Protective effects of the standardized extract of Zingiber officinale on myocardium against isoproterenol-induced biochemical and histopathological alterations in rats

Pharm Biol. 2015;53(12):1795-802. doi: 10.3109/13880209.2015.1008147. Epub 2015 Apr 14.

Abstract

Context: Ginger [Zingiber officinale Roscoe. (Zingiberaceae)] has been universally used as a spice as well as for its health benefits.

Objective: The present study evaluates the protective effect of the standardized extract of ginger against isoproterenol (ISO)-induced myocardial infarction (MI) in rats.

Materials and methods: Wistar rats were pretreated orally with three doses of standardized ginger extract (100, 200, and 400 mg/kg of body weight) or propranolol (5 mg/mL) for 28 d prior to ISO (85 mg/kg) induced MI in two doses on days 29 and 30. The rats were sacrificed 48 h after the first induction; serum and hearts were collected for biochemical and histopathological analysis.

Results: Gingerols and shogaols were identified and quantitatively analyzed in the extracts using validated reversed phase HPLC methods. Pretreatment with ginger extract at 400 mg/kg showed a significant decrease (p < 0.05) in all the cardiac enzyme activities, i.e., cardiac troponin I (cTnI) (0.57 ng/mL), creatine kinase MB isoenzyme (CK-MB) (10.34 pg/mL), lactate dehydrogenase (LDH) (115.22 U/L), alanine transaminase (ALT) (15.79 U/L), and aspartate transaminase (AST) (46.72 U/L) when compared with ISO-control rats. There were significant rises (p < 0.05) in the activity of glutathione peroxide (GPx) (53.16 U/L), catalase (CAT) (210.41 U/L), and superoxide dismutase (SOD) (280.89 U/mL) of the pretreated rats when compared with the ISO-control. Histopathological examination showed an improvement in membrane cell integrity in pretreated rats compared with untreated rats.

Conclusion: The ethanol extract of ginger exhibited cardioprotective potential in treating myocardial injury following ISO administration.

Keywords: Cardioprotective effect; gingerols; myocardial infarction; oxidative stress; serum marker enzymes; shogaols.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cardiotonic Agents / isolation & purification
  • Cardiotonic Agents / pharmacology
  • Cardiotonic Agents / therapeutic use*
  • Dose-Response Relationship, Drug
  • Isoproterenol / toxicity*
  • Male
  • Myocardial Infarction / chemically induced
  • Myocardial Infarction / pathology*
  • Myocardial Infarction / prevention & control*
  • Myocardium / pathology
  • Plant Extracts / isolation & purification
  • Plant Extracts / therapeutic use*
  • Rats
  • Rats, Wistar
  • Zingiber officinale*

Substances

  • Cardiotonic Agents
  • Plant Extracts
  • Isoproterenol