Challenges in understanding psychiatric disorders and developing therapeutics: a role for zebrafish

被引:30
作者
McCammon, Jasmine M. [1 ]
Sive, Hazel [1 ,2 ]
机构
[1] Whitehead Inst Biomed Res, Cambridge Ctr 9, 9 Cambridge Ctr, Cambridge, MA 02142 USA
[2] MIT, Dept Biol, Cambridge, MA 02139 USA
关键词
Zebrafish; Psychiatric disorders; Animal models; Co-morbidities; Chemical screens; Autism; Schizophrenia; FRAGILE-X-SYNDROME; COMORBIDITY SURVEY REPLICATION; PLURIPOTENT STEM-CELLS; DSM-IV DISORDERS; HUMAN-DISEASE; RETT-SYNDROME; NEUROPSYCHIATRIC DISORDERS; BRAIN-DEVELOPMENT; ANIMAL-MODELS; SYNAPTIC PLASTICITY;
D O I
10.1242/dmm.019620
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The treatment of psychiatric disorders presents three major challenges to the research and clinical community: defining a genotype associated with a disorder, characterizing the molecular pathology of each disorder and developing new therapies. This Review addresses how cellular and animal systems can help to meet these challenges, with an emphasis on the role of the zebrafish. Genetic changes account for a large proportion of psychiatric disorders and, as gene variants that predispose to psychiatric disease are beginning to be identified in patients, these are tractable for study in cellular and animal systems. Defining cellular and molecular criteria associated with each disorder will help to uncover causal physiological changes in patients and will lead to more objective diagnostic criteria. These criteria should also define co-morbid pathologies within the nervous system or in other organ systems. The definition of genotypes and of any associated pathophysiology is integral to the development of new therapies. Cell culture-based approaches can address these challenges by identifying cellular pathology and by high-throughput screening of gene variants and potential therapeutics. Whole-animal systems can define the broadest function of disorder-associated gene variants and the organismal impact of candidate medications. Given its evolutionary conservation with humans and its experimental tractability, the zebrafish offers several advantages to psychiatric disorder research. These include assays ranging from molecular to behavioural, and capability for chemical screening. There is optimism that the multiple approaches discussed here will link together effectively to provide new diagnostics and treatments for psychiatric patients.
引用
收藏
页码:647 / 656
页数:10
相关论文
共 128 条
[71]   Automated Large-Scale Culture and Medium-Throughput Chemical Screen for Modulators of Proliferation and Viability of Human Induced Pluripotent Stem Cell-Derived Neuroepithelial-like Stem Cells [J].
McLaren, Donna ;
Gorba, Thorsten ;
de Rotrou, Anita Marguerie ;
Pillai, Gopalan ;
Chappell, Clare ;
Stacey, Alison ;
Lingard, Sarah ;
Falk, Anna ;
Smith, Austin ;
Koch, Philipp ;
Bruestle, Oliver ;
Vickers, Richard ;
Tinsley, Jon ;
Flanders, David ;
Bello, Paul ;
Craig, Stewart .
JOURNAL OF BIOMOLECULAR SCREENING, 2013, 18 (03) :258-268
[72]   Evidence from in vivo imaging that synaptogenesis guides the growth and branching of axonal arbors by two distinct mechanisms [J].
Meyer, MP ;
Smith, SJ .
JOURNAL OF NEUROSCIENCE, 2006, 26 (13) :3604-3614
[73]   Repetitive behavior profile and supersensitivity to amphetamine in the C58/J mouse model of autism [J].
Moy, Sheryl S. ;
Riddick, Natallia V. ;
Nikolova, Viktoriya D. ;
Teng, Brian L. ;
Agster, Kara L. ;
Nonneman, Randal J. ;
Young, Nancy B. ;
Baker, Lorinda K. ;
Nadler, Jessica J. ;
Bodfish, James W. .
BEHAVIOURAL BRAIN RESEARCH, 2014, 259 :200-214
[74]   Medical co-morbidity risk factors and barriers to care for people with schizophrenia [J].
Muir-Cochrane, E. .
JOURNAL OF PSYCHIATRIC AND MENTAL HEALTH NURSING, 2006, 13 (04) :447-452
[75]   Effective targeted gene 'knockdown' in zebrafish [J].
Nasevicius, A ;
Ekker, SC .
NATURE GENETICS, 2000, 26 (02) :216-220
[76]   Animal models of cognitive dysfunction and negative symptoms of schizophrenia: Focus on NMDA receptor antagonism [J].
Neill, Joanna C. ;
Barnes, Samuel ;
Cook, Samantha ;
Grayson, Ben ;
Idris, Nagi F. ;
McLean, Samantha L. ;
Snigdha, Shikha ;
Rajagopal, Lakshmi ;
Harte, Michael K. .
PHARMACOLOGY & THERAPEUTICS, 2010, 128 (03) :419-432
[77]   Animal models of neuropsychiatric disorders [J].
Nestler, Eric J. ;
Hyman, Steven E. .
NATURE NEUROSCIENCE, 2010, 13 (10) :1161-1169
[78]   Behavioral and Synaptic Circuit Features in a Zebrafish Model of Fragile X Syndrome [J].
Ng, Ming-Chong ;
Yang, Yi-Ling ;
Lu, Kwok-Tung .
PLOS ONE, 2013, 8 (03)
[79]   Toward developmental models of psychiatric disorders in zebrafish [J].
Norton, William H. J. .
FRONTIERS IN NEURAL CIRCUITS, 2013, 7
[80]   Towards translational rodent models of depression [J].
O'Leary, Olivia F. ;
Cryan, John F. .
CELL AND TISSUE RESEARCH, 2013, 354 (01) :141-153