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中枢神经系统脱髓鞘模型中的行为表型。

Behavioural phenotypes in the cuprizone model of central nervous system demyelination.

机构信息

School of Medicine, Western Sydney University, New South Wales, Australia.

Departments of Health Sciences and Biological Sciences, Faculties of Applied Health Sciences and Mathematics & Science, Brock University, Ontario, Canada.

出版信息

Neurosci Biobehav Rev. 2019 Dec;107:23-46. doi: 10.1016/j.neubiorev.2019.08.008. Epub 2019 Aug 21.

Abstract

The feeding of cuprizone (CPZ) to animals has been extensively used to model the processes of demyelination and remyelination, with many papers adopting a narrative linked to demyelinating conditions like multiple sclerosis (MS), the aetiology of which is unknown. However, no current animal model faithfully replicates the myriad of symptoms seen in the clinical condition of MS. CPZ ingestion causes mitochondrial and endoplasmic reticulum stress and subsequent apoptosis of oligodendrocytes leads to central nervous system demyelination and glial cell activation. Although there are a wide variety of behavioural tests available for characterizing the functional deficits in animal models of disease, including that of CPZ-induced deficits, they have focused on a narrow subset of outcomes such as motor performance, cognition, and anxiety. The literature has not been systematically reviewed in relation to these or other symptoms associated with clinical MS. This paper reviews these tests and makes recommendations as to which are the most important in order to better understand the role of this model in examining aspects of demyelinating diseases like MS.

摘要

给予动物服用铜蓝蛋白(CPZ)已被广泛用于模拟脱髓鞘和髓鞘再生过程,许多论文采用了一种叙述方式,将其与多发性硬化症(MS)等脱髓鞘疾病联系起来,而 MS 的病因尚不清楚。然而,目前没有任何动物模型能忠实地复制出 MS 临床症状的多样性。CPZ 摄入会导致线粒体和内质网应激,随后少突胶质细胞凋亡会导致中枢神经系统脱髓鞘和神经胶质细胞激活。尽管有各种各样的行为测试可用于描述疾病动物模型中的功能缺陷,包括 CPZ 诱导的缺陷,但它们主要集中在运动表现、认知和焦虑等狭窄的结果子集上。关于与临床 MS 相关的这些或其他症状,文献尚未对此进行系统综述。本文综述了这些测试,并就哪些测试最重要提出了建议,以便更好地理解该模型在检查多发性硬化症等脱髓鞘疾病方面的作用。

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