Protective effects of thymol on altered plasma lipid peroxidation and nonenzymic antioxidants in isoproterenol-induced myocardial infarcted rats

J Biochem Mol Toxicol. 2012 Sep;26(9):368-73. doi: 10.1002/jbt.21431. Epub 2012 Aug 13.

Abstract

This study evaluates the protective effects of thymol on altered plasma lipid peroxidation products and nonenzymic antioxidants in isoproterenol (ISO)-induced myocardial infarcted rats. Male albino Wistar rats were pre and cotreated with thymol (7.5 mg/kg body weight) daily for 7 days. ISO (100 mg/kg body weight) was subcutaneously injected into rats on 6th and 7th day to induce myocardial infarction (MI). Increased activity/levels of serum creatine kinase-MB (CK-MB), plasma thiobarbituric acid reactive substances, lipid hydroperoxides, and conjugated dienes with decreased levels of plasma reduced glutathione (GSH), vitamin C, and vitamin E were observed in ISO-induced myocardial infarcted rats. Pre and cotreatment with thymol (7.5 mg/kg body weight) showed normalized activity of serum CK-MB and near normalized levels of plasma lipid peroxidation products, reduced GSH, vitamin C, and vitamin E in myocardial infarcted rats. Furthermore, the in vitro study on reducing power of thymol confirmed its potent antioxidant action. Thus, thymol protects ISO-induced MI in rats by its antilipid peroxidation and antioxidant properties.

MeSH terms

  • Animals
  • Antioxidants / metabolism*
  • Cardiotonic Agents / pharmacology*
  • Cardiotonic Agents / therapeutic use
  • Creatine Kinase, MB Form / blood
  • Dose-Response Relationship, Drug
  • Glutathione / blood
  • Isoproterenol
  • Lipid Peroxidation*
  • Male
  • Myocardial Infarction / blood
  • Myocardial Infarction / chemically induced
  • Myocardial Infarction / drug therapy*
  • Rats
  • Rats, Wistar
  • Reducing Agents / pharmacology
  • Reducing Agents / therapeutic use
  • Thiobarbituric Acid Reactive Substances / metabolism
  • Thymol / pharmacology*
  • Thymol / therapeutic use

Substances

  • Antioxidants
  • Cardiotonic Agents
  • Reducing Agents
  • Thiobarbituric Acid Reactive Substances
  • Thymol
  • Creatine Kinase, MB Form
  • Glutathione
  • Isoproterenol