VOLATILE ANESTHETICS SELECTIVELY ALTER [H-3] RYANODINE BINDING TO SKELETAL AND CARDIAC RYANODINE RECEPTORS

被引:32
作者
CONNELLY, TJ [1 ]
ELHAYEK, R [1 ]
RUSY, BF [1 ]
CORONADO, R [1 ]
机构
[1] UNIV WISCONSIN,DEPT PHYSIOL,MADISON,WI 53792
关键词
D O I
10.1016/S0006-291X(05)80850-2
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 effect of clinical concentrations of volatile anesthetics on ryanodine receptors of cardiac and skeletal muscle sarcoplasmic reticulum was evaluated using [3H]ryanodine binding. At 2 volume percent, halothane and enflurane stimulated binding to cardiac SR by 238% and 204%, respectively, while isoflurane had no effect. In contrast, halothane and enflurane had no effect on [3H]ryanodine binding to skeletal ryanodine receptors, while isoflurane produced a significant stimulation. These results suggest that volatile anesthetics interact in a site-specific manner with ryanodine receptors of cardiac or skeletal muscle to effect Ca2+ release-channel gating. © 1992 Academic Press, Inc.
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页码:595 / 600
页数:6
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