Erythropoietin Improves Cardiovascular Function in Adult Rats After Acute Hemorrhage

J Cardiovasc Pharmacol. 2019 May;73(5):290-300. doi: 10.1097/FJC.0000000000000666.

Abstract

Erythropoietin (EPO) has been linked to cardioprotective effects. However, its effects during the aging process are little known. We investigated the effect of EPO administration on hemodynamic parameters, cardiac function, oxidative damage, and erythropoietin receptor (EPOR) expression pattern in the hypovolemic state. EPO was administered (1000 IU/kg/3 days) and then acute hemorrhage (20% blood loss) was induced in young and adult rats. There was no difference in plasmatic EPO in either age group. The hemodynamic basal condition was similar, without alterations in renal function and hematocrit, in both age groups. After bleeding, both EPO-treated age groups had increased blood pressure at the end of the experimental protocol, being greater in adult animals. EPO attenuated the tachycardic effect. Ejection fraction and fractional shortening were higher in adult EPO-treated rats subjected to hemorrhage. In the left ventricle, young and adult EPO-treated rats subjected to bleeding showed an increased EPOR expression. A different EPOR expression pattern was observed in the adult right atrial tissue, compared with young animals. EPO treatment decreased oxidative damage to lipids in both age groups. EPO treatment before acute hemorrhage improves cardiovascular function during the aging process, which is mediated by different EPOR pattern expression in the heart tissue.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Age Factors
  • Animals
  • Cardiovascular System / drug effects*
  • Cardiovascular System / metabolism
  • Cardiovascular System / physiopathology
  • Disease Models, Animal
  • Epoetin Alfa / administration & dosage*
  • Hematinics / administration & dosage*
  • Hemodynamics / drug effects*
  • Hemorrhage / drug therapy*
  • Hemorrhage / metabolism
  • Hemorrhage / physiopathology
  • Lipid Peroxidation / drug effects
  • Male
  • Myocardium / metabolism
  • Oxidative Stress / drug effects
  • Rats, Sprague-Dawley
  • Receptors, Erythropoietin / agonists
  • Receptors, Erythropoietin / metabolism
  • Ventricular Function, Left / drug effects*

Substances

  • Hematinics
  • Receptors, Erythropoietin
  • Epoetin Alfa