Volatile anesthetics significantly suppress central and peripheral mammalian sodium channels

被引:20
作者
Duch, DS
Rehberg, B
Vysotskaya, TN
机构
[1] Cornell Univ, Coll Med, Dept Anesthesiol, New York, NY 10021 USA
[2] Cornell Univ, Coll Med, Dept Physiol, New York, NY 10021 USA
关键词
mammalian sodium channels; volatile anesthetics; suppress;
D O I
10.1016/S0378-4274(98)00193-3
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
1. Voltage-dependent sodium channels are important for neuronal signal propagation and integration. 2. Non-mammalian preparations, such as squid giant axon, have sodium channels which have been found to be insensitive to clinical anesthetic concentrations. 3. On the other hand, sodium channels from mammalian neurons are much more sensitive to block by volatile anesthetics. 4. Due to a significant hyperpolarizing shift in steady-slate inactivation, IC(50)s for sodium channel block at potentials close to the resting membrane potential overlapped with clinical anesthetic concentrations. 5. Hence, sodium channels in mammalian neurons may be sensitive molecular targets of volatile anesthetics. (C) 1998 Published by Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:255 / 263
页数:9
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