Strain differences in the antinociceptive effect of nitrous oxide on the tail flick test in rats

被引:26
作者
Fender, C
Fujinaga, M
Maze, M
机构
[1] Univ London Imperial Coll Sci Technol & Med, Sch Med, Magill Dept Anaesthet, London SW10 9NH, England
[2] Stanford Univ, Sch Med, Dept Anesthesia, Stanford, CA 94305 USA
[3] Vet Adm Palo Alto Hlth Care Syst, Anesthesiol Serv, Palo Alto, CA USA
关键词
D O I
10.1097/00000539-200001000-00039
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
To study strain differences in antinociceptive effects of nitrous oxide (N2O), we examined various outbred and inbred stains of rats by using tail flick latency response. All outbred strains, i.e., Sprague-Dawley from two different breeders, Wistar, and Long-Evans, showed a similar antinociceptive response. Namely, the peak response occurred after 30 min of exposure, and tolerance to N2O developed within 60 to 90 min. Each of the four inbred stains examined, i.e., Wistar-Kyoto, Brown-Norway, Fischer, and Lewis, displayed a unique pattern of antinociceptive response to N2O. Wistar-Kyoto and Brown-Norway strains showed somewhat similar patterns as those observed in outbred strains, apart from the fact that the Wistar-Kyoto displayed a more distinct development of tolerance, whereas, the Brown-Norway strain had a lower peak effect. The Fischer strain displayed the greatest antinociceptive response to N2O, and did not develop tolerance. The Lewis strain showed no antinociceptive response to N2O. These results indicate differences in the durability and the magnitude of the antinociceptive response to N2O among various strains of rats. Implications: Because of the variability that already exists, we recommend that animal studies examining the antinociceptive effects of nitrous oxide should be performed on inbred rat strains.
引用
收藏
页码:195 / 199
页数:5
相关论文
共 21 条
[1]   DOPAMINERGIC BRAIN REWARD REGIONS OF LEWIS AND FISCHER RATS DISPLAY DIFFERENT LEVELS OF TYROSINE-HYDROXYLASE AND OTHER MORPHINE-REGULATED AND COCAINE-REGULATED PHOSPHOPROTEINS [J].
BEITNERJOHNSON, D ;
GUITART, X ;
NESTLER, EJ .
BRAIN RESEARCH, 1991, 561 (01) :147-150
[2]   TOLERANCE TO NITROUS-OXIDE ANALGESIA IN RATS AND MICE [J].
BERKOWITZ, BA ;
FINCK, AD ;
HYNES, MD ;
NGAI, SH .
ANESTHESIOLOGY, 1979, 51 (04) :309-312
[3]  
BERKOWITZ BA, 1977, J PHARMACOL EXP THER, V203, P539
[4]   Opiate receptors in the periaqueductal gray mediate analgesic effect of nitrous oxide in rats [J].
Fang, F ;
Guo, TZ ;
Davies, MF ;
Maze, M .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1997, 336 (2-3) :137-141
[5]   FISCHER AND LEWIS RAT STRAINS DIFFER IN BASAL LEVELS OF NEUROFILAMENT PROTEINS AND THEIR REGULATION BY CHRONIC MORPHINE IN THE MESOLIMBIC DOPAMINE SYSTEM [J].
GUITART, X ;
BEITNERJOHNSON, D ;
MARBY, DW ;
KOSTEN, TA ;
NESTLER, EJ .
SYNAPSE, 1992, 12 (03) :242-253
[6]   LEWIS AND FISCHER RAT STRAINS DISPLAY DIFFERENCES IN BIOCHEMICAL, ELECTROPHYSIOLOGICAL AND BEHAVIORAL PARAMETERS - STUDIES IN THE NUCLEUS-ACCUMBENS AND LOCUS-CERULEUS OF DRUG NAIVE AND MORPHINE-TREATED ANIMALS [J].
GUITART, X ;
KOGAN, JH ;
BERHOW, M ;
TERWILLIGER, RZ ;
AGHAJANIAN, GK ;
NESTLER, EJ .
BRAIN RESEARCH, 1993, 611 (01) :7-17
[7]   Antinociceptive response to nitrous oxide is mediated by supraspinal opiate and spinal alpha(2) adrenergic receptors in the rat [J].
Guo, TZ ;
Poree, L ;
Golden, W ;
Stein, J ;
Fujinaga, M ;
Maze, M .
ANESTHESIOLOGY, 1996, 85 (04) :846-852
[8]   Nitrous oxide produces antinociceptive response via α2B and/or α2C adrenoceptor subtypes in mice [J].
Guo, TZ ;
Davies, MF ;
Kingery, WS ;
Patterson, AJ ;
Limbird, LE ;
Maze, M .
ANESTHESIOLOGY, 1999, 90 (02) :470-476
[9]  
HAMMOND DL, 1989, ADV PAIN RES THER, V12, P69
[10]  
LI TK, 1984, ALCOHOL CLIN EXP RES, V8, P485