Insulin modulation of ATP-sensitive K+ channel of rat skeletal muscle is impaired in the hypokalaemic state

被引:16
作者
Tricarico, D
Capriulo, R
Camerino, DC
机构
[1] Univ Bari, Fac Pharm, Dept Pharmacobiol, Pharmacol Unit, I-70126 Bari, Italy
[2] Univ Bari, Fac Med, Clin Anaesthesiol & Intens Care, Bari, Italy
来源
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY | 1999年 / 437卷 / 02期
关键词
hypokalaemic periodic paralysis; ATP-sensitive K+ channels; insulin; skeletal muscle; patch clamp;
D O I
10.1007/s004240050774
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
In the present work, we examined the effects of in vivo administration of insulin to rats made hypokalaemic by feeding a K+-free diet. The i.p. injection of insulin in the hypokalaemic rats provoked muscle paralysis within 3-5 h. Consistent with this observation, the skeletal muscle fibres of the paralysed rats were depolarized. In contrast, in the normokalaemic animals, insulin neither provoked paralysis nor produced significant fibre hyperpolarization. In the hypokalaemic rats, insulin almost completely abolished the sarcolemma adenosine triphosphate (ATP)-sensitive K+ currents without altering the sensitivity of the channels to ATP or glibenclamide. In contrast, in the normokalaemic rats, insulin enhanced ATP-sensitive K+ currents that became also resistant to ATP and glibenclamide. Our experiments indicate that the modulation of the sarcolemma ATP-sensitive K+ channels by insulin is impaired in the hypokalaemic state. This phenomenon appears to be related to the fibre depolarization and paralysis observed in the same animals.
引用
收藏
页码:235 / 240
页数:6
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