Neuronal nicotinic acetylcholine receptor modulation by general anesthetics

被引:34
作者
Flood, P [1 ]
Role, LW [1 ]
机构
[1] Columbia Univ, Dept Anesthesiol, New York, NY 10032 USA
关键词
general anesthetics; neuronal nicotinic acetylcholine receptors; inhibition;
D O I
10.1016/S0378-4274(98)00179-9
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
1. General anesthetics-have been shown to inhibit synaptic transmission in multiple areas of the central and peripheral nervous systems. 2. The mechanism of inhibition is not well understood. 3. It has become clear that general anesthetics modulate the function of members of the ligand gated ion channel superfamily, including receptors for GABA(A), glycine (Harrison et al., Mol. Pharmacol. 44(3), 1993, 628-632) and 5HT(3) (Zhou and Lovinger, J. Pharmacol. Exp. Therap. 278(2), 1996, 732-740). 4. Studies of the activity of general anesthetics on recombinant neuronal nicotinic acetylcholine receptors have added this receptor family to those potently inhibited by general anesthetics (Flood et al., Anesthesiology 86(4), 1997, 859-865; Violet et al., Anesthesiology 86(4), 1997, 866-874). 5. Studies of neuronal nicotinic receptors in native neurons suggest that the inhibition of these receptors by general anesthetics at low clinical concentrations may be biologically significant (Nicoll, Science 199(4327), 1978, 451-452). 6. Recent work on neuronal nicotinic acetylcholine receptors in the central nervous system suggests that their primary role may be to modulate synaptic transmission (Role and Berg, Neuron 16(6), 1996, 1077-1085). 7. Thus, inhibition of nicotinic modulation in the central nervous system may result in inhibition of synaptic transmission and some of the behavioral consequences of general anesthesia. (C) 1998 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:149 / 153
页数:5
相关论文
共 26 条
[1]  
ANAND RC, 1995, J BIOL CHEM, V266, P11192
[2]   ANESTHETIC MODULATION OF NICOTINIC ION-CHANNEL KINETICS IN BOVINE CHROMAFFIN CELLS [J].
CHARLESWORTH, P ;
RICHARDS, CD .
BRITISH JOURNAL OF PHARMACOLOGY, 1995, 114 (04) :909-917
[3]   THE ALPHA-5-GENE PRODUCT ASSEMBLES WITH MULTIPLE ACETYLCHOLINE-RECEPTOR SUBUNITS TO FORM DISTINCTIVE RECEPTOR SUBTYPES IN BRAIN [J].
CONROY, WG ;
VERNALLIS, AB ;
BERG, DK .
NEURON, 1992, 9 (04) :679-691
[4]   PENTAMERIC STRUCTURE AND SUBUNIT STOICHIOMETRY OF A NEURONAL NICOTINIC ACETYLCHOLINE-RECEPTOR [J].
COOPER, E ;
COUTURIER, S ;
BALLIVET, M .
NATURE, 1991, 350 (6315) :235-238
[5]  
DILGER JP, 1993, MOL PHARMACOL, V44, P1056
[6]   ACTIONS OF GENERAL-ANESTHETICS ON ACETYLCHOLINE RECEPTOR-RICH MEMBRANES FROM TORPEDO-CALIFORNICA [J].
FIRESTONE, LL ;
SAUTER, JF ;
BRASWELL, LM ;
MILLER, KW .
ANESTHESIOLOGY, 1986, 64 (06) :694-702
[7]   alpha 4 beta 2 neuronal nicotinic acetylcholine receptors in the central nervous system are inhibited by isoflurane and propofol, but alpha 7-type nicotinic acetylcholine receptors are unaffected [J].
Flood, P ;
RamirezLatorre, J ;
Role, L .
ANESTHESIOLOGY, 1997, 86 (04) :859-865
[8]  
FORMAN SA, 1995, MOL PHARMACOL, V48, P574
[9]   STEREOSPECIFIC EFFECTS OF INHALATIONAL GENERAL ANESTHETIC OPTICAL ISOMERS ON NERVE ION CHANNELS [J].
FRANKS, NP ;
LIEB, WR .
SCIENCE, 1991, 254 (5030) :427-430
[10]   Hippocampal synaptic transmission enhanced by low concentrations of nicotine [J].
Gray, R ;
Rajan, AS ;
Radcliffe, KA ;
Yakehiro, M ;
Dani, JA .
NATURE, 1996, 383 (6602) :713-716