• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

斑马鱼作为多发性硬化症的模型

Zebrafish as a Model for Multiple Sclerosis.

作者信息

Maktabi Briana, Collins Abigail, Safee Raihaanah, Bouyer Jada, Wisner Alexander S, Williams Frederick E, Schiefer Isaac T

机构信息

Department of Pharmacology and Experimental Therapeutics, University of Toledo, Toledo, OH 43614, USA.

Center for Drug Design and Development 3, University of Toledo, Toledo, OH 43614, USA.

出版信息

Biomedicines. 2024 Oct 16;12(10):2354. doi: 10.3390/biomedicines12102354.

DOI:10.3390/biomedicines12102354
PMID:39457666
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11504653/
Abstract

Zebrafish have become a key model organism in neuroscience research because of their unique advantages. Their genetic, anatomical, and physiological similarities to humans, coupled with their rapid development and transparent embryos, make them an excellent tool for investigating various aspects of neurobiology. They have specifically emerged as a valuable and versatile model organism in biomedical research, including the study of neurological disorders such as multiple sclerosis. Multiple sclerosis is a chronic autoimmune disease known to cause damage to the myelin sheath that protects the nerves in the brain and spinal cord. This review emphasizes the importance of continued research in both in vitro and in vivo models to advance our understanding of MS and develop effective treatments, ultimately improving the quality of life for those affected by this debilitating disease. Recent studies show the significance of zebrafish as a model organism for investigating demyelination and remyelination processes, providing new insights into MS pathology and potential therapies.

摘要

由于其独特的优势,斑马鱼已成为神经科学研究中的关键模式生物。它们在基因、解剖学和生理学上与人类相似,再加上其发育迅速且胚胎透明,使其成为研究神经生物学各个方面的优秀工具。它们尤其已成为生物医学研究中有价值且通用的模式生物,包括对诸如多发性硬化症等神经系统疾病的研究。多发性硬化症是一种慢性自身免疫性疾病,已知会对保护大脑和脊髓神经的髓鞘造成损害。 本综述强调了在体外和体内模型中持续开展研究对于增进我们对多发性硬化症的理解并开发有效治疗方法的重要性,最终改善受这种使人衰弱疾病影响者的生活质量。 最近的研究表明斑马鱼作为研究脱髓鞘和髓鞘再生过程的模式生物的重要性,为多发性硬化症病理学和潜在疗法提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11d7/11504653/46917dde0f0d/biomedicines-12-02354-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11d7/11504653/46917dde0f0d/biomedicines-12-02354-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11d7/11504653/46917dde0f0d/biomedicines-12-02354-g001.jpg

相似文献

1
Zebrafish as a Model for Multiple Sclerosis.斑马鱼作为多发性硬化症的模型
Biomedicines. 2024 Oct 16;12(10):2354. doi: 10.3390/biomedicines12102354.
2
Cryogel scaffolds for regionally constrained delivery of lysophosphatidylcholine to central nervous system slice cultures: A model of focal demyelination for multiple sclerosis research.用于将溶血磷脂酰胆碱区域性限制递送至中枢神经系统切片培养物的水凝胶支架:多发性硬化症研究的局灶性脱髓鞘模型。
Acta Biomater. 2019 Oct 1;97:216-229. doi: 10.1016/j.actbio.2019.08.030. Epub 2019 Aug 16.
3
Recent Advances on Immunosuppressive Drugs and Remyelination Enhancers for the Treatment of Multiple Sclerosis.近年来用于多发性硬化症治疗的免疫抑制药物和髓鞘再生增强剂的研究进展。
Curr Pharm Des. 2021 Oct 5;27(30):3273-3280. doi: 10.2174/1381612827666210127121829.
4
Modeling demyelination and endogenous remyelination in spinal cord rat organotypic slice cultures.脊髓大鼠器官型切片培养中脱髓鞘和内源性髓鞘再生的建模
Front Cell Neurosci. 2024 Jun 26;18:1345042. doi: 10.3389/fncel.2024.1345042. eCollection 2024.
5
A Novel Lysolecithin Model for Visualizing Damage in the Larval Zebrafish Spinal Cord.一种用于可视化斑马鱼幼体脊髓损伤的新型溶血卵磷脂模型。
Front Cell Dev Biol. 2021 May 20;9:654583. doi: 10.3389/fcell.2021.654583. eCollection 2021.
6
Development of zebrafish demyelination model for evaluation of remyelination compounds and RORγt inhibitors.用于评估髓鞘再生化合物和RORγt抑制剂的斑马鱼脱髓鞘模型的开发。
J Pharmacol Toxicol Methods. 2019 Jul-Aug;98:106585. doi: 10.1016/j.vascn.2019.106585. Epub 2019 May 18.
7
Multiple Sclerosis: Basic and Clinical.多发性硬化症:基础与临床
Adv Neurobiol. 2017;15:211-252. doi: 10.1007/978-3-319-57193-5_8.
8
Cell reprogramming for oligodendrocytes: A review of protocols and their applications to disease modeling and cell-based remyelination therapies.细胞重编程为少突胶质细胞:方案综述及其在疾病建模和基于细胞的髓鞘修复治疗中的应用。
J Neurosci Res. 2023 Jun;101(6):1000-1028. doi: 10.1002/jnr.25173. Epub 2023 Feb 7.
9
Demyelination versus remyelination in progressive multiple sclerosis.进行性多发性硬化中的脱髓鞘与髓鞘再生。
Brain. 2010 Oct;133(10):2983-98. doi: 10.1093/brain/awq250. Epub 2010 Sep 20.
10
Targeting Oligodendrocyte Dynamics and Remyelination: Emerging Therapies and Personalized Approaches in Multiple Sclerosis Management.靶向少突胶质细胞动力学与髓鞘再生:多发性硬化症治疗中的新兴疗法与个性化方法
Curr Neurovasc Res. 2025;21(4):359-417. doi: 10.2174/0115672026336440240822063430.

本文引用的文献

1
Clinically isolated syndrome: Diagnosis and risk of developing clinically definite multiple sclerosis.临床孤立综合征:诊断和发展为临床确诊多发性硬化症的风险。
Neurologia (Engl Ed). 2023 Nov-Dec;38(9):663-670. doi: 10.1016/j.nrleng.2021.01.010. Epub 2023 Oct 17.
2
Smouldering Lesion in MS: Microglia, Lymphocytes and Pathobiochemical Mechanisms.多发性硬化症中的潜伏性病灶:小胶质细胞、淋巴细胞和病理生物化学机制。
Int J Mol Sci. 2023 Aug 10;24(16):12631. doi: 10.3390/ijms241612631.
3
Antibodies from serum and CSF of multiple sclerosis patients bind to oligodendroglial and neuronal cell-lines.
来自多发性硬化症患者血清和脑脊液的抗体与少突胶质细胞系和神经元细胞系结合。
Brain Commun. 2023 May 23;5(3):fcad164. doi: 10.1093/braincomms/fcad164. eCollection 2023.
4
Zebrafish as a model organism for neurodegenerative disease.斑马鱼作为神经退行性疾病的模式生物。
Front Mol Neurosci. 2022 Oct 13;15:940484. doi: 10.3389/fnmol.2022.940484. eCollection 2022.
5
Automated synapse-level reconstruction of neural circuits in the larval zebrafish brain.自动重建幼虫斑马鱼大脑中的神经回路突触水平。
Nat Methods. 2022 Nov;19(11):1357-1366. doi: 10.1038/s41592-022-01621-0. Epub 2022 Oct 24.
6
Ocrelizumab: A Review in Multiple Sclerosis.奥瑞珠单抗:多发性硬化症的治疗药物。
Drugs. 2022 Feb;82(3):323-334. doi: 10.1007/s40265-022-01672-9. Epub 2022 Feb 22.
7
How patients with multiple sclerosis acquire disability.多发性硬化症患者如何致残。
Brain. 2022 Sep 14;145(9):3147-3161. doi: 10.1093/brain/awac016.
8
Cuprizone-induced dopaminergic hyperactivity and locomotor deficit in zebrafish larvae.杯状病毒诱导的斑马鱼幼体多巴胺能活性亢进和运动缺陷。
Brain Res. 2022 Apr 1;1780:147802. doi: 10.1016/j.brainres.2022.147802. Epub 2022 Jan 24.
9
The semantics of microglia activation: neuroinflammation, homeostasis, and stress.小胶质细胞激活的语义:神经炎症、内稳态和应激。
J Neuroinflammation. 2021 Nov 6;18(1):258. doi: 10.1186/s12974-021-02309-6.
10
Secondary Progressive Multiple Sclerosis: New Insights.继发进展型多发性硬化症:新的认识。
Neurology. 2021 Aug 24;97(8):378-388. doi: 10.1212/WNL.0000000000012323. Epub 2021 Jun 4.