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本文引用的文献

1
Potential application as screening and drug designing tools of cytoarchitectural deficiencies present in three animal models of schizophrenia.潜在的应用作为筛选和药物设计工具的细胞构筑缺陷存在于三种精神分裂症动物模型。
Expert Opin Drug Discov. 2009 Mar;4(3):257-78. doi: 10.1517/17460440902762794.
2
Influence of social isolation in the rat on serotonergic function and memory--relevance to models of schizophrenia and the role of 5-HT₆ receptors.社交隔离对大鼠 5-羟色胺能功能和记忆的影响——与精神分裂症模型的相关性及 5-HT₆受体的作用。
Neuropharmacology. 2011 Sep;61(3):400-7. doi: 10.1016/j.neuropharm.2011.03.003. Epub 2011 Mar 15.
3
Blockade of dopamine D₃ but not D₂ receptors reverses the novel object discrimination impairment produced by post-weaning social isolation: implications for schizophrenia and its treatment.阻断多巴胺 D₃ 受体而非 D₂ 受体可逆转幼年期社交隔离导致的新物体辨别障碍:对精神分裂症及其治疗的启示。
Int J Neuropsychopharmacol. 2012 May;15(4):471-84. doi: 10.1017/S1461145711000435. Epub 2011 Mar 18.
4
Pharmacological characterization of social isolation-induced hyperactivity.社交隔离诱导多动性的药理学特征。
Psychopharmacology (Berl). 2011 May;215(2):257-66. doi: 10.1007/s00213-010-2128-9. Epub 2010 Dec 31.
5
Phenotypic characterization of transgenic mice overexpressing neuregulin-1.过表达神经调节蛋白-1 的转基因小鼠的表型特征。
PLoS One. 2010 Dec 9;5(12):e14185. doi: 10.1371/journal.pone.0014185.
6
Prenatal interaction of mutant DISC1 and immune activation produces adult psychopathology.突变 DISC1 与免疫激活的产前相互作用可产生成年精神病理学。
Biol Psychiatry. 2010 Dec 15;68(12):1172-81. doi: 10.1016/j.biopsych.2010.09.022.
7
The environment and schizophrenia.环境与精神分裂症。
Nature. 2010 Nov 11;468(7321):203-12. doi: 10.1038/nature09563.
8
Reduced dysbindin expression mediates N-methyl-D-aspartate receptor hypofunction and impaired working memory performance.减少双调蛋白表达介导 N-甲基-D-天冬氨酸受体功能低下和工作记忆表现受损。
Biol Psychiatry. 2011 Jan 1;69(1):28-34. doi: 10.1016/j.biopsych.2010.09.012. Epub 2010 Oct 30.
9
Dysbindin-1 modulates prefrontal cortical activity and schizophrenia-like behaviors via dopamine/D2 pathways.Dysbindin-1 通过多巴胺/D2 途径调节前额叶皮层活动和类似精神分裂症的行为。
Mol Psychiatry. 2012 Jan;17(1):85-98. doi: 10.1038/mp.2010.106. Epub 2010 Oct 19.
10
The environment and susceptibility to schizophrenia.环境与精神分裂症易感性。
Prog Neurobiol. 2011 Jan;93(1):23-58. doi: 10.1016/j.pneurobio.2010.09.003. Epub 2010 Oct 16.

精神分裂症的动物模型。

Animal models of schizophrenia.

机构信息

School of Biomedical Sciences, Medical School, Queen's Medical Centre, The University of Nottingham, Nottingham, UK.

出版信息

Br J Pharmacol. 2011 Oct;164(4):1162-94. doi: 10.1111/j.1476-5381.2011.01386.x.

DOI:10.1111/j.1476-5381.2011.01386.x
PMID:21449915
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3229756/
Abstract

Developing reliable, predictive animal models for complex psychiatric disorders, such as schizophrenia, is essential to increase our understanding of the neurobiological basis of the disorder and for the development of novel drugs with improved therapeutic efficacy. All available animal models of schizophrenia fit into four different induction categories: developmental, drug-induced, lesion or genetic manipulation, and the best characterized examples of each type are reviewed herein. Most rodent models have behavioural phenotype changes that resemble 'positive-like' symptoms of schizophrenia, probably reflecting altered mesolimbic dopamine function, but fewer models also show altered social interaction, and learning and memory impairment, analogous to negative and cognitive symptoms of schizophrenia respectively. The negative and cognitive impairments in schizophrenia are resistant to treatment with current antipsychotics, even after remission of the psychosis, which limits their therapeutic efficacy. The MATRICS initiative developed a consensus on the core cognitive deficits of schizophrenic patients, and recommended a standardized test battery to evaluate them. More recently, work has begun to identify specific rodent behavioural tasks with translational relevance to specific cognitive domains affected in schizophrenia, and where available this review focuses on reporting the effect of current and potential antipsychotics on these tasks. The review also highlights the need to develop more comprehensive animal models that more adequately replicate deficits in negative and cognitive symptoms. Increasing information on the neurochemical and structural CNS changes accompanying each model will also help assess treatments that prevent the development of schizophrenia rather than treating the symptoms, another pivotal change required to enable new more effective therapeutic strategies to be developed.

摘要

开发可靠的、可预测的复杂精神疾病(如精神分裂症)的动物模型对于增加我们对该疾病神经生物学基础的理解以及开发具有改善治疗效果的新型药物至关重要。所有现有的精神分裂症动物模型都可以归入四个不同的诱导类别:发育、药物诱导、损伤或遗传操作,本文回顾了每种类型的最佳特征示例。大多数啮齿动物模型都有类似于精神分裂症“阳性症状”的行为表型变化,可能反映了中脑边缘多巴胺功能的改变,但较少的模型也显示出社交互动和学习记忆障碍,分别类似于精神分裂症的阴性和认知症状。精神分裂症的阴性和认知障碍对当前抗精神病药物的治疗有抵抗力,即使在精神病缓解后也是如此,这限制了它们的治疗效果。MATRICS 倡议就精神分裂症患者的核心认知缺陷达成了共识,并建议使用标准化的测试组合来评估这些缺陷。最近,人们开始识别与精神分裂症中受影响的特定认知领域具有转化相关性的特定啮齿动物行为任务,在有可用信息的情况下,本综述侧重于报告当前和潜在的抗精神病药物对这些任务的影响。该综述还强调需要开发更全面的动物模型,以更充分地复制阴性和认知症状的缺陷。增加伴随每种模型的神经化学和结构中枢神经系统变化的信息也将有助于评估预防精神分裂症发展而不是治疗症状的治疗方法,这是开发新的、更有效的治疗策略所必需的另一个关键变化。