Update on current animal models for schizophrenia: are they still useful?

被引:6
作者
Uliana, Daniela L. [1 ,2 ,3 ]
Gomes, Felipe V. [4 ]
Grace, Anthony A. [1 ,2 ,3 ,5 ]
机构
[1] Univ Pittsburgh, Dept Neurosci, Pittsburgh, PA USA
[2] Univ Pittsburgh, Dept Psychiat, Pittsburgh, PA USA
[3] Univ Pittsburgh, Dept Psychol, Pittsburgh, PA USA
[4] Univ Sao Paulo, Ribeirao Preto Med Sch, Dept Pharmacol, Ribeirao Preto, SP, Brazil
[5] Univ Pittsburgh, Dept Neurosci, A210 Langley Hall, Pittsburgh, PA 15260 USA
基金
巴西圣保罗研究基金会; 美国国家卫生研究院;
关键词
animal models; antipsychotics; dopamine; schizophrenia; DEVELOPMENTAL DISRUPTION MODEL; MATERNAL IMMUNE ACTIVATION; METHYLAZOXYMETHANOL ACETATE; DOPAMINE SYSTEM; PHARMACOLOGICAL CHARACTERIZATION; RAT MODEL; STRESS; DYSREGULATION; PATHOPHYSIOLOGY; INTERNEURONS;
D O I
10.1097/YCO.0000000000000854
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Purpose of reviewSchizophrenia is a psychiatric disorder that has a significant socioeconomic impact worldwide. Antipsychotic drugs targeting dopamine transmission alleviate psychotic symptoms but with limited efficacy and tolerability. Animal models have long proven useful for drug discovery. The continued need for new treatment highlights the importance of animal models to study schizophrenia. The lack of new therapeutic compounds combined with the shortcomings of clinical design studies potentially decreased the enthusiasm for animal model use.Recent findingsIn the current review, we discuss the central role of animal models for schizophrenia in providing new insights into neurobiological features and therapeutic development. The US National Institute of Mental Health released the Research Domain Criteria to guide preclinical model studies. Here, we point out the advances of this approach and debate its potential limitations when using animal models to study schizophrenia from the drug discovery perspective.Cross-validated animal models for schizophrenia are crucial to comprehend the cause, pathophysiology, and behavioral and biological features of the disease, to advance prevention and treatment, and the need to carefully evaluate and select appropriate paradigms when investigating novel therapeutic targets.
引用
收藏
页码:172 / 178
页数:7
相关论文
共 69 条
[1]   Genetic risk for bipolar disorder and schizophrenia predicts structure and function of the ventromedial prefrontal cortex [J].
Abe, Christoph ;
Petrovic, Predrag ;
Ossler, William ;
Thompson, William H. ;
Liberg, Benny ;
Song, Jie ;
Bergen, Sarah E. ;
Sellgren, Carl M. ;
Fransson, Peter ;
Ingvar, Martin ;
Landen, Mikael .
JOURNAL OF PSYCHIATRY & NEUROSCIENCE, 2021, 46 (04) :E441-E450
[2]  
Agid O, 2006, J PSYCHIATR NEUROSCI, V31, P93
[3]   Glycine reuptake inhibitor RG1678: A pharmacologic characterization of an investigational agent for the treatment of schizophrenia [J].
Alberati, Daniela ;
Moreau, Jean-Luc ;
Lengyel, Judith ;
Hauser, Nicole ;
Mory, Roland ;
Borroni, Edilio ;
Pinard, Emmanuel ;
Knoflach, Frederic ;
Schlotterbeck, Goetz ;
Hainzl, Dominik ;
Wettstein, Joseph G. .
NEUROPHARMACOLOGY, 2012, 62 (02) :1152-1161
[4]  
BARR CE, 1990, ARCH GEN PSYCHIAT, V47, P869
[5]   Childhood Trauma May Increase Risk of Psychosis and Mood Disorder in Genetically High-risk Children and Adolescents by Enhancing the Accumulation of Risk Indicators [J].
Berthelot, Nicolas ;
Garon-Bissonnette, Julia ;
Jomphe, Valerie ;
Doucet-Beaupre, Helene ;
Bureau, Alexandre ;
Maziade, Michel .
SCHIZOPHRENIA BULLETIN OPEN, 2022, 3 (01)
[6]   USING HUMAN BRAIN IMAGING STUDIES AS A GUIDE TOWARD ANIMAL MODELS OF SCHIZOPHRENIA [J].
Bolkan, S. S. ;
Poyraz, F. Carvalho ;
Kellendonk, C. .
NEUROSCIENCE, 2016, 321 :77-98
[7]   ACUTE AND CHRONIC HALOPERIDOL TREATMENT - COMPARISON OF EFFECTS ON NIGRAL DOPAMINERGIC CELL ACTIVITY [J].
BUNNEY, BS ;
GRACE, AA .
LIFE SCIENCES, 1978, 23 (16) :1715-1727
[8]  
Cardno AG, 2000, AM J MED GENET, V97, P12, DOI 10.1002/(SICI)1096-8628(200021)97:1<12::AID-AJMG3>3.0.CO
[9]  
2-U
[10]  
CARLSSON A, 1963, ACTA PHARMACOL TOX, V20, P140