2,6-Diisobornyl-4-Methylphenol Reduces Postishemic Myocardium Remodeling in Delayed Period after Ischemia/Reperfusion in Rats

Bull Exp Biol Med. 2020 Jul;169(3):310-313. doi: 10.1007/s10517-020-04876-9. Epub 2020 Aug 3.

Abstract

2,6-Diisobornyl-4-methylphenol (Dibornol, 10 mg/kg intragastrically daily for 5 days after myocardial ischemia/reperfusion) 1.5-fold increased rat survival during the acute post-infarction period in comparison with the control group. In survivors, Dibornol reliably prevented post-ischemic progression of heart failure in the delayed post-infarction period (30 days after ischemia/reperfusion), which was seen from an increase in the left-ventricular developed pressure by 22%, left-ventricular contractility index by 19%, and +dP/dt by 34%. Left-ventricular end-diastolic pressure was by 39% lower than in control animals. Morphological study of heart sections from control group animals showed that Dibornol reduced the area of post-ischemic myocardial damage in the delayed period after ischemia/reperfusion to 3±1% (vs 18±2% in the control group).

Keywords: 2,6-diisobornyl-4-methylphenol; cardiac contractile function; myocardial ischemia/reperfusion; post-ischemic myocardial damage; rats.

MeSH terms

  • Animals
  • Blood Pressure / drug effects
  • Cresols / chemistry
  • Cresols / therapeutic use*
  • Heart / drug effects
  • Heart Ventricles / drug effects*
  • Heart Ventricles / metabolism
  • Male
  • Myocardial Reperfusion
  • Myocardial Reperfusion Injury / drug therapy*
  • Myocardial Reperfusion Injury / metabolism
  • Rats

Substances

  • Cresols
  • cresol