Dunye Guanxinning Improves Acute Myocardial Ischemia-Reperfusion Injury by Inhibiting Neutrophil Infiltration and

Q G Zhang1, S R Wang1, X M Chen1

  • 1Institute of Interdisciplinary Medical Science, Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China.

Insights

Dunye Guanxinning (DG) protects against heart attack damage by reducing inflammation and cell death. This traditional Chinese medicine works by inhibiting neutrophil infiltration and caspase-1 activity via the AMPK pathway.

Area of Science:

  • Cardiovascular Disease Research
  • Traditional Chinese Medicine Pharmacology
  • Inflammation and Immunity

Background:

  • Acute myocardial infarction (AMI) is a critical cardiovascular condition with significant mortality.
  • Dunye Guanxinning (DG), a traditional Chinese patent medicine, shows clinical efficacy in treating myocardial infarction.
  • The precise mechanism underlying DG's cardioprotective effects remains largely unelucidated.

Purpose of the Study:

  • To investigate the protective mechanism of Dunye Guanxinning (DG) in acute myocardial ischemia-reperfusion injury.
  • To test the hypothesis that DG inhibits neutrophil infiltration and caspase-1 activity.
  • To explore the role of the adenosine monophosphate-activated protein kinase (AMPK) pathway in DG's action.

Main Methods:

  • Administration of DG to rats subjected to myocardial ischemia-reperfusion injury.
  • Assessment of cardiac function, infarct size, and cardiomyocyte apoptosis.
  • Measurement of hemorheological parameters, oxidative stress markers, and inflammatory cytokines (IL-1β).
  • Evaluation of neutrophil infiltration, caspase-1 activity, and AMPK phosphorylation.

Main Results:

  • DG administration significantly reduced infarct size and cardiomyocyte apoptosis.
  • Improved cardiac function, including left ventricular ejection fraction and fractional shortening.
  • DG inhibited neutrophil infiltration, reduced serum IL-1β levels, and suppressed myocardial IL-1β maturation.
  • DG inhibited caspase-1 activity and promoted AMPK phosphorylation in the heart.

Conclusions:

  • DG demonstrates significant cardioprotective effects against ischemia-reperfusion injury in a rat model.
  • DG exerts its benefits by inhibiting inflammasome activity and IL-1β release, partly through the AMPK pathway.
  • These findings provide mechanistic insights supporting the clinical use of DG for myocardial infarction treatment.

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