Histone deacetylase inhibitors: A novel strategy for neuroprotection and cardioprotection following ischemia/ reperfusion injury

27Citations
Citations of this article
25Readers
Mendeley users who have this article in their library.

Abstract

Ischemia/reperfusion injury is a complex molecular cascade that causes deleterious cellular damage and organ dysfunction. Stroke, sudden cardiac arrest, and acute myocardial infarction are the most common causes of ischemia/rep-erfusion injury without effective pharmacologic therapies. Existing preclinical evidence suggests that histone deacetylase inhibitors may be an efficacious, affordable, and clinically feasible therapy that can improve neurologic and cardiac outcomes following ischemia/reperfusion injury. In this review, we discuss the pathophysiology and epigenetic modulations of ischemia/ reperfusion injury and focus on the neuroprotective and cardioprotective effects of histone deacetylase inhibitors. We also summarize the protective effects of histone deacetylase inhibitors for other vital organs and highlight the key research priorities for their successful translation to the bedside.

Cite

CITATION STYLE

APA

Pickell, Z., Williams, A. M., Alam, H. B., & Hsu, C. H. (2020). Histone deacetylase inhibitors: A novel strategy for neuroprotection and cardioprotection following ischemia/ reperfusion injury. Journal of the American Heart Association, 9(11). https://doi.org/10.1161/JAHA.120.016349

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free