Cardioprotective effects of tetrahydrobiopterin in cold heart preservation after cardiac arrest

Ann Thorac Cardiovasc Surg. 2006 Apr;12(2):95-104.

Abstract

Background: It has recently been shown that tetrahydrobiopterin (BH4), an essential cofactor of nitric oxide synthase (NOS), reduces ischemia-reperfusion myocardial injury. The aim of this study was to determine if supplementation with BH4 after cardiac arrest followed by cold heart preservation would exert a cardioprotective effect against ischemia-reperfusion injury.

Materials and methods: Isolated perfused rat hearts were subjected to 4 degrees C cold ischemia and reperfusion. Hearts were treated with cold cardioplegic solution with or without BH4 just before ischemia and during the first 5 min of reperfusion period. Effects of BH4 on left ventricular function, myocardial contents of high-energy phosphates, and nitrite plus nitrate were measured in the perfusate, before ischemia and after reperfusion. Moreover, the effect of BH4 on the cold-heart preservation followed by normothermic (37 degrees C) ischemia was determined.

Results: BH4 improved the contractile and metabolic abnormalities in reperfused cold preserved hearts that were subjected to normothermic ischemia. Furthermore, BH4 significantly alleviated ischemic contracture during ischemia, and restored the diminished perfusate levels of nitrite plus nitrate after reperfusion.

Conclusion: These results demonstrated that BH4 reduces ischemia-reperfusion injury in cold heart preservation. The cardioprotective effect of BH4 implies that BH4 could be a novel and effective therapeutic option in the preservation treatment of donor heart after cardiac arrest.

MeSH terms

  • Animals
  • Biopterins / analogs & derivatives*
  • Biopterins / metabolism
  • Biopterins / pharmacology
  • Cardiotonic Agents / metabolism
  • Cardiotonic Agents / pharmacology*
  • Cold Ischemia*
  • Disease Models, Animal
  • Heart Arrest / drug therapy
  • Heart Arrest / enzymology
  • Heart Transplantation
  • Heart Ventricles / drug effects*
  • Male
  • Myocardial Reperfusion Injury / enzymology
  • Myocardial Reperfusion Injury / prevention & control*
  • Myocardium / metabolism
  • Myocardium / pathology
  • Nitric Oxide Synthase / metabolism
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Cardiotonic Agents
  • Biopterins
  • Nitric Oxide Synthase
  • sapropterin