Functional alterations in NO, PGI2 and EDHF pathways in the aortic endothelium after myocardial infarction in rats

Eur J Heart Fail. 2006 Dec;8(8):769-76. doi: 10.1016/j.ejheart.2006.09.011. Epub 2006 Nov 13.

Abstract

Background: Previous work on endothelial dysfunction in post-MI heart failure has shown conflicting results.

Aim: To analyze gender related alterations in NO-, PGI(2)- and EDHF-dependent endothelial function in the thoracic aorta 7 and 42 days after myocardial infarction (MI).

Methods and results: MI was induced by coronary artery ligation in female and male Sprague-Dawley rats. There was no gender related difference in infarct-size or in the impairment of fractional shortening of the left ventricle 42 days after coronary ligation. Neither acetylcholine-induced (Ach) vasodilation nor basal PGI(2) production in the aorta was modified by coronary ligation. Interestingly, 7 days after MI, basal NO production was impaired and the EDHF component of Ach-induced vasodilation was up-regulated, in both male and female rats. However, 42 days post-MI, basal NO was only impaired in male rats, while EDHF was only up-regulated in female rats.

Conclusion: MI induced impairment of functional activity of basal NO production and adaptive up-regulation of the EDHF component of Ach-induced relaxation. The above alterations in endothelial function in the aorta were gender-specific at 42 days but not 7 days after MI. Some of the previously reported discrepancies in the development of endothelial dysfunction in the post-MI period may be gender related differences.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Aorta / metabolism
  • Biological Factors / metabolism*
  • Cytochrome P-450 Enzyme System / metabolism
  • Endothelium / metabolism
  • Epoprostenol / metabolism*
  • Female
  • Male
  • Myocardial Infarction / metabolism*
  • Myocardial Infarction / physiopathology
  • Myocardial Infarction / surgery
  • Nitric Oxide / metabolism*
  • Potassium Channels / metabolism
  • Prostaglandin-Endoperoxide Synthases / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Up-Regulation
  • Ventricular Remodeling

Substances

  • Biological Factors
  • Potassium Channels
  • endothelium-dependent hyperpolarization factor
  • Nitric Oxide
  • Cytochrome P-450 Enzyme System
  • Epoprostenol
  • Prostaglandin-Endoperoxide Synthases