Effects of caffeic acid phenethyl ester on isoproterenol-induced myocardial infarction in rats

Anadolu Kardiyol Derg. 2010 Aug;10(4):298-302. doi: 10.5152/akd.2010.086.

Abstract

Objective: Caffeic acid phenethyl ester (CAPE) is a natural product with potent anti-inflammatory, antitumor and antioxidant activities and attenuates inflammation and lipid peroxidation induced by ischemia-reperfusion injury. The purpose of the present study was to investigate the effects of CAPE on isoproterenol (ISO) -induced myocardial infarction.

Methods: A randomized controlled experimental design was used in this study. Rats were divided into four groups and treated with saline, CAPE, ISO and ISO+CAPE. Rats were treated with CAPE (10 micromol kg/day i.p.) or saline starting 3 days before injecting ISO (150 mg /kg s.c., 24 hours). Seven days later, rats were sacrificed and the hearts were excised for biochemical analyses and microscopic examination. One-way ANOVA test with post hoc multiple comparisons using LSD method were used for statistical analysis of the data.

Results: The administration of ISO alone resulted in higher myeloperoxidase (MPO) activity, lipid peroxidation, superoxide dismutase (SOD) and catalase (CAT) than in the control. The enzyme activities did not change in rat given CAPE alone. CAPE treatment prevented the increase in MPO activity and malondialdehyde, but did not affect the activities SOD and CAT enzymes.

Conclusion: In light of these results, we conclude that CAPE prevents MPO-and lipid peroxidation-mediated myocardial injury via inhibition of neutrophil's MPO activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenergic beta-Antagonists / pharmacology
  • Animals
  • Aspartate Aminotransferases / blood
  • Caffeic Acids / therapeutic use*
  • Cardiotonic Agents / pharmacology*
  • Creatine Kinase / blood
  • Cytotoxins / pharmacology
  • Female
  • Flavonoids / therapeutic use
  • Humans
  • Isoproterenol / pharmacology*
  • L-Lactate Dehydrogenase / blood
  • Myocardial Infarction / chemically induced*
  • Peroxidase / metabolism
  • Phenylethyl Alcohol / analogs & derivatives*
  • Phenylethyl Alcohol / therapeutic use
  • Randomized Controlled Trials as Topic
  • Rats
  • Rats, Wistar
  • Superoxide Dismutase / metabolism

Substances

  • Adrenergic beta-Antagonists
  • Caffeic Acids
  • Cardiotonic Agents
  • Cytotoxins
  • Flavonoids
  • L-Lactate Dehydrogenase
  • Peroxidase
  • Superoxide Dismutase
  • Aspartate Aminotransferases
  • Creatine Kinase
  • caffeic acid phenethyl ester
  • Isoproterenol
  • Phenylethyl Alcohol