S-allylcysteine ameliorates isoproterenol-induced cardiac toxicity in rats by stabilizing cardiac mitochondrial and lysosomal enzymes

Life Sci. 2007 Feb 13;80(10):972-8. doi: 10.1016/j.lfs.2006.11.028. Epub 2006 Nov 23.

Abstract

This study was aimed to evaluate the preventive role of S-allylcysteine (SAC) on mitochondrial and lysosomal enzymes in isoproterenol (ISO)-induced rats. Male albino Wistar rats were pretreated with SAC (50, 100 and 150 mg/kg) daily for a period of 45 days. After the treatment period, ISO (150 mg/kg) was subcutaneously injected to rats at an interval of 24 h for two days. The activities of heart mitochondrial enzymes (isocitrate dehydrogenase, succinate dehydrogenase, malate dehydrogenase and alpha-ketoglutarate dehydrogenase) and respiratory chain enzymes (NADH dehydrogenase and cytochrome C oxidase) were decreased significantly (p<0.05) in ISO-induced rats. The activities of lysosomal enzymes (beta-glucuronidase, beta-N-acetyl glucosaminidase, beta-galactosidase, cathepsin-D and acid phosphatase) were increased significantly (p<0.05) in serum and heart of ISO-induced rats. Pretreatment with SAC (100 mg/kg and 150 mg/kg) for a period of 45 days increased significantly (p<0.05) the activities of mitochondrial and respiratory chain enzymes and decreased the activities of lysosomal enzymes significantly (p<0.05) in ISO-induced rats. Oral administration of SAC (50, 100 and 150 mg/kg) for a period of 45 days to normal rats did not show any significant (p<0.05) effect in all the parameters studied. The altered electrocardiogram (ECG) of ISO-treated rats was also restored to near normal by treatment with SAC (100 and 150 mg/kg). These results confirm the efficacy of SAC in alleviating ISO-induced cardiac damage.

MeSH terms

  • Adrenergic beta-Agonists / pharmacology*
  • Animals
  • Antineoplastic Agents / pharmacology*
  • Cysteine / analogs & derivatives*
  • Cysteine / pharmacology
  • Electrocardiography
  • Heart Diseases / chemically induced
  • Heart Diseases / prevention & control*
  • Isoproterenol / antagonists & inhibitors
  • Isoproterenol / toxicity*
  • Lysosomes / drug effects
  • Lysosomes / enzymology*
  • Male
  • Mitochondria, Heart / drug effects
  • Mitochondria, Heart / enzymology*
  • Myocardial Infarction / chemically induced
  • Myocardial Infarction / pathology
  • Rats
  • Rats, Wistar
  • Thiobarbituric Acid Reactive Substances / metabolism
  • alpha-Tocopherol / pharmacology

Substances

  • Adrenergic beta-Agonists
  • Antineoplastic Agents
  • Thiobarbituric Acid Reactive Substances
  • S-allylcysteine
  • alpha-Tocopherol
  • Cysteine
  • Isoproterenol