Abstract

BackgroundWe have previously demonstrated that the chronic intervention in the cholinergic system by donepezil, an acetylcholinesterase inhibitor, plays a beneficial role in suppressing long-term cardiac remodeling after myocardial infarction (MI). In comparison with such a chronic effect, however, the acute effect of donepezil during an acute phase of MI remains unclear. Noticing recent findings of a cholinergic mechanism for anti-inflammatory actions, we tested the hypothesis that donepezil attenuates an acute inflammatory tissue injury following MI.Methods and ResultsIn isolated and activated macrophages, donepezil significantly reduced intra- and extracellular matrix metalloproteinase-9 (MMP-9). In mice with MI, despite the comparable values of heart rate and blood pressure, the donepezil-treated group showed a significantly lower incidence of cardiac rupture than the untreated group during the acute phase of MI. Immunohistochemistry revealed that MMP-9 was localized at the infarct area where a large number of inflammatory cells including macrophages infiltrated, and the expression and the enzymatic activity of MMP-9 at the left ventricular infarct area was significantly reduced in the donepezil-treated group.ConclusionThe present study suggests that donepezil inhibits the MMP-9-related acute inflammatory tissue injury in the infarcted myocardium, thereby reduces the risk of left ventricular free wall rupture during the acute phase of MI.

Highlights

  • The present study suggests that donepezil inhibits the matrix metalloproteinase-9 (MMP-9)-related acute inflammatory tissue injury in the infarcted myocardium, thereby reduces the risk of left ventricular free wall rupture during the acute phase of myocardial infarction (MI)

  • Effect of donepezil on macrophage matrix metalloproteinases (MMPs)-9 Compared to the control, lipopolysaccaride (LPS) treatment at a concentration of 10 ng/ml for 3 hrs significantly increased macrophage matrix metalloproteinase-9 (MMP-9) secretion to culture medium (LPS, 116.166 5.37% versus control, n = 11, P,0.01)

  • These results indicate that the inhibitory effect of donepezil on macrophage MMP-9 is independent of ACh

Read more

Summary

Introduction

Donepezil has been shown to 1) prevent cardiac remodeling with enhancing vagal activity in a rat chronic MI model [13], 2) improve survival by preventing pumping failure in a mouse volume overload model [14] and 3) up-regulate angiogenesis by modulating angiogenesis-responsible machinery of endothelial cells in a mouse ischemic hindlimb model [15], indicating that the donepezil possesses neuroprotective but cardioprotective effects. In comparison with such chronic effects, the acute effect of donepezil during an acute phase of MI remains unclear. Noticing recent findings of a cholinergic mechanism for anti-inflammatory actions, we tested the hypothesis that donepezil attenuates an acute inflammatory tissue injury following MI

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call