Cardioprotective effects of glucose and insulin administration while maintaining normoglycemia (GIN therapy) in patients undergoing coronary artery bypass grafting

J Clin Endocrinol Metab. 2011 May;96(5):1469-77. doi: 10.1210/jc.2010-1934. Epub 2011 Feb 23.

Abstract

Context: Coronary artery bypass grafting (CABG) is complicated by ischemia-reperfusion injury jeopardizing myocyte survival.

Objective: The aim of the study was to investigate whether glucose and insulin administration, while maintaining normoglycemia (GIN therapy) using a hyperinsulinemic-normoglycemic clamp technique, is cardioprotective in patients undergoing CABG.

Design and setting: We conducted a randomized controlled trial at a tertiary care university teaching hospital.

Patients: We studied 99 patients undergoing elective CABG.

Intervention: Patients were randomly assigned to receive either GIN from the beginning of surgery until 24 h after CABG (GIN, n = 49) or standard metabolic care (control, n = 50).

Main outcome measures: We measured plasma concentrations of cardiac troponin I and free fatty acids, cardiac function as assessed by transesophageal echocardiography, glycogen content, glycogen synthase activity, and the expression of AMP-activated protein kinase (AMPK) and protein kinase B (AKT) in cardiomyocytes.

Results: Patients receiving GIN therapy showed an attenuated release of cardiac troponin I (P < 0.05) and improved myocardial function (P < 0.05). Systemic free fatty acid concentrations were suppressed (P < 0.05), whereas intracellular glycogen content and glycogen synthase activity were not altered. The AMPK activity remained unchanged during ischemia in the GIN group, whereas it increased in the control group (P < 0.05). Enhanced AKT phosphorylation before ischemia was observed (P < 0.05) in the presence of GIN. However, there was no evidence for AKT-dependent AMPK inhibition.

Conclusions: GIN therapy protects the myocardium and inhibits ischemia-induced AMPK activation.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Anesthesia
  • Biopsy
  • Blood Glucose / metabolism*
  • Cardiotonic Agents*
  • Coronary Artery Bypass / adverse effects*
  • Cyclic AMP-Dependent Protein Kinases / metabolism
  • Echocardiography
  • Energy Metabolism / physiology
  • Female
  • Glucose / therapeutic use*
  • Glucose Clamp Technique
  • Glycogen / metabolism
  • Glycogen Synthase / metabolism
  • Humans
  • Hypoglycemic Agents / therapeutic use*
  • Insulin / therapeutic use*
  • Male
  • Middle Aged
  • Muscle, Skeletal / pathology
  • Myocardial Reperfusion Injury / prevention & control
  • Myocardial Revascularization
  • Oncogene Protein v-akt / metabolism
  • Postoperative Complications / prevention & control
  • Treatment Outcome
  • Troponin C / blood

Substances

  • Blood Glucose
  • Cardiotonic Agents
  • Hypoglycemic Agents
  • Insulin
  • Troponin C
  • Glycogen
  • Glycogen Synthase
  • Oncogene Protein v-akt
  • Cyclic AMP-Dependent Protein Kinases
  • Glucose