Dobutamine administration exacerbates postischaemic myocardial dysfunction in isolated rat hearts: an effect reversed by thyroxine pretreatment

Eur J Pharmacol. 2003 Jan 24;460(2-3):155-61. doi: 10.1016/s0014-2999(02)02927-8.

Abstract

The present study has investigated the effects of dobutamine on postischaemic dysfunction in the setting of global ischaemia and reperfusion in a model of isolated heart preparation. Isolated rat hearts were subjected to 20 min of zero-flow global ischaemia followed by 45 min of reperfusion. Dobutamine administration (10 microg/kg/min) during the reperfusion period resulted in deterioration of functional recovery, which was abolished by propranolol administration. Long-term thyroxine pretreatment (12.5 microg 100 g(-1) body weight, b.i.d., s.c., for 2 weeks) reversed the detrimental effect of dobutamine and increased postischaemic recovery of function. We conclude that the combination of thyroxine pretreatment and dobutamine administration could potentially be a new therapeutic strategy to improve postischaemic dysfunction particularly in clinical settings such as cardiopulmonary bypass and/or myocardial infarction.

MeSH terms

  • Animals
  • Cardiotonic Agents / adverse effects
  • Cardiotonic Agents / pharmacology*
  • Dobutamine / adverse effects
  • Dobutamine / pharmacology*
  • Heart / drug effects*
  • Heart / physiology
  • Heart / physiopathology
  • Heart Ventricles / drug effects
  • Heart Ventricles / physiopathology
  • In Vitro Techniques
  • Myocardial Ischemia / complications
  • Myocardial Reperfusion Injury / etiology
  • Myocardial Reperfusion Injury / physiopathology
  • Myocardial Reperfusion Injury / prevention & control*
  • Propranolol / pharmacology
  • Rats
  • Thyroxine / pharmacology*
  • Time Factors
  • Ventricular Function

Substances

  • Cardiotonic Agents
  • Dobutamine
  • Propranolol
  • Thyroxine