Convulsant activity of nonanesthetic gas combinations

被引:18
作者
Fang, ZX
Laster, MJ
Gong, D
Ionescu, P
Koblin, DD
Sonner, J
Eger, EI
Halsey, MJ
机构
[1] UNIV CALIF SAN FRANCISCO,DEPT ANESTHESIA,SAN FRANCISCO,CA 94143
[2] NUFFIELD DEPT ANAESTHET,OXFORD,ENGLAND
关键词
D O I
10.1097/00000539-199703000-00032
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Most nonanesthetics (inhaled compounds that neither cause anesthesia when given alone nor decrease the partial pressure of a known inhaled anesthetic required to produce anesthesia) and transitional compounds (inhaled compounds that are less potent than would be predicted by the Meyer-Overton hypothesis) cause convulsions. A possible exception is the perfluoroalkane series of nonanesthetics. The present study tested whether perfluoroalkanes do provide an exception. Further, we tested whether the convulsant effects of nonanesthetic and transitional compounds were additive. The nonanesthetic perfluoropropane caused convulsions at 7.5 +/- 0.7 atm (mean +/- SD). Convulsions also were produced by perfluorocyclobutane (0.976 +/- 0.002 atm), 1,2-dichlorotetrafluoroethane (0.358 +/- 0.011 atm), 2,3-dichlorooctafluorobutane (0.085 +/- 0.007 atm), 1,2-dichlorohexafluorocyclobutane (0.055 +/- 0.007 atm), and flurothyl (0.00156 +/- 0.00039 atm). Of these, 1,2-dichlorotetrafluoroethane is a transitional compound, the remainder being nonanesthetics. The combination of flurothyl plus 1,2-dichlorohexafluorocyclobutane gave evidence of antagonism (a 17% +/- 21% deviation from additivity; P < 0.05), whereas the combination of 1,2-dichlorotetrafluoroethane plus 2,3-dichlorooctafluorobutane gave evidence of synergy (a -13% +/- 8% deviation from additivity; P < 0.05). The combinations of perfluoropropane plus perfluorocyclobutane (-4% +/- 15%), and perfluoropropane plus 1,2-dichlorohexafluorocyclobutane (-1% +/- 26%) did not produce results that deviated significantly from additivity. We conclude that pairs of these compounds either produce convulsions in an additive manner, a finding consistent with (but not proving) a common mode of action; or deviate modestly from additivity, a finding suggesting that at least a portion of the mechanistic basis for convulsions might differ, particularly for flurothyl plus other nonanesthetics, or for the combination of nonanesthetics and transitional compounds.
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页码:634 / 640
页数:7
相关论文
共 18 条
[1]   REGIONAL RAT-BRAIN BENZODIAZEPINE RECEPTOR NUMBER AND GAMMA-AMINOBUTYRIC ACID CONCENTRATION FOLLOWING A CONVULSION [J].
BOWDLER, JM ;
GREEN, AR .
BRITISH JOURNAL OF PHARMACOLOGY, 1982, 76 (02) :291-298
[2]  
COLE DJ, 1990, ANESTH ANALG, V70, P126
[3]  
EGER EI, 1987, ANESTH ANALG, V66, P971
[4]  
EGER EI, 1994, ANESTH ANALG, V79, P245
[5]   Anesthetic and convulsant properties of aromatic compounds and cycloalkanes: Implications for mechanisms of narcosis [J].
Fang, ZX ;
Sonner, J ;
Laster, MJ ;
Ionescu, P ;
Kandel, L ;
Koblin, DD ;
Eger, EI ;
Halsey, MJ .
ANESTHESIA AND ANALGESIA, 1996, 83 (05) :1097-1104
[6]  
GONSOWSKI CT, 1994, ANESTH ANALG, V79, P710
[7]   ELECTROENCEPHALOGRAPHIC SEIZURE ACTIVITY IN DOGS DURING ANAESTHESIA - STUDIES WITH ETHRANE, FLUROXENE, HALOTHANE, CHLOROFORM, DIVINYL ETHER, DIETHYL ETHER, METHOXYFLURANE, CYCLOPROPANE AND FORANE [J].
JOAS, TA ;
STEVENS, WC ;
EGER, EI .
BRITISH JOURNAL OF ANAESTHESIA, 1971, 43 (08) :739-+
[8]  
KOBLIN DD, 1981, ANESTH ANALG, V60, P464
[9]  
KOBLIN DD, 1994, ANESTH ANALG, V79, P1043
[10]  
KRANTZ JC, 1967, ANESTH ANAL CURR RES, V46, P271