Role of glutamatergic and GABAergic systems in alcoholism

被引:59
作者
Davis, KM
Wu, JY
机构
[1] Univ Kansas, Dept Mol Biosci, Lawrence, KS 66045 USA
[2] Univ Kansas, Dept Med Chem, Lawrence, KS 66045 USA
关键词
L-glutamate; GABA; alcoholism; glutamate receptors; GABA receptors; decarboxylase;
D O I
10.1159/000054008
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The pharmacological effects of ethanol are complex and widespread without a well-defined target. Since glutamatergic and GABAergic innervation a re both dense a nd diffuse and account for more than 80% of the neuronal circuitry in the human brain, alterations in glutamatergic and GABAergic function could affect the function of all neurotransmitter systems. Here, we review recent progress in glutamatergic and GABAergic systems with a special focus on their roles in alcohol dependence and alcohol withdrawal-induced seizures. In particular, NMDA-receptors appear to play a central role in alcohol dependence and alcohol-induced neurological disorders. Hence, NMDA receptor antagonists may have multiple functions in treating alcoholism and other addictions and they may become important therapeutics for numerous disorders including epilepsy, Parkinson's disease, amyotrophic lateral sclerosis, Huntington's chorea, anxiety, neurotoxicity, ischemic stroke, and chronic pain. One of the new family of NMDA receptor antagonists, such as DETC-MESO, which regulate the redox site of NMDA receptors, may prove to be the drug of choice for treating alcoholism as well as many neurological diseases. Copyright (C) 2001 National Science Council, ROC and S. Karger AG. Basel.
引用
收藏
页码:7 / 19
页数:13
相关论文
共 234 条
[1]   Alterations of benzodiazepine receptors in type II alcoholic subjects measured with SPECT and [123I]iomazenil [J].
Abi-Dargham, A ;
Krystal, JH ;
Anjilvel, S ;
Scanley, BE ;
Zoghbi, S ;
Baldwin, RM ;
Rajeevan, N ;
Ellis, S ;
Petrakis, IL ;
Seibyl, JP ;
Charney, DS ;
Laruelle, M ;
Innis, RB .
AMERICAN JOURNAL OF PSYCHIATRY, 1998, 155 (11) :1550-1555
[2]   Ability of baclofen in reducing alcohol craving and intake: II - Preliminary clinical evidence [J].
Addolorato, G ;
Caputo, F ;
Capristo, E ;
Colombo, G ;
Gessa, GL ;
Gasbarrini, G .
ALCOHOL-CLINICAL AND EXPERIMENTAL RESEARCH, 2000, 24 (01) :67-71
[3]  
AGUAYO LG, 1994, J PHARMACOL EXP THER, V270, P61
[4]   ETHANOL-INDUCED CHANGES IN CHLORIDE FLUX ARE MEDIATED BY BOTH GABA(A) AND GABA(B) RECEPTORS [J].
ALLAN, AM ;
BURNETT, D ;
HARRIS, RA .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1991, 15 (02) :233-237
[5]   Fyn tyrosine kinase reduces the ethanol inhibition of recombinant NR1/NR2A but not NR1/NR2B NMDA receptors expressed in HEK 293 cells [J].
Anders, DL ;
Blevins, T ;
Sutton, G ;
Swope, S ;
Chandler, LJ ;
Woodward, JJ .
JOURNAL OF NEUROCHEMISTRY, 1999, 72 (04) :1389-1393
[6]   Reduced ethanol inhibition of N-methyl-D-aspartate receptors by deletion of the NR1 C0 domain or overexpression of α-actinin-2 proteins [J].
Anders, DL ;
Blevins, T ;
Smothers, CT ;
Woodward, JJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (20) :15019-15024
[7]  
ARDENT T, 1988, BRAIN RES B, V21, P563
[8]   BRAIN L-GLUTAMATE DECARBOXYLASE - INHIBITION BY PHOSPHORYLATION AND ACTIVATION BY DEPHOSPHORYLATION [J].
BAO, J ;
CHEUNG, WY ;
WU, JY .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (12) :6464-6467
[9]  
Bao Jun, 1994, Journal of Biomedical Science, V1, P237, DOI 10.1007/BF02253308
[10]   LONG-TERM POTENTIATION OF NMDA RECEPTOR-MEDIATED SYNAPTIC TRANSMISSION IN THE HIPPOCAMPUS [J].
BASHIR, ZI ;
ALFORD, S ;
DAVIES, SN ;
RANDALL, AD ;
COLLINGRIDGE, GL .
NATURE, 1991, 349 (6305) :156-158