State-dependent mibefradil block of Na+ channels

被引:51
作者
McNulty, MM
Hanck, DA
机构
[1] Univ Chicago, Dept Neurobiol Pharmacol & Physiol, Chicago, IL 60637 USA
[2] Univ Chicago, Dept Med, Chicago, IL 60637 USA
关键词
D O I
10.1124/mol.66.6.1652
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Mibefradil is a T-type Ca2+ channel antagonist with reported cross-reactivity with other classes of ion channels, including K+, Cl-, and Na+ channels. Using whole-cell voltage clamp, we examined mibefradil block of four Na+ channel isoforms expressed in human embryonic kidney cells: Na(v)1.5 (cardiac), Na(v)1.4 (skeletal muscle), Na(v)1.2 (brain), and Na(v)1.7 (peripheral nerve). Mibefradil blocked Na(v)1.5 in a use/frequency-dependent manner, indicating preferential binding to states visited during depolarization. Mibefradil blocked currents of all Na+ channel isoforms with similar affinity and a dependence on holding potential, and drug off-rate was slowed at depolarized potentials ( k(off) was 0.024/s at - 130 mV and 0.007/ s at - 100 mV for Na-v 1.5). We further probed the interaction of mibefradil with inactivated Na(v)1.5 channels. Neither the degree nor the time course of block was dependent on the stimulus duration, which dramatically changed the residency time of channels in the fast-inactivated state. In addition, inhibiting the binding of the fast inactivation lid (Na-v 1.5 ICM + MTSET) did not alter mibefradil block, confirming that the drug does not preferentially interact with the fast-inactivated state. We also tested whether mibefradil interacted with slow-inactivated state(s). When selectively applied to channels after inducing slow inactivation with a 60-s pulse to - 10 mV, mibefradil (1 muM) produced 45% fractional block in Na-v 1.5 and greater block (88%) in an isoform (Na-v 1.4) that slow-inactivates more completely. Our results suggest that mibefradil blocks Na+ channels in a state-dependent manner that does not depend on fast inactivation but probably involves interaction with one or more slow-inactivated state(s).
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页码:1652 / 1661
页数:10
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