Key result
ALDH2 activators and ALDH bright cells show promise for reducing cardiac and cerebral ischemia-reperfusion injury.
Why the study?
Accumulation of toxic aldehydes is an important mechanism for myocardial and cerebral ischemia/reperfusion injury, and ALDH2 plays a major role in their clearance, suggesting it as a potential drug target for protection.
Do ALDH2 activators or ALDH(br) cells protect the heart and brain from ischemia/reperfusion injury?
Do ALDH2 activators or ALDH(br) cells protect the heart and brain from ischemia/reperfusion injury?
ALDH2 activators and ALDH(br) cells represent promising therapeutic targets for mitigating myocardial and cerebral ischemia/reperfusion injury.
ALDH2 activators should not yet alter ischemia/reperfusion management; leaves open their therapeutic translation pending clinical trials.
Mitochondrial aldehyde dehydrogenase (ALDH2) is an isoenzyme of aldehyde dehydrogenases (ALDH), a group of enzymes that are responsible for clearance of aldehydes in the body. In animal myocardial or cerebral ischemia/ reperfusion (I/R) models, accumulation of toxic aldehydes, such as 4-hydroxy-2-nonenal and malondialdehyde, is thought to be an important mechanism for myocardial and cerebral I/R injury. Among the isoenzymes of ALDH, ALDH2 is believed to play a major role in clearance of toxic aldehydes. Thus, ALDH2 might be a potential drug target for protection of the heart or brain from I/R injury. Indeed, some of the newly identified ALDH2 activators (such as Alda-1) have demonstrated beneficial effects on heart and brain I/R injury. In addition, ALDH activity is present at high levels in some stem or progenitor cells, known as ALDH bright (ALDH(br)) cells, which possess potential value in treating patients with myocardial ischemia. The main purpose of this review is 1) to summarize recent findings regarding the role of ALDH2 in protection of heart or brain from I/R injury, 2) to list the available ALDH2 activators with their potency, selectivity and clinical potentials, and 3) to provide a rationale for ALDH(br) cells in clinical therapeutic value.
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Luo et al. (2014) conducted a review in Ischemia/reperfusion injury. ALDH2 activators and ALDH bright cells was evaluated. ALDH2 activators and ALDH bright cells represent potential therapeutic targets for protecting the heart and brain from ischemia/reperfusion injury.
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