substance that reacts with sulfhydryl groups of cysteine residues in proteins, induced an irreversible closure of the channel. The results suggested that changes in the sulfhydryl redox also modulate K-ATP channel activity of the K-ATP channel in rabbit ventricular myocytes. (C) 1996 Academic Press, Inc.
引用
收藏
页码:900 / 903
页数:4
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