Behavioural and neurochemical effects of post-weaning social isolation in rodents - Relevance to developmental neuropsychiatric disorders

被引:686
作者
Fone, Kevin C. F. [1 ]
Porkess, M. Veronica [1 ]
机构
[1] Univ Nottingham, Sch Med, Queens Med Ctr, Sch Biomed Sci,Inst Neurosci, Nottingham NG7 2UH, England
关键词
social isolation; isolation rearing; schizophrenia; serotonin; dopamine; cognition; aggression; prepulse inhibition; neophobia; nucleus accumbens; hippocampus; frontal cortex;
D O I
10.1016/j.neubiorev.2008.03.003
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Exposing mammals to early-life adverse events, including maternal separation or social isolation, profoundly affects brain development and adult behaviour and may contribute to the occurrence of psychiatric disorders, such as depression and schizophrenia in genetically predisposed humans. The molecular mechanisms underlying these environmentally induced developmental adaptations are unclear and best evaluated in animal paradigms with translational salience. Rearing rat pups from to prevent social contact with conspecifics, produces reproducible, long-term weaning in isolation, changes including; neophobia, impaired sensorimotor gating, aggression, cognitive rigidity, reduced prefrontal cortical volume and decreased cortical and hippocampal synaptic plasticity. These alterations are associated with hyperfunction of mesolimbic dopaminergic systems, enhanced presynaptic dopamine (DA) and serotonergic (5-HT) function in the nucleus accumbens (NAcc), hypofunction of mesocortical DA and attenuated 5-HT function in the prefrontal cortex and hippocampus. These behavioural, morphological and neurochemical abnormalities, as reviewed herein, strongly resemble core features of schizophrenia. Therefore unravelling the mechanisms that trigger these sequelae will improve our knowledge of the aetiology of neurodevelopmental psychiatric disorders, enable identification of longitudinal biomarkers of dysfunction and permit predictive screening for novel compounds with potential antipsychotic efficacy. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1087 / 1102
页数:16
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