Insulin/NFκB protects against ischemia-induced necrotic cardiomyocyte death

Biochem Biophys Res Commun. 2015 Nov 13;467(2):451-7. doi: 10.1016/j.bbrc.2015.09.171. Epub 2015 Oct 9.

Abstract

In the heart, insulin controls key functions such as metabolism, muscle contraction and cell death. However, all studies have been focused on insulin action during reperfusion. Here we explore the cardioprotective action of this hormone during ischemia. Rat hearts were perfused ex vivo with an ischemia/reperfusion Langendorff model in absence or presence of insulin. Additionally, cultured rat cardiomyocytes were exposed to simulated ischemia in the absence or presence of insulin. Cytoprotective effects were measured by myocardial infarct size, trypan blue exclusion, released LDH and DNA fragmentation by flow cytometry. We found that insulin protected against cardiac ischemia ex vivo and in vitro. Moreover, insulin protected cardiomyocytes from simulated ischemia by reducing necrotic cell death. Protective effects of insulin were dependent of Akt and NFκB. These novel results show that insulin reduces ischemia-induced cardiomyocyte necrosis through an Akt/NF-κB dependent mechanism. These novel findings clarify the role of insulin during ischemia and further support its use in early GIK perfusion to treat myocardial infarction.

Keywords: Cell death; Cell signaling; Heart; Insulin; Ischemia.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cardiotonic Agents / pharmacology*
  • DNA Fragmentation / drug effects
  • Gene Expression
  • Heart / drug effects
  • Heart / physiopathology
  • Insulin / pharmacology*
  • L-Lactate Dehydrogenase / metabolism
  • Myocardial Infarction / genetics
  • Myocardial Infarction / metabolism
  • Myocardial Infarction / pathology
  • Myocardial Infarction / prevention & control*
  • Myocardial Reperfusion Injury / genetics
  • Myocardial Reperfusion Injury / metabolism
  • Myocardial Reperfusion Injury / pathology
  • Myocardial Reperfusion Injury / prevention & control*
  • Myocytes, Cardiac / drug effects
  • Myocytes, Cardiac / metabolism
  • Myocytes, Cardiac / pathology
  • NF-kappa B / genetics
  • NF-kappa B / metabolism*
  • Necrosis / genetics
  • Necrosis / metabolism
  • Necrosis / pathology
  • Necrosis / prevention & control*
  • Organ Culture Techniques
  • Primary Cell Culture
  • Proto-Oncogene Proteins c-akt / genetics
  • Proto-Oncogene Proteins c-akt / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Signal Transduction

Substances

  • Cardiotonic Agents
  • Insulin
  • NF-kappa B
  • L-Lactate Dehydrogenase
  • Proto-Oncogene Proteins c-akt