Sinapic acid safeguards cardiac mitochondria from damage in isoproterenol-induced myocardial infarcted rats

J Biochem Mol Toxicol. 2020 Oct;34(10):e22556. doi: 10.1002/jbt.22556. Epub 2020 Jul 5.

Abstract

Myocardial infarction (MI) is a life-threatening disease. In this study, we examined the anti-mitochondrial damaging effects of sinapic acid (SA) in isoproterenol (ISO)-induced myocardial infarcted rats. Myocardial infarcted rats were prepared by injecting ISO (100 mg/kg body weight) on the 9th and 10th day. Rats were pretreated and cotreated with SA (12 mg/kg body weight) orally, daily for 10 days. A considerable increase in serum lactate dehydrogenase, creatine kinase, myoglobin, and cardiac troponin-T was noticed in the ISO-induced rats. ISO also significantly amplified lipid peroxidation and calcium ions, and depleted the antioxidant system and mitochondrial enzymes in rat's heart mitochondria. SA treatment improved the distorted above- mentioned biochemical parameters in ISO-treated rats with its anti-mitochondrial damaging effects. This ultrastructural study on heart mitochondria and in vitro studies also confirmed the effects of SA. The current findings are suggestive of SA's cardioprotective effects.

Keywords: antioxidants; mitochondrial damage; myocardial infarction; myoglobin; sinapic acid.

MeSH terms

  • Adrenergic beta-Agonists / toxicity*
  • Animals
  • Biomarkers / blood
  • Cardiotonic Agents / pharmacology*
  • Coumaric Acids / pharmacology*
  • Isoproterenol / toxicity*
  • Male
  • Mitochondria, Heart / drug effects*
  • Mitochondria, Heart / ultrastructure
  • Myocardial Infarction / chemically induced
  • Myocardial Infarction / pathology*
  • Oxidative Stress / drug effects
  • Rats
  • Rats, Wistar

Substances

  • Adrenergic beta-Agonists
  • Biomarkers
  • Cardiotonic Agents
  • Coumaric Acids
  • sinapinic acid
  • Isoproterenol