Perspectives for the development of animal models of bipolar disorder

被引:112
作者
Machado-Vieira, R
Kapczinski, F
Soares, JC
机构
[1] Univ Fed Rio Grande do Sul, Hosp Clin Porto Alegre, Lab Psiquiatria Expt, Ctr Pesquisas, BR-90035003 Porto Alegre, RS, Brazil
[2] Fdn Fac Fed Ciencias Med Porto Alegre, HMIPV, Mood Disorders Program, Porto Alegre, RS, Brazil
[3] Univ Sao Paulo, Sch Med, Doctoral Grad Program Psychiat, Sao Paulo, Brazil
[4] Univ Texas, Hlth Sci Ctr, Dept Psychiat, Div Mood & Anxiety Disorders, San Antonio, TX USA
[5] S Texas VA Hlth Care Syst, Audie L Murphy Div, San Antonio, TX USA
关键词
animal models; bipolar disorder; depression; etiology; mania; neurobiology; mood disorders;
D O I
10.1016/j.pnpbp.2003.10.015
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Bipolar disorder (BD) has been a particularly challenging illness for the development of adequate animal models for neurobiological studies. These difficulties are largely related to the peculiar clinical characteristics of this illness, with an intriguing alternation of mania, depression, euthymia, and mixed states. The etiology and brain mechanisms involved in this several mental illness remain unknown. Preclinical studies with animal models of mania or depression have been developed to evaluate the potential efficacy of new psychotropic drugs and generate information concerning the biochemical effects of these drugs on specific targets. These models try to mimic the behavioral components of mania and depression in human subjects and examine the pharmacological responses and mechanisms of action of potentially new therapeutic agents. The main limitation is that there is currently no model that would mimic mood cyclicity, which is a hallmark feature of BD. Thus, these models do not represent valid paradigms for the study of this illness, because they do not address key questions regarding cyclicity. In this review, we propose that new genetics approaches involving potential animal models of BD are a promising new area for further development. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:209 / 224
页数:16
相关论文
共 169 条
[11]   The time course of the hyperactivity that follows lesions or temporary inactivation of the fimbria-fornix [J].
Bannerman, DM ;
Gilmour, G ;
Norman, G ;
Lemaire, M ;
Iversen, SD ;
Rawlins, JNP .
BEHAVIOURAL BRAIN RESEARCH, 2001, 120 (01) :1-11
[12]   Sleep loss, a possible factor in augmenting manic episode [J].
Barbini, B ;
Bertelli, S ;
Colombo, C ;
Smeraldi, E .
PSYCHIATRY RESEARCH, 1996, 65 (02) :121-125
[13]  
BEAUREGARD M, 1996, CAN J BRAIN RES, V608, P216
[14]   Dopamine agonist amineptine prevents the antidepressant effect of sleep deprivation [J].
Benedetti, F ;
Barbini, B ;
Campori, E ;
Colombo, C ;
Smeraldi, E .
PSYCHIATRY RESEARCH, 1996, 65 (03) :179-184
[15]   Susceptibility loci for bipolar disorder: Overlap with inherited vulnerability to schizophrenia [J].
Berrettini, WH .
BIOLOGICAL PSYCHIATRY, 2000, 47 (03) :245-251
[16]   DOPAMINE FUNCTIONS IN APPETITIVE AND DEFENSIVE BEHAVIORS [J].
BLACKBURN, JR ;
PFAUS, JG ;
PHILLIPS, AG .
PROGRESS IN NEUROBIOLOGY, 1992, 39 (03) :247-279
[17]   Benzodiazepine and serotonergic modulation of antipredator and conspecific defense [J].
Blanchard, DC ;
Griebel, G ;
Rodgers, RJ ;
Blanchard, RJ .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 1998, 22 (05) :597-612
[18]  
BLAZER DG, 1994, AM J PSYCHIAT, V151, P979
[19]  
BLIER P, 1987, J CLIN PSYCHOPHARM, V7, pS24
[20]   CURRENT ADVANCES AND TRENDS IN THE TREATMENT OF DEPRESSION [J].
BLIER, P ;
DEMONTIGNY, C .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1994, 15 (07) :220-226