Reduction of myocardial infarct size by tetrahydrobiopterin: possible involvement of mitochondrial KATP channels activation through nitric oxide production

J Cardiovasc Pharmacol. 2006 Feb;47(2):243-9. doi: 10.1097/01.fjc.0000201360.71813.8a.

Abstract

This study examined whether intravenous administration of tetrahydrobiopterin (BH4) reduces myocardial infarct size following ischemia/reperfusion (I/R) in rats, and the mechanisms of its protective effect were also investigated. Rats were subjected to 30 minutes of ischemia by ligation of the left coronary artery and 2 hours of reperfusion. The infarct size was determined as a percentage of the area at risk by triphenyltetrazolium staining. Intravenous administration of BH4 (0.01 mg/kg-1 mg/kg) significantly reduced the myocardial infarct size. Nitrite plus nitrate (NOx) and cGMP levels in the hearts were significantly increased by the treatment with BH4, and the infarct size-limiting effect of BH4 was abolished by the co-administration of NG-nitro-L-arginine methyl ester, a specific inhibitor of nitric oxide synthase, or 5-hydroxydecanoic acid, a specific inhibitor of mitochondrial ATP-sensitive potassium channel (mitoKATP channel). These findings suggest that BH4 has a cardioprotective effect against I/R in vivo, and its protective effect appeared to be involved in the opening of mitoKATP channels through increased nitric oxide production.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Anti-Arrhythmia Agents / pharmacology
  • Arginine / pharmacology
  • Biopterins / administration & dosage
  • Biopterins / analogs & derivatives*
  • Biopterins / metabolism
  • Biopterins / pharmacology
  • Cyclic GMP / analysis
  • Decanoic Acids / pharmacology
  • Dose-Response Relationship, Drug
  • Enzyme Inhibitors / pharmacology
  • Hydroxy Acids / pharmacology
  • Male
  • Malondialdehyde / analysis
  • Myocardial Infarction / drug therapy*
  • Myocardial Infarction / etiology
  • Myocardial Infarction / pathology*
  • Myocardial Infarction / physiopathology
  • NG-Nitroarginine Methyl Ester / pharmacology
  • Nitrates / analysis
  • Nitric Oxide / biosynthesis*
  • Nitrites / analysis
  • Potassium Channels / drug effects
  • Potassium Channels / metabolism*
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Anti-Arrhythmia Agents
  • Decanoic Acids
  • Enzyme Inhibitors
  • Hydroxy Acids
  • Nitrates
  • Nitrites
  • Potassium Channels
  • mitochondrial K(ATP) channel
  • Biopterins
  • Nitric Oxide
  • Malondialdehyde
  • 5-hydroxydecanoic acid
  • Arginine
  • sapropterin
  • Cyclic GMP
  • NG-Nitroarginine Methyl Ester