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目前模拟脑缺血再灌注和炎症的方法:从动物模型到血管化和神经免疫性脑类器官。

The current approaches to modeling the brain ischemia-reperfusion and inflammation: from animal models toward vascularized and neuroimmune cerebral organoids.

作者信息

Tregub Pavel P, Volegova Daria D, Berdnikov Arseniy K, Chekulaev Pavel A, Bystrov Daniil A, Komleva Yulia K, Kolotyeva Natalia A, Illarioshkin Sergey N, Salmina Alla B, Yurchenko Stanislav O

机构信息

Brain Science Institute, Research Center of Neurology, Volokolamskoye Highway, Moscow, 125367, Russia.

Department of Pathophysiology, I.M. Sechenov First Moscow State Medical University, Trubetskaya Street, Moscow, 119991, Russia.

出版信息

Rev Neurosci. 2025 May 28. doi: 10.1515/revneuro-2025-0015.

Abstract

For several decades, the modeling of brain diseases in experimental animals has remained one of the key components of studying the pathogenesis of central nervous system pathology and searching for new methods of prevention and therapy. In recent years, new approaches to modeling pathological conditions have been in active development; these approaches will not only reduce the number of animal studies but also allow us to take a step toward reproducing the human-specific mechanisms of brain pathology. In this review, we characterize the most common rodent models of cerebral ischemia and reperfusion, as well as neuroinflammation inherent to neurodegeneration (in particular, Parkinson's disease), which are reproduced . This review addresses engineering and technical challenges and the prospects for the development of brain pathology models , e.g., vascularized and microglia-containing/neuroimmune cerebral organoids, which may be useful in overcoming the shortcomings and limitations of the current models.

摘要

几十年来,实验动物脑疾病模型一直是研究中枢神经系统病理发病机制以及寻找预防和治疗新方法的关键组成部分之一。近年来,病理状况建模的新方法一直在积极发展;这些方法不仅将减少动物研究的数量,还将使我们朝着重现人类特有的脑病理机制迈进。在这篇综述中,我们描述了最常见的脑缺血再灌注啮齿动物模型,以及神经退行性变(特别是帕金森病)所固有的神经炎症,这些都是可以重现的。本综述探讨了工程和技术挑战以及脑病理模型的发展前景,例如血管化且含有小胶质细胞/神经免疫的脑类器官,它们可能有助于克服当前模型的缺点和局限性。

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