Mood stabilizer psychopharmacology

被引:44
作者
Gould, TD [1 ]
Chen, G [1 ]
Manji, HK [1 ]
机构
[1] NIMH, Lab Mol Pathophysiol, NIH, Bethesda, MD 20892 USA
关键词
mood stabilizer; anticonvulsant; antiepileptic; neuroprotection; neurotrophic; depression; mania; ERK; bcl-2; protein kinase C; bipolar disorder; valproate;
D O I
10.1016/S1566-2772(02)00044-0
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Mood stabilizers represent a class of drugs that are efficacious in the treatment of bipolar disorder. The most established medications in this class are lithium, valproic acid, and carbamazepine. In addition to their therapeutic effects for treatment of acute manic episodes, these medications often are useful as prophylaxis against future episodes and as adjunctive antidepressant medications. While important extracellular effects have not been excluded, most available evidence suggests that the therapeutically relevant targets of this class of medications are in the interior of cells. Herein we give a prospective of a rapidly evolving field, discussing common effects of mood stabilizers as well as effects that are unique to individual medications. Mood stabilizers have been shown to modulate the activity of enzymes, ion channels, arachidonic acid turnover, G protein coupled receptors and intracellular pathways involved in synaptic plasticity and neuroprotection. Understanding the therapeutic targets of mood stabilizers will undoubtedly lead to a better understanding of the pathophysiology of bipolar disorder and to the development of improved therapeutics for the treatment of this disease. Furthermore, the involvement of mood stabilizers in pathways operative in neuroprotection suggests that they may have utility in the treatment of classical neurodegenerative disorders. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:193 / 212
页数:20
相关论文
共 250 条
[1]   DEVELOPMENT OF A NEW PHARMACOLOGICAL SEIZURE MODEL - EFFECTS OF ANTICONVULSANTS ON CORTICAL-KINDLED AND AMYGDALA-KINDLED SEIZURES IN THE RAT [J].
ALBRIGHT, PS ;
BURNHAM, WM .
EPILEPSIA, 1980, 21 (06) :681-689
[2]   REDUCED BRAIN INOSITOL IN LITHIUM-TREATED RATS [J].
ALLISON, JH ;
STEWART, MA .
NATURE-NEW BIOLOGY, 1971, 233 (43) :267-&
[3]   Comparison of fluorescence, 31P NMR, and 7Li NMR spectroscopic methods for investigating Li+/Mg2+ competition for biomolecules [J].
Amari, L ;
Layden, B ;
Rong, QF ;
Geraldes, CFGC ;
de Freitas, DM .
ANALYTICAL BIOCHEMISTRY, 1999, 272 (01) :1-7
[4]   Mechanisms of action of carbamazepine and its derivatives, oxcarbazepine, BIA 2-093, and BIA 2-024 [J].
Ambrósio, AF ;
Soares-da-Silva, P ;
Carvalho, CM ;
Carvalho, AP .
NEUROCHEMICAL RESEARCH, 2002, 27 (1-2) :121-130
[5]  
Anderson R, 2001, J MOL NEUROSCI, V16, P279
[6]  
ANLEZARK GM, 1976, BRIT J PHARMACOL, V56, pP383
[7]  
Apparsundaram S, 1998, J PHARMACOL EXP THER, V287, P733
[8]  
Apparsundaram S, 1998, J PHARMACOL EXP THER, V287, P744
[9]  
ATACK JR, 2000, BIPOLAR MED MECH ACT
[10]   CARBAMAZEPINE AND ELECTROCONVULSIVE SHOCK ATTENUATE BETA-ADRENOCEPTOR AND MUSCARINIC CHOLINOCEPTOR COUPLING TO G-PROTEINS IN RAT CORTEX [J].
AVISSAR, S ;
SCHREIBER, G ;
AULAKH, CS ;
WOZNIAK, KM ;
MURPHY, DL .
EUROPEAN JOURNAL OF PHARMACOLOGY-MOLECULAR PHARMACOLOGY SECTION, 1990, 189 (01) :99-103