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New targets and therapeutics for neuroprotection, remyelination and repair in multiple sclerosis.多发性硬化症神经保护、髓鞘再生和修复的新靶点和治疗方法。
Expert Opin Investig Drugs. 2020 May;29(5):443-459. doi: 10.1080/13543784.2020.1757647. Epub 2020 Apr 29.
2
Regulation of Oligodendrocyte Functions: Targeting Lipid Metabolism and Extracellular Matrix for Myelin Repair.少突胶质细胞功能的调控:针对脂质代谢和细胞外基质进行髓鞘修复
J Clin Med. 2020 Feb 8;9(2):470. doi: 10.3390/jcm9020470.
3
Nav1.6 promotes inflammation and neuronal degeneration in a mouse model of multiple sclerosis.Nav1.6 促进多发性硬化症小鼠模型中的炎症和神经元变性。
J Neuroinflammation. 2019 Nov 13;16(1):215. doi: 10.1186/s12974-019-1622-1.
4
Monitoring retinal changes with optical coherence tomography predicts neuronal loss in experimental autoimmune encephalomyelitis.光学相干断层扫描监测视网膜变化可预测实验性自身免疫性脑脊髓炎中的神经元丢失。
J Neuroinflammation. 2019 Nov 4;16(1):203. doi: 10.1186/s12974-019-1583-4.
5
Using Acute Optic Neuritis Trials to Assess Neuroprotective and Remyelinating Therapies in Multiple Sclerosis.利用急性视神经炎试验评估多发性硬化症的神经保护和髓鞘修复疗法。
JAMA Neurol. 2020 Feb 1;77(2):234-244. doi: 10.1001/jamaneurol.2019.3283.
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The astrocyte transcriptome in EAE optic neuritis shows complement activation and reveals a sex difference in astrocytic C3 expression.实验性自身免疫性脑脊髓炎视神经炎中天麻细胞转录组显示补体激活,并揭示了星形胶质细胞 C3 表达的性别差异。
Sci Rep. 2019 Jul 10;9(1):10010. doi: 10.1038/s41598-019-46232-6.
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Oral lipoic acid as a treatment for acute optic neuritis: a blinded, placebo controlled randomized trial.口服硫辛酸治疗急性视神经炎:一项双盲、安慰剂对照的随机试验。
Mult Scler J Exp Transl Clin. 2019 May 13;5(2):2055217319850193. doi: 10.1177/2055217319850193. eCollection 2019 Apr-Jun.
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Gene expression in oligodendrocytes during remyelination reveals cholesterol homeostasis as a therapeutic target in multiple sclerosis.少突胶质细胞在髓鞘修复过程中的基因表达揭示胆固醇稳态是多发性硬化症的治疗靶点。
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9
Optical coherence tomography is highly sensitive in detecting prior optic neuritis.光学相干断层扫描在检测先前的视神经炎方面非常敏感。
Neurology. 2019 Feb 5;92(6):e527-e535. doi: 10.1212/WNL.0000000000006873. Epub 2019 Jan 23.
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Preclinical stress originates in the rat optic nerve head during development of autoimmune optic neuritis.临床前应激源于自身免疫性视神经炎发生过程中大鼠视神经头部。
Glia. 2019 Mar;67(3):512-524. doi: 10.1002/glia.23560. Epub 2018 Dec 21.

视神经炎的啮齿动物模型

Rodent Models of Optic Neuritis.

作者信息

Redler Yael, Levy Michael

机构信息

Department of Neuro-Ophthalmology, Massachusetts Eye & Ear Infirmary/Harvard Medical School, Boston, MA, United States.

Department of Neurology, Massachusetts General Hospital/Harvard Medical School, Boston, MA, United States.

出版信息

Front Neurol. 2020 Nov 3;11:580951. doi: 10.3389/fneur.2020.580951. eCollection 2020.

DOI:10.3389/fneur.2020.580951
PMID:33224094
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7669908/
Abstract

Optic neuritis (ON) is an inflammatory attack of the optic nerve that leads to visual disability. It is the most common optic neuropathy affecting healthy young adults, most commonly women aged 20-45 years. It can be idiopathic and monophasic or as part of a neurologic disease such as multiple sclerosis with recurrence and cumulative damage. Currently, there is no therapy to repair the damage from optic neuritis. Animal models are an essential tool for the understanding of the pathogenesis of optic neuritis and for the development of potential treatment strategies. Experimental autoimmune encephalomyelitis (EAE) is the most commonly used experimental rodent model for human autoimmune inflammatory demyelinating diseases of the central nervous system (CNS). In this review, we discuss the latest rodent models regarding optic neuritis, focusing on EAE model, and on its recent achievements and developments.

摘要

视神经炎(ON)是一种对视神经的炎性攻击,可导致视力残疾。它是影响健康年轻成年人的最常见的视神经病变,最常见于20至45岁的女性。它可以是特发性单相的,也可以是诸如多发性硬化症等神经系统疾病的一部分,具有复发和累积损伤。目前,尚无修复视神经炎损伤的疗法。动物模型是理解视神经炎发病机制和开发潜在治疗策略的重要工具。实验性自身免疫性脑脊髓炎(EAE)是用于人类中枢神经系统(CNS)自身免疫性炎性脱髓鞘疾病的最常用实验啮齿动物模型。在本综述中,我们讨论了有关视神经炎的最新啮齿动物模型,重点是EAE模型及其最近的成果和进展。