Rapid and chronic: Two distinct forms of ethanol tolerance in Drosophila

被引:62
作者
Berger, KH
Heberlein, U
Moore, MS
机构
[1] Ernest Gallo Clin & Res Ctr, Emeryville, CA 94608 USA
[2] Univ Calif San Francisco, Dept Anat, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Neurosci Program, San Francisco, CA 94143 USA
关键词
Drosophila; ethanol; intoxication; tolerance; chronic exposure;
D O I
10.1097/01.ALC.0000141817.15993.98
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
Background: Ethanol tolerance, defined as a reduction in the intensity of the effects of ethanol upon continuous or repeated exposure, is a hallmark of alcoholism. Tolerance may develop at the cellular or neural systems levels. The molecular changes underlying ethanol tolerance are not well understood. We therefore explored the utility of Drosophila, with its accessibility to genetic, molecular, and behavioral analyses, as a model organism to study tolerance development in response to different ethanol-exposure regimens. Methods: We describe a new assay that quantifies recovery from ethanol intoxication in Drosophila. Using this recovery assay, we define ethanol pre-exposure paradigms that lead to the development of tolerance. We also use the inebriometer, an assay that measures the onset of intoxication, to study the effects of pharmacological and genetic manipulations on tolerance development. Results: We show that flies develop different forms of ethanol tolerance: rapid tolerance, induced by a single short exposure to a high concentration of ethanol, and chronic tolerance, elicited by prolonged exposure to a low concentration of the drug. Neither rapid nor chronic tolerance involves changes in ethanol pharmacokinetics, implying that they represent functional rather than dispositional tolerance. Chronic and rapid tolerance can be distinguished mechanistically: chronic tolerance is disrupted by treatment with the protein synthesis inhibitor cycloheximide, whereas rapid tolerance is resistant to this treatment. Furthermore, rapid and chronic tolerance rely on distinct genetic pathways: a mutant defective for octopamine biosynthesis shows reduced rapid tolerance but normal chronic tolerance. Conclusions: Flies, like mammals, develop tolerance in response to different ethanol-exposure regimens, and this tolerance affects both the onset of and the recovery from acute intoxication. Two forms of tolerance, rapid and chronic, are mechanistically distinct, because they can be dissociated genetically and pharmacologically.
引用
收藏
页码:1469 / 1480
页数:12
相关论文
共 37 条
[1]   Sensitivity to ethanol-induced motor incoordination in 5-HT1B receptor null mutant mice is task-dependent:: Implications for behavioral assessment of genetically altered mice [J].
Boehm, SL ;
Schafer, GL ;
Phillips, TJ ;
Browman, KE ;
Crabbe, JC .
BEHAVIORAL NEUROSCIENCE, 2000, 114 (02) :401-409
[2]   EFFECT OF RAPHE LESIONS ON THE DEVELOPMENT OF ACUTE TOLERANCE TO ETHANOL AND PENTOBARBITAL [J].
CAMPANELLI, C ;
LE, AD ;
KHANNA, JM ;
KALANT, H .
PSYCHOPHARMACOLOGY, 1988, 96 (04) :454-457
[3]  
COHAN FM, 1986, GENETICS, V114, P145
[4]  
CRABBE JC, 1979, J PHARMACOL EXP THER, V208, P128
[5]   Genotypic differences in ethanol sensitivity in two tests of motor incoordination [J].
Crabbe, JC ;
Metten, P ;
Yu, CH ;
Schlumbohm, JP ;
Cameron, AJ ;
Wahlsten, D .
JOURNAL OF APPLIED PHYSIOLOGY, 2003, 95 (04) :1338-1351
[6]   GENETIC ANIMAL-MODELS OF ALCOHOL AND DRUG-ABUSE [J].
CRABBE, JC ;
BELKNAP, JK ;
BUCK, KJ .
SCIENCE, 1994, 264 (5166) :1715-1723
[7]   Phenotypic and genotypic relationships between ethanol tolerance and sensitivity in mice selectively bred for initial sensitivity to ethanol (SS and LS) or development of acute tolerance (HAFT and LAFT) [J].
Deitrich, RA ;
Bludeau, P ;
Erwin, VG .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 2000, 24 (05) :595-604
[8]   γ-aminobutyric acid B receptor 1 mediates behavior-impairing actions of alcohol in Drosophila:: Adult RNA interference and pharmacological evidence [J].
Dzitoyeva, S ;
Dimitrijevic, N ;
Manev, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (09) :5485-5490
[9]   Effects of moderate alcohol consumption on the central nervous system [J].
Eckardt, MJ ;
File, SE ;
Gessa, GL ;
Grant, KA ;
Guerri, C ;
Hoffman, PL ;
Kalant, H ;
Koob, GF ;
Li, TK ;
Tabakoff, B .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1998, 22 (05) :998-1040
[10]  
Erwin VG, 1996, J PHARMACOL EXP THER, V279, P1310