Department of Cardiovascular Dynamics, National Cerebral and Cardiovascular Center, Osaka, Japan.
J Physiol Sci. 2020 Feb 17;70(1):11. doi: 10.1186/s12576-020-00739-0.
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.
口服多奈哌齐,一种中枢作用的乙酰胆碱酯酶抑制剂,可改善慢性心力衰竭(CHF)大鼠的生存率。然而,多奈哌齐的心脏保护作用机制仍完全不清楚。为了阐明潜在的机制,我们研究了多奈哌齐的中枢微输注是否会发挥心脏保护作用。在心肌梗死大鼠中植入带有脑室套管的脑室内微输注泵。大鼠被随机分为中央生理盐水处理(CST)和中央多奈哌齐处理(CDT)组。我们在 6 周治疗后评估了心脏重构和功能,并检查了 160 天的存活率。与 CST 相比,CDT 通过预防心脏重构和降低血浆儿茶酚胺、脑利钠肽和血管紧张素 II,显著提高了 160 天的存活率(68%对 32%,P=0.002)。这些结果表明,中枢机制在多奈哌齐的心脏保护作用中发挥重要作用。