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非灵长类动物模型在理解精神分裂症病因学中的贡献。

Contribution of nonprimate animal models in understanding the etiology of schizophrenia.

机构信息

Department of Psychology, University of Western Ontario, London, Ont.

出版信息

J Psychiatry Neurosci. 2011 Jul;36(4):E5-29. doi: 10.1503/jpn.100054.

DOI:10.1503/jpn.100054
PMID:21247514
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3120891/
Abstract

Schizophrenia is a severe psychiatric disorder that is characterized by positive and negative symptoms and cognitive impairments. The etiology of the disorder is complex, and it is thought to follow a multifactorial threshold model of inheritance with genetic and neurodevelop mental contributions to risk. Human studies are particularly useful in capturing the richness of the phenotype, but they are often limited to the use of correlational approaches. By assessing behavioural abnormalities in both humans and rodents, nonprimate animal models of schizophrenia provide unique insight into the etiology and mechanisms of the disorder. This review discusses the phenomenology and etiology of schizophrenia and the contribution of current nonprimate animal models with an emphasis on how research with models of neuro transmitter dysregulation, environmental risk factors, neurodevelopmental disruption and genetic risk factors can complement the literature on schizophrenia in humans.

摘要

精神分裂症是一种严重的精神疾病,其特征是阳性和阴性症状以及认知障碍。该疾病的病因复杂,被认为遵循多因素阈模型遗传,遗传和神经发育对风险有贡献。人类研究在捕捉表型的丰富性方面特别有用,但它们通常仅限于使用相关方法。通过评估人类和啮齿动物的行为异常,精神分裂症的非灵长类动物模型提供了对该疾病病因和机制的独特见解。本文讨论了精神分裂症的发病机制和发病机制,以及当前非灵长类动物模型的贡献,重点介绍了神经递质失调模型、环境风险因素、神经发育中断和遗传风险因素的研究如何补充人类精神分裂症文献。

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本文引用的文献

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The Role of Biomarkers and Endophenotypes in Prevention and Treatment of Psychopathological Disorders.生物标志物和内表型在精神病理障碍预防与治疗中的作用
Biomark Med. 2009 Feb 1;3(1):1-3. doi: 10.2217/17520363.3.1.1.
2
Assessment of NMDA receptor NR1 subunit hypofunction in mice as a model for schizophrenia.评估 NMDA 受体 NR1 亚基功能低下在精神分裂症小鼠模型中的作用。
Genes Brain Behav. 2009 Oct;8(7):661-75. doi: 10.1111/j.1601-183X.2009.00504.x. Epub 2009 May 8.
3
Early postnatal depletion of NMDA receptor development affects behaviour and NMDA receptor expression until later adulthood in rats--a possible model for schizophrenia.早期 postnatal NMDA 受体发育耗竭影响大鼠成年后的行为和 NMDA 受体表达——一种可能的精神分裂症模型。
Behav Brain Res. 2009 Dec 14;205(1):96-101. doi: 10.1016/j.bbr.2009.06.018. Epub 2009 Jun 17.
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Presynaptic regulation of dopamine transmission in schizophrenia.精神分裂症中多巴胺传递的突触前调节。
Schizophr Bull. 2011 Jan;37(1):108-17. doi: 10.1093/schbul/sbp010. Epub 2009 Jun 12.
5
Analysis of prepulse inhibition in mouse lines overexpressing 22q11.2 orthologues.分析过表达 22q11.2 同源物的小鼠系的前脉冲抑制。
Int J Neuropsychopharmacol. 2009 Aug;12(7):983-9. doi: 10.1017/S1461145709000492. Epub 2009 Jun 11.
6
Working memory span and motor and cognitive speed in schizophrenia.精神分裂症中的工作记忆广度以及运动和认知速度
Cogn Behav Neurol. 2009 Jun;22(2):101-8. doi: 10.1097/WNN.0b013e3181a722a0.
7
Disc1 regulates granule cell migration in the developing hippocampus.Disc1在发育中的海马体中调节颗粒细胞迁移。
Hum Mol Genet. 2009 Sep 1;18(17):3286-97. doi: 10.1093/hmg/ddp266. Epub 2009 Jun 5.
8
How do psychiatric drugs work?精神科药物是如何起作用的?
BMJ. 2009 May 29;338:b1963. doi: 10.1136/bmj.b1963.
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Toward a model of impaired reality testing in rats.迈向大鼠现实检验受损模型
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DTNBP1, NRG1, DAOA, DAO and GRM3 polymorphisms and schizophrenia: an association study.DTNBP1、NRG1、DAOA、DAO和GRM3基因多态性与精神分裂症:一项关联研究。
Neuropsychobiology. 2009;59(3):142-50. doi: 10.1159/000218076. Epub 2009 May 12.