Isoflurane antagonizes the capacity of flurothyl or 1,2-dichlorohexafluorocyclobutane to impair fear conditioning to context and tone

被引:12
作者
Eger, EI
Xing, YL
Pearce, R
Shafer, S
Laster, MJ
Zhang, Y
Fanselow, MS
Sonner, JM
机构
[1] Univ Calif San Francisco, Dept Anesthesia & Perioperat Care, San Francisco, CA 94143 USA
[2] Univ Wisconsin, Dept Anesthesiol, Madison, WI USA
[3] Stanford Univ, Dept Anesthesiol, Stanford, CA 94305 USA
[4] Univ Calif Los Angeles, Dept Psychol, Los Angeles, CA 90024 USA
关键词
D O I
10.1213/01.ANE.0000055360.30078.FF
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
In animals, the conventional inhaled anesthetic, isoflurane, impairs learning fear to context and fear to tone, doing so at concentrations that produce amnesia in humans. Nonimmobilizers are inhaled compounds that do not produce immobility in response to noxious stimulation, nor do they decrease the requirement for conventional inhaled anesthetics. Like isoflurane, the nonimmobilizer 1,2-dichlorohexafluorocyclobutane (2N) impairs learning at concentrations less than those predicted from its lipophilicity to produce anesthesia. The capacity of the nonimmobilizer di-(2,2,2,trifluoroethyl) ether (flurothyl) to affect learning and memory has not been studied. Both nonimmobilizers can cause convulsions. We hypothesized that if isoflurane, 2N, and flurothyl act by the same mechanism to impair learning and memory, their effects should be additive. We found that isoflurane, 2N, and flurothyl (each, alone) impaired learning fear to context and fear to tone in rats, with the nonimmobilizers doing so at concentrations less than those that cause convulsions. (Fear was defined by freezing [volitional immobility] in the presence of the conditioned stimulus [context or tone].) However, the combination of isoflurane and 2N or flurothyl produced an antagonistic rather than an additive effect on learning, a finding in conflict with our hypothesis. And flurothyl was no less potent than 2N (at least no less potent relative to the concentration of each that produced convulsions) in its capacity to impair learning. We conclude that conventional inhaled anesthetics and nonimmobilizers impair learning and memory by different mechanisms. The basis for this impairment remains unknown.
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页码:1010 / 1018
页数:9
相关论文
共 29 条
[1]   Inhaled nonimmobilizers do not alter the middle latency auditory-evoked response of rats [J].
Dutton, RC ;
Rampil, IJ ;
Eger, EI .
ANESTHESIA AND ANALGESIA, 2000, 90 (01) :213-217
[2]   Nonimmobilizers and transitional compounds may produce convulsions by two mechanisms [J].
Eger, EI ;
Koblin, DD ;
Sonner, J ;
Gong, D ;
Laster, MJ ;
Ionescu, P ;
Halsey, MJ ;
Hudlicky, T .
ANESTHESIA AND ANALGESIA, 1999, 88 (04) :884-892
[3]   Hypothesis: Inhaled anesthetics produce immobility and amnesia by different mechanisms at different sites [J].
Eger, EI ;
Koblin, DD ;
Harris, RA ;
Kendig, JJ ;
Pohorille, A ;
Halsey, MJ ;
Trudell, JR .
ANESTHESIA AND ANALGESIA, 1997, 84 (04) :915-918
[4]   Convulsant activity of nonanesthetic gas combinations [J].
Fang, ZX ;
Laster, MJ ;
Gong, D ;
Ionescu, P ;
Koblin, DD ;
Sonner, J ;
Eger, EI ;
Halsey, MJ .
ANESTHESIA AND ANALGESIA, 1997, 84 (03) :634-640
[5]  
FANSELOW MS, 1980, PAVLOVIAN J BIOL SCI, V15, P177
[6]   Why we think plasticity underlying pavlovian fear conditioning occurs in the basolateral amygdala [J].
Fanselow, MS ;
LeDoux, JE .
NEURON, 1999, 23 (02) :229-232
[7]   The neuroanatomical and neurochemical basis of conditioned fear [J].
Fendt, M ;
Fanselow, MS .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 1999, 23 (05) :743-760
[8]   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
[9]   Nonanesthetics can suppress learning [J].
Kandel, L ;
Chortkoff, BS ;
Sonner, J ;
Laster, MJ ;
Eger, EI .
ANESTHESIA AND ANALGESIA, 1996, 82 (02) :321-326
[10]   MODALITY-SPECIFIC RETROGRADE-AMNESIA OF FEAR [J].
KIM, JJ ;
FANSELOW, MS .
SCIENCE, 1992, 256 (5057) :675-677