Key result
Central donepezil microinfusion improves 160-day survival by ~36 percentage points in heart failure rats.
Why the study?
The mechanisms underlying the cardioprotective effects of donepezil in chronic heart failure remain totally unknown.
Oral administration of donepezil, a centrally acting acetylcholinesterase inhibitor, improves the survival of rats with chronic heart failure (CHF). The mechanisms of cardioprotective effects of donepezil, however, remain totally unknown. To elucidate potential mechanisms, we examined whether central microinfusion of donepezil would exert cardioprotection. Intracerebroventricular microinfusion pumps with cerebroventricular cannula were implanted in rats with myocardial infarction. The rats were randomly divided into central saline treatment (CST) and central donepezil treatment (CDT) groups. We evaluated cardiac remodeling and function after a 6-week treatment and examined the 160-day survival rate. Compared to the CST, the CDT markedly improved the 160-day survival rate (68% vs. 32%, P = 0.002) through the prevention of cardiac remodeling and the lowering of plasma catecholamine, brain natriuretic peptide, and angiotensin II. These results suggest that the central mechanism plays an important role in the cardioprotective effects of donepezil.
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Li et al. (2020) studied Chronic heart failure (n=88). Donepezil intracerebroventricular microinfusion vs. Central saline treatment (CST) was evaluated on 160-day survival rate (53% reduction in relative risk ratio, p=0.002). Central intracerebroventricular microinfusion of donepezil significantly improved the 160-day survival rate compared to saline treatment (68% vs. 32%, P=0.002) in rats with chronic heart failure.
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