Ischemic stroke and diabetes: a TLR4-mediated neuroinflammatory perspective.

IF 4.8 3区 医学 Q1 GENETICS & HEREDITY
Journal of Molecular Medicine-Jmm Pub Date : 2024-06-01 Epub Date: 2024-03-28 DOI:10.1007/s00109-024-02441-9
Thura Tun Oo
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引用次数: 0

Abstract

Ischemic stroke is the major contributor to morbidity and mortality in people with diabetes mellitus. In ischemic stroke patients, neuroinflammation is now understood to be one of the main underlying mechanisms for cerebral damage and recovery delay. It has been well-established that toll-like receptor 4 (TLR4) signaling pathway plays a key role in neuroinflammation. Emerging research over the last decade has revealed that, compared to ischemic stroke without diabetes mellitus, ischemic stroke with diabetes mellitus significantly upregulates TLR4-mediated neuroinflammation, increasing the risk of cerebral and neuronal damage as well as neurofunctional recovery delay. This review aims to discuss how ischemic stroke with diabetes mellitus amplifies TLR4-mediated neuroinflammation and its consequences. Additionally covered in this review is the potential application of TLR4 antagonists in the management of diabetic ischemic stroke.

Abstract Image

缺血性中风与糖尿病:TLR4 介导的神经炎症视角。
缺血性中风是糖尿病患者发病和死亡的主要原因。在缺血性脑卒中患者中,神经炎症是导致脑损伤和恢复延迟的主要潜在机制之一。收费样受体 4(TLR4)信号通路在神经炎症中起着关键作用,这一点已得到证实。近十年来的新研究发现,与无糖尿病的缺血性卒中相比,糖尿病缺血性卒中会显著上调 TLR4 介导的神经炎症,增加脑和神经元损伤以及神经功能恢复延迟的风险。本综述旨在讨论缺血性中风合并糖尿病如何放大 TLR4 介导的神经炎症及其后果。此外,本综述还探讨了 TLR4 拮抗剂在糖尿病缺血性中风治疗中的潜在应用。
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来源期刊
Journal of Molecular Medicine-Jmm
Journal of Molecular Medicine-Jmm 医学-医学:研究与实验
CiteScore
9.30
自引率
0.00%
发文量
100
审稿时长
1.3 months
期刊介绍: The Journal of Molecular Medicine publishes original research articles and review articles that range from basic findings in mechanisms of disease pathogenesis to therapy. The focus includes all human diseases, including but not limited to: Aging, angiogenesis, autoimmune diseases as well as other inflammatory diseases, cancer, cardiovascular diseases, development and differentiation, endocrinology, gastrointestinal diseases and hepatology, genetics and epigenetics, hematology, hypoxia research, immunology, infectious diseases, metabolic disorders, neuroscience of diseases, -omics based disease research, regenerative medicine, and stem cell research. Studies solely based on cell lines will not be considered. Studies that are based on model organisms will be considered as long as they are directly relevant to human disease.
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