Possible protective mechanisms exerted by metformin or metformin and vitamin E in isoproterenol-induced cardiac injury

J Cell Biochem. 2018 May;119(5):3903-3912. doi: 10.1002/jcb.26530. Epub 2018 Jan 23.

Abstract

Several studies have reported that metformin is cardioprotective for diabetic and non-diabetic ischemic hearts through mechanisms that cannot be entirely attributed to its anti-hyperglycemic effect. This study was designed to investigate the cardioprotective effects of metformin with and without vitamin E after induction myocardial infarction (MI) in rats, using isoproterenol. Administration of metformin or vitamin E significantly reduced the cardiac mass index (P < 0.01), ameliorated the changes to cardiac biomarkers, and attenuated oxidative stress levels compared to the isoproterenol group. Interestingly, combination therapy showed a slight synergistic effect. Histopathological analysis suggested that metformin treatment reduced NF-κB expression and protected against isoproterenol-induced MI. Our results indicate that metformin mediates a cardioprotective effect against isoproterenol-induced MI via antioxidant activity and modulation of the NF-κB signaling pathway. This suggests that metformin would be beneficial in MI treatment.

Keywords: NF κB; cardioprotection; metformin; myocardial infarction; oxidative stress; vitamin E.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Heart Injuries / chemically induced*
  • Heart Injuries / metabolism
  • Heart Injuries / pathology
  • Heart Injuries / prevention & control*
  • Isoproterenol / adverse effects*
  • Isoproterenol / pharmacology
  • Male
  • Metformin / pharmacology*
  • NF-kappa B / metabolism
  • Rats
  • Rats, Wistar
  • Signal Transduction / drug effects*
  • Vitamin E / pharmacology*

Substances

  • NF-kappa B
  • Vitamin E
  • Metformin
  • Isoproterenol