Genetic determinants of severity of acute withdrawal from diazepam in mice: Commonality with ethanol and pentobarbital

被引:20
作者
Metten, P
Crabbe, JC
机构
[1] VAMC, Res Serv, Portland, OR 97201 USA
[2] Oregon Hlth Sci Univ, Dept Behav Neurosci, Portland Alcohol Res Ctr, Portland, OR 97201 USA
关键词
benzodiazepines; diazepam; ethanol; flumazenil; genetic correlation; genetic determinants; handling-induced convulsions; inbred strains; mouse; pentobarbital; pharmacogenetics; withdrawal;
D O I
10.1016/S0091-3057(99)00017-9
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Potentially life-threatening seizures can occur following withdrawal from benzodiazepines, ethanol, or barbiturates. In animals, withdrawal severity has been shown to be partially genetically determined for each drug class. Susceptibility to these drugs is partially determined by common genetic factors, but the evidence is conflicting. We tested the hypothesis that acute benzodiazepine withdrawal convulsions are influenced by at least some genes that also affect withdrawal from ethanol and pentobarbital. Results in inbred mouse strains demonstrate that strain susceptibility is genetically correlated with susceptibility to ethanol and pentobarbital. The proportion of variance accounted for by genetic factors common to diazepam and ethanol was estimated at 69%. Results contrast with previous data obtained in mice that were serially tested for withdrawal severity from ethanol, pentobarbital, and then diazepam, because serial testing of mice significantly affected the previous results for some strains. Diazepam withdrawal severity was also genetically correlated with pentobarbital withdrawal. Together, these results suggest that some genes influence severity of withdrawal from several types of depressant drugs. (C) 1999 Elsevier Science Inc.
引用
收藏
页码:473 / 479
页数:7
相关论文
共 56 条
[1]   Exacerbation of ethanol withdrawal seizures in mice with a history of multiple withdrawal experience [J].
Becker, HC ;
DiazGranados, JL ;
Hale, RL .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1997, 57 (1-2) :179-183
[2]   POSITIVE RELATIONSHIP BETWEEN THE NUMBER OF PRIOR ETHANOL WITHDRAWAL EPISODES AND THE SEVERITY OF SUBSEQUENT WITHDRAWAL SEIZURES [J].
BECKER, HC .
PSYCHOPHARMACOLOGY, 1994, 116 (01) :26-32
[3]   BARBITURATE DEPENDENCE IN MICE - EFFECTS OF CONTINUOUS VS DISCONTINUOUS DRUG ADMINISTRATION [J].
BELKNAP, JK ;
ONDRUSEK, G ;
BERG, J ;
WADDINGHAM, S .
PSYCHOPHARMACOLOGY, 1977, 51 (02) :195-198
[4]   ETHANOL AND DIAZEPAM WITHDRAWAL CONVULSIONS ARE EXTENSIVELY CODETERMINED IN WSP AND WSR MICE [J].
BELKNAP, JK ;
CRABBE, JC ;
LAURSEN, SE .
LIFE SCIENCES, 1989, 44 (26) :2075-2080
[5]   ETHANOL AND NITROUS-OXIDE PRODUCE WITHDRAWAL-INDUCED CONVULSIONS BY SIMILAR MECHANISMS IN MICE [J].
BELKNAP, JK ;
LAURSEN, SE ;
CRABBE, JC .
LIFE SCIENCES, 1987, 41 (17) :2033-2040
[6]   ETHANOL AND BARBITURATE WITHDRAWAL CONVULSIONS ARE EXTENSIVELY CODETERMINED IN MICE [J].
BELKNAP, JK ;
DANIELSON, PW ;
LAME, M ;
CRABBE, JC .
ALCOHOL, 1988, 5 (02) :167-171
[7]  
BELKNAP JK, 1980, ALCOHOL TOLERANCE DE, P157
[8]  
BUCK KJ, 1991, J PHARMACOL EXP THER, V257, P984
[9]  
Buck KJ, 1997, J NEUROSCI, V17, P3946
[10]   Molecular genetic analysis of the role of GABAergic systems in the behavioral and cellular actions of alcohol [J].
Buck, KJ .
BEHAVIOR GENETICS, 1996, 26 (03) :313-323