» Articles » PMID: 33144066

Emerging Neuroprotective Strategies for the Treatment of Ischemic Stroke: An Overview of Clinical and Preclinical Studies

Overview
Journal Exp Neurol
Specialty Neurology
Date 2020 Nov 4
PMID 33144066
Citations 235
Authors
Affiliations
Soon will be listed here.
Abstract

Stroke is the leading cause of disability and thesecond leading cause of death worldwide. With the global population aged 65 and over growing faster than all other age groups, the incidence of stroke is also increasing. In addition, there is a shift in the overall stroke burden towards younger age groups, particularly in low and middle-income countries. Stroke in most cases is caused due to an abrupt blockage of an artery (ischemic stroke), but in some instances stroke may be caused due to bleeding into brain tissue when a blood vessel ruptures (hemorrhagic stroke). Although treatment options for stroke are still limited, with the advancement in recanalization therapy using both pharmacological and mechanical thrombolysis some progress has been made in helping patients recover from ischemic stroke. However, there is still a substantial need for the development of therapeutic agents for neuroprotection in acute ischemic stroke to protect the brain from damage prior to and during recanalization, extend the therapeutic time window for intervention and further improve functional outcome. The current review has assessed the past challenges in developing neuroprotective strategies, evaluated the recent advances in clinical trials, discussed the recent initiative by the National Institute of Neurological Disorders and Stroke in USA for the search of novel neuroprotectants (Stroke Preclinical Assessment Network, SPAN) and identified emerging neuroprotectants being currently evaluated in preclinical studies. The underlying molecular mechanism of each of the neuroprotective strategies have also been summarized, which could assist in the development of future strategies for combinational therapy in stroke treatment.

Citing Articles

Combined transcriptomic and proteomic analyses reveal relevant myelin features in mice with ischemic stroke.

Qian Q, Lyu H, Wang W, Wang Q, Li D, Liu X Funct Integr Genomics. 2025; 25(1):64.

PMID: 40085348 DOI: 10.1007/s10142-025-01573-6.


Mechanism of KDM4A in Regulating Microglial Polarization in Ischemic Stroke.

Du J, Liang X, Wang D, Wang Z, Shen R Appl Biochem Biotechnol. 2025; .

PMID: 40080374 DOI: 10.1007/s12010-025-05207-2.


Pharmacological inhibition of carbonic anhydrases with a positively charged pyridinium sulfonamide phenocopies the neuroprotective effects of genetic ablation in a murine setting of oxygen/glucose deprivation followed by re-oxygenation and is....

Amiranda S, Succoio M, Anzilotti S, Cuomo O, Petrozziello T, Tedeschi V Heliyon. 2025; 11(4):e42457.

PMID: 40028587 PMC: 11868941. DOI: 10.1016/j.heliyon.2025.e42457.


Cerebrolysin as an adjuvant therapy after mechanical thrombectomy in large vessel occlusion cardioembolic stroke: a propensity score matching analysis.

ElBassiouny A, Shehata M, Zaki A, Bedros R, El-Sudany A, Nasser A Front Neurol. 2025; 16:1510284.

PMID: 40027163 PMC: 11868704. DOI: 10.3389/fneur.2025.1510284.


Impact of fracture fixation surgery on cognitive function and the gut microbiota in mice with a history of stroke.

Lu Y, Li Z, Xu R, Xu Y, Zhang W, Zhang Y Open Life Sci. 2025; 20(1):20221061.

PMID: 40026365 PMC: 11868713. DOI: 10.1515/biol-2022-1061.


References
1.
Ren C, Yan Z, Wei D, Gao X, Chen X, Zhao H . Limb remote ischemic postconditioning protects against focal ischemia in rats. Brain Res. 2009; 1288:88-94. PMC: 2744502. DOI: 10.1016/j.brainres.2009.07.029. View

2.
Lyden P, Levy H, Weymer S, Pryor K, Kramer W, Griffin J . Phase 1 safety, tolerability and pharmacokinetics of 3K3A-APC in healthy adult volunteers. Curr Pharm Des. 2013; 19(42):7479-85. PMC: 4040367. DOI: 10.2174/1381612819666131230131454. View

3.
Astrup J, Siesjo B, Symon L . Thresholds in cerebral ischemia - the ischemic penumbra. Stroke. 1981; 12(6):723-5. DOI: 10.1161/01.str.12.6.723. View

4.
Yagi K, Kitazato K, Uno M, Tada Y, Kinouchi T, Shimada K . Edaravone, a free radical scavenger, inhibits MMP-9-related brain hemorrhage in rats treated with tissue plasminogen activator. Stroke. 2008; 40(2):626-31. DOI: 10.1161/STROKEAHA.108.520262. View

5.
Berger J, Busto R, Ginsberg M . Verapamil: failure of metabolic amelioration following global forebrain ischemia in the rat. Stroke. 1984; 15(6):1029-32. DOI: 10.1161/01.str.15.6.1029. View