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血管生成与多发性硬化症发病机制:新型药物治疗方法一瞥

Angiogenesis and Multiple Sclerosis Pathogenesis: A Glance at New Pharmaceutical Approaches.

作者信息

Gentile Maria Teresa, Muto Gianluca, Lus Giacomo, Lövblad Karl-Olof, Svenningsen Åsa Fex, Colucci-D'Amato Luca

机构信息

Laboratory of Cellular and Molecular Neuropathology, Department of Environmental, Biological and Pharmaceutical Science and Technology, University of Campania "L. Vanvitelli", 81100 Caserta, Italy.

Division of Diagnostic and Interventional Neuroradiology, Geneva University Hospitals, 1205 Geneva, Switzerland.

出版信息

J Clin Med. 2022 Aug 9;11(16):4643. doi: 10.3390/jcm11164643.

DOI:10.3390/jcm11164643
PMID:36012883
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9410525/
Abstract

Multiple sclerosis is a chronic disease of the central nervous system characterized by demyelination and destruction of axons. The most common form of the disease is the relapsing-remitting multiple sclerosis in which episodic attacks with typical neurological symptoms are followed by episodes of partial or complete recovery. One of the underestimated factors that contribute to the pathogenesis of multiple sclerosis is excessive angiogenesis. Here, we review the role of angiogenesis in the onset and in the development of the disease, the molecular mechanisms underlying angiogenesis, the current therapeutic approaches, and the potential therapeutic strategies with a look at natural compounds as multi-target drugs with both neuroprotective and anti-angiogenic properties.

摘要

多发性硬化症是一种中枢神经系统的慢性疾病,其特征为脱髓鞘和轴突破坏。该疾病最常见的形式是复发缓解型多发性硬化症,其中典型神经症状的发作性发作之后是部分或完全恢复的阶段。促成多发性硬化症发病机制的一个被低估的因素是过度血管生成。在此,我们综述血管生成在该疾病的发病和发展中的作用、血管生成的分子机制、当前的治疗方法以及潜在的治疗策略,并着眼于天然化合物作为具有神经保护和抗血管生成特性的多靶点药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7bc/9410525/0f7a8247deba/jcm-11-04643-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7bc/9410525/0f7a8247deba/jcm-11-04643-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7bc/9410525/0f7a8247deba/jcm-11-04643-g001.jpg

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本文引用的文献

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Association of Brain Atrophy With Disease Progression Independent of Relapse Activity in Patients With Relapsing Multiple Sclerosis.脑萎缩与复发缓解型多发性硬化患者疾病进展的相关性,与复发活动无关。
JAMA Neurol. 2022 Jul 1;79(7):682-692. doi: 10.1001/jamaneurol.2022.1025.
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Astrocytes and Inflammatory T Helper Cells: A Dangerous Liaison in Multiple Sclerosis.星形胶质细胞和炎症辅助性 T 细胞:多发性硬化症中的危险联姻。
Front Immunol. 2022 Feb 8;13:824411. doi: 10.3389/fimmu.2022.824411. eCollection 2022.
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Pathophysiology of blood brain barrier dysfunction during chronic cerebral hypoperfusion in vascular cognitive impairment.
狨猴大脑中多发性硬化样病变演变的4D转录组图谱。
bioRxiv. 2023 Sep 27:2023.09.25.559371. doi: 10.1101/2023.09.25.559371.
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Oral Health Status and Multiple Sclerosis: Classic and Non-Classic Manifestations-Case Report.口腔健康状况与多发性硬化症:经典与非经典表现——病例报告
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血管性认知障碍慢性脑低灌注时血脑屏障功能障碍的病理生理学。
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Upregulation of miR-345-5p suppresses cell growth of lung adenocarcinoma by regulating ras homolog family member A (RhoA) and Rho/Rho associated protein kinase (Rho/ROCK) pathway.miR-345-5p 的上调通过调节 ras 同源家族成员 A(RhoA)和 Rho/Rho 相关蛋白激酶(Rho/ROCK)通路抑制肺腺癌细胞的生长。
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Growth Factors and Their Roles in Multiple Sclerosis Risk.生长因子及其在多发性硬化症风险中的作用。
Front Immunol. 2021 Oct 21;12:768682. doi: 10.3389/fimmu.2021.768682. eCollection 2021.
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Inflammation-Mediated Angiogenesis in Ischemic Stroke.缺血性卒中中炎症介导的血管生成
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J Mol Med (Berl). 2021 Aug;99(8):1033-1042. doi: 10.1007/s00109-021-02080-4. Epub 2021 May 5.
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