Schizophrenia an depression co-morbidity: what we have learned from animal models

被引:66
作者
Samsom, James N. [1 ,2 ]
Wong, Albert H. C. [1 ,2 ,3 ]
机构
[1] Ctr Addict & Mental Hlth, Campbell Family Mental Hlth Res Inst, Dept Mol Neurosci, Toronto, ON M5T 1R8, Canada
[2] Univ Toronto, Dept Pharmacol, Fac Med, Toronto, ON, Canada
[3] Univ Toronto, Fac Med, Dept Psychiat, Toronto, ON M5S 1A1, Canada
关键词
mouse; schizophrenia; depression; animal model; genetics; CATECHOL-O-METHYLTRANSFERASE; MATERNAL IMMUNE ACTIVATION; HETEROZYGOUS REELER MOUSE; MEDIAL PREFRONTAL CORTEX; GENOME-WIDE ASSOCIATION; NEUROTROPHIC FACTOR EXPRESSION; POSTWEANING SOCIAL-ISOLATION; LONG-TERM POTENTIATION; PREPULSE INHIBITION REGULATION; GENE-ENVIRONMENT INTERACTIONS;
D O I
10.3389/fpsyt.2015.00013
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Patients with schizophrenia are at an increased risk for the development of depression. Overlap in the symptoms and genetic risk factors between the two disorders suggests a common etiological mechanism may underlie the presentation of comorbid depression in schizophrenia. Understanding these shared mechanisms will be important in informing the development of new treatments. Rodent models are powerful tools for understanding gene function as it relates to behavior. Examining rodent models relevant to both schizophrenia and depression reveals a number of common mechanisms. Current models which demonstrate endophenotypes of both schizophrenia and depression are reviewed here, including models of CUB and SUSHI multiple domains 1, PDZ and LIM domain 5, glutamate Delta 1 receptor, diabetic db/db mice, neuropeptide Y, disrupted in schizophrenia 1, and its interacting partners, reelin, maternal immune activation, and social isolation. Neurotransmission, brain connectivity, the immune system, the environment, and metabolism emerge as potential common mechanisms linking these models and potentially explaining comorbid depression in schizophrenia.
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页数:24
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