Understanding the Pathophysiology of Ischemic Stroke: The Basis of Current Therapies and Opportunity for New Ones

被引:19
|
作者
Salaudeen, Maryam A. [1 ,2 ]
Bello, Nura [2 ,3 ]
Danraka, Rabiu N. [2 ,6 ]
Ammani, Maryam L. [4 ,5 ]
机构
[1] Univ Manchester, Fac Biol Med & Hlth, Sch Biol Sci, Div Neurosci, Manchester M13 9PL, England
[2] Ahmadu Bello Univ, Fac Pharmaceut Sci, Dept Pharmacol & Therapeut, Zaria 810107, Nigeria
[3] Usmanu Danfodiyo Univ, Coll Hlth Sci, Fac Clin Sci, Dept Pharmacol & Therapeut, Sokoto 840001, Nigeria
[4] Nottingham Trent Univ, Sch Sci & Technol, Dept Biosci, Nottingham NG11 8NS, England
[5] Kaduna State Univ, Fac Pharmaceut Sci, Dept Pharmacol & Toxicol, Kaduna 800283, Nigeria
[6] Jiangxi Univ Tradit Chinese Med, Dept Pharmacol & Toxicol, Nanchang 330004, Peoples R China
关键词
ischemic stroke; neuroinflammation; oxidative stress; neuroprotection; cellular therapy; drug repurposing; CEREBRAL-ARTERY OCCLUSION; ACUTE CORONARY SYNDROMES; INDIVIDUAL PATIENT DATA; MESENCHYMAL STEM-CELLS; CYCLOSPORINE-A; NEURONAL DEATH; DOUBLE-BLIND; INTRAVENOUS ANCROD; APOPTOTIC PATHWAY; EARLY MANAGEMENT;
D O I
10.3390/biom14030305
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The majority of approved therapies for many diseases are developed to target their underlying pathophysiology. Understanding disease pathophysiology has thus proven vital to the successful development of clinically useful medications. Stroke is generally accepted as the leading cause of adult disability globally and ischemic stroke accounts for the most common form of the two main stroke types. Despite its health and socioeconomic burden, there is still minimal availability of effective pharmacological therapies for its treatment. In this review, we take an in-depth look at the etiology and pathophysiology of ischemic stroke, including molecular and cellular changes. This is followed by a highlight of drugs, cellular therapies, and complementary medicines that are approved or undergoing clinical trials for the treatment and management of ischemic stroke. We also identify unexplored potential targets in stroke pathogenesis that can be exploited to increase the pool of effective anti-stroke and neuroprotective agents through de novo drug development and drug repurposing.
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收藏
页数:23
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