Invertebrate models of drug abuse

被引:139
作者
Wolf, FW
Heberlein, U
机构
[1] Univ Calif San Francisco, Dept Anat, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Program Neurosci, San Francisco, CA 94143 USA
来源
JOURNAL OF NEUROBIOLOGY | 2003年 / 54卷 / 01期
关键词
invertebrates; drug abuse; drug models;
D O I
10.1002/neu.10166
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Susceptibility to drug addiction depends on genetic and environmental factors and their complex interactions. Studies with mammalian models have identified molecular targets, neurochemical systems, and brain regions that mediate some of the addictive properties of abused drugs. Yet, our understanding of how the primary effects of drugs lead to addiction remains incomplete. Recently, researchers have turned to the invertebrate model systems Drosophila melanogaster and Caenorhabditis elegans to dissect the mechanisms by which abused drugs modulate behavior. Due to their sophisticated genetics, relatively simple anatomy, and their remarkable molecular similarity to mammals, these invertebrate models should provide useful insights into the mechanisms of drug action. Here we review recent behavioral and genetic studies in flies and worms on the effects of ethanol, cocaine, and nicotine, three of the most widely abused drugs in the world. (C) 2003 Wiley Periodicals, Inc.
引用
收藏
页码:161 / 178
页数:18
相关论文
共 156 条
[1]   PKC-GAMMA MUTANT MICE EXHIBIT MILD DEFICITS IN SPATIAL AND CONTEXTUAL LEARNING [J].
ABELIOVICH, A ;
PAYLOR, R ;
CHEN, C ;
KIM, JJ ;
WEHNER, JM ;
TONEGAWA, S .
CELL, 1993, 75 (07) :1263-1271
[2]   The genome sequence of Drosophila melanogaster [J].
Adams, MD ;
Celniker, SE ;
Holt, RA ;
Evans, CA ;
Gocayne, JD ;
Amanatides, PG ;
Scherer, SE ;
Li, PW ;
Hoskins, RA ;
Galle, RF ;
George, RA ;
Lewis, SE ;
Richards, S ;
Ashburner, M ;
Henderson, SN ;
Sutton, GG ;
Wortman, JR ;
Yandell, MD ;
Zhang, Q ;
Chen, LX ;
Brandon, RC ;
Rogers, YHC ;
Blazej, RG ;
Champe, M ;
Pfeiffer, BD ;
Wan, KH ;
Doyle, C ;
Baxter, EG ;
Helt, G ;
Nelson, CR ;
Miklos, GLG ;
Abril, JF ;
Agbayani, A ;
An, HJ ;
Andrews-Pfannkoch, C ;
Baldwin, D ;
Ballew, RM ;
Basu, A ;
Baxendale, J ;
Bayraktaroglu, L ;
Beasley, EM ;
Beeson, KY ;
Benos, PV ;
Berman, BP ;
Bhandari, D ;
Bolshakov, S ;
Borkova, D ;
Botchan, MR ;
Bouck, J ;
Brokstein, P .
SCIENCE, 2000, 287 (5461) :2185-2195
[3]   Neurotransmitter transporters as molecular targets for addictive drugs [J].
Amara, SG ;
Sonders, MS .
DRUG AND ALCOHOL DEPENDENCE, 1998, 51 (1-2) :87-96
[4]   Circadian modulation of dopamine receptor responsiveness in Drosophila melanogaster [J].
Andretic, R ;
Hirsh, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (04) :1873-1878
[5]   Requirement of circadian genes for cocaine sensitization in Drosophila [J].
Andretic, R ;
Chaney, S ;
Hirsh, J .
SCIENCE, 1999, 285 (5430) :1066-1068
[6]   Dopamine modulates acute responses to cocaine, nicotine and ethanol in Drosophila [J].
Bainton, RJ ;
Tsai, LTY ;
Singh, CM ;
Moore, MS ;
Neckameyer, WS ;
Heberlein, U .
CURRENT BIOLOGY, 2000, 10 (04) :187-194
[7]   Neurobiology of the Caenorhabditis elegans genome [J].
Bargmann, CI .
SCIENCE, 1998, 282 (5396) :2028-2033
[8]   ODORANT-SELECTIVE GENES AND NEURONS MEDIATE OLFACTION IN C-ELEGANS [J].
BARGMANN, CI ;
HARTWIEG, E ;
HORVITZ, HR .
CELL, 1993, 74 (03) :515-527
[9]   High-throughput reverse genetics: RNAi screens in Caenorhabditis elegans [J].
Cornelia I Bargmann .
Genome Biology, 2 (2)
[10]   Addiction, dopamine, and the molecular mechanisms of memory [J].
Berke, JD ;
Hyman, SE .
NEURON, 2000, 25 (03) :515-532