Caloric restriction attenuates aging-induced cardiac insulin resistance in male Wistar rats through activation of PI3K/Akt pathway

Nutr Metab Cardiovasc Dis. 2019 Jan;29(1):97-105. doi: 10.1016/j.numecd.2018.09.005. Epub 2018 Sep 26.

Abstract

Background and aim: Caloric restriction (CR) improves insulin sensitivity and is one of the dietetic strategies most commonly used to enlarge life and to prevent aging-induced cardiovascular alterations. The aim of this study was to analyze the possible beneficial effects of caloric restriction (CR) preventing the aging-induced insulin resistance in the heart of male Wistar rats.

Methods and results: Three experimental groups were used: 3 months old rats (3m), 24 months old rats (24m) and 24 months old rats subjected to 20% CR during their three last months of life (24m-CR). After sacrifice hearts were mounted in a perfusion system (Langendorff) and heart function in basal conditions and in response to accumulative doses of insulin (10-9-10-7 M), in the presence or absence of Wortmannin (10-6 M), was recorded. CR did not attenuate the aging-induced decrease in coronary artery vasodilation in response to insulin administration, but it prevented the aging-induced downregulation of cardiac contractility (dp/dt) through activation of the PI3K/Akt intracellular pathway. Insulin stimulated in a greater extent the PI3K/Akt pathway vs the activation of the MAPK pathway and increased the protein expression of IR, GLUT-4 and eNOS in the hearts of 3m and 24m-CR rats, but not in the hearts of 24m rats. Furthermore, CR prevented the aging induced increase in endothelin-1 protein expression in myocardial tissue.

Conclusion: In conclusion CR partially improves cardiac insulin sensitivity and prevents the aging induced decrease in myocardial contractility in response to insulin administration through activation of PI3K/Akt pathway.

Keywords: Aging; Akt; Caloric restriction; Cardiovascular; Heart; Insulin; Langendorff; Rat.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Age Factors
  • Aging
  • Animal Nutritional Physiological Phenomena
  • Animals
  • Caloric Restriction*
  • Coronary Vessels / drug effects
  • Coronary Vessels / enzymology
  • Coronary Vessels / physiopathology
  • Disease Models, Animal
  • Endothelin-1 / metabolism
  • Glucose Transporter Type 4 / metabolism
  • Heart / drug effects*
  • Heart / physiopathology
  • Insulin / pharmacology*
  • Insulin Resistance*
  • Isolated Heart Preparation
  • Male
  • Myocardial Contraction / drug effects
  • Myocardium / enzymology*
  • Nitric Oxide Synthase Type III / metabolism
  • Phosphatidylinositol 3-Kinase / metabolism*
  • Proto-Oncogene Proteins c-akt / metabolism*
  • Rats, Wistar
  • Signal Transduction / drug effects
  • Vasodilation / drug effects

Substances

  • Endothelin-1
  • Glucose Transporter Type 4
  • Insulin
  • Slc2a4 protein, rat
  • Nitric Oxide Synthase Type III
  • Nos3 protein, rat
  • Phosphatidylinositol 3-Kinase
  • Proto-Oncogene Proteins c-akt