Beeler T, Gable K
Department of Biochemistry, Uniformed Services University of the Health Sciences, Bethesda, MD 20014.
FEBS Lett. 1993 Oct 4;331(3):207-10. doi: 10.1016/0014-5793(93)80338-u.
The effect of the general anesthetic halothane on the activity of the rat skeletal muscle Ca(2+)-activated K+ channel in planar lipid bilayers was investigated. Halothane concentrations in the clinical range (1.0-0.2 mM) alter the regulation of the channel by both Ca2+ and membrane potential. At Ca2+ concentrations between 10 and 250 microM and membrane potentials between 0 and -30 mV, halothane significantly decreases the open state probability without changing the channel conductance. The results demonstrate that halothane can act directly on the Ca(2+)-activated K+ channel or its lipid environment to alter the channel gating kinetics.
研究了全身麻醉药氟烷对平面脂质双分子层中大鼠骨骼肌钙激活钾通道活性的影响。临床范围内的氟烷浓度(1.0 - 0.2 mM)会改变通道受钙离子和膜电位的调节。在钙离子浓度为10至250微摩尔/升以及膜电位为0至 -30毫伏之间时,氟烷显著降低开放态概率,而不改变通道电导。结果表明,氟烷可直接作用于钙激活钾通道或其脂质环境,以改变通道门控动力学。