Experimental study of the relationship between perfluoro-octyl bromide emulsion and norepinephrine release in reperfusion arrhythmia: isolated guinea pig heart model

Ann Thorac Cardiovasc Surg. 2008 Dec;14(6):363-8.

Abstract

Background: Perfluoro-octyl bromide (PFOB), one of the perfluorochemical oxygen transporters, improved postischemic cardiac dysfunctions. Also norepinephrine (NE) is one of the important inducible factors on reperfusion arrhythmias (ventricular fibrillation [VF]). We used these methods to evaluate the relationship between PFOB emulsion and NE release on reperfusion arrhythmias.

Materials and methods: The perfusion of isolated guinea pig hearts was employed: each of four groups of 6-7 hearts were used with Krebs-Henseleit solution (KHS) as control, and KHS with 5%, 15%, or 30% PFOB emulsion. The hearts were perfused in a constant pressure Langendorff model, stabilized for 30 min, followed by 30 min preischemia, then 30 min ischemia and 45 min reperfusion at normothermia.

Results: PFOB emulsion dose-dependently limited VF and inhibited NE release in reperfusion. Only 30% PFOB emulsion showed the significant improvement of VF (p=0.05). In hemodynamic parameters, only 5% PFOB emulsion showed a significant decrease in reperfusion, but there was no difference in coronary flow rate (CFR). No differences among the four groups were demonstrated in cardiac oxygen metabolic parameters.

Conclusions: It was most likely that a high concentration of PFOB emulsion attenuated reperfusion arrhythmia by decreasing NE release.

MeSH terms

  • Animals
  • Blood Substitutes / pharmacology*
  • Coronary Circulation / drug effects
  • Dose-Response Relationship, Drug
  • Emulsions
  • Fluorocarbons / pharmacology*
  • Guinea Pigs
  • Heart Rate / drug effects
  • Hydrocarbons, Brominated
  • In Vitro Techniques
  • Male
  • Myocardial Reperfusion Injury / complications
  • Myocardial Reperfusion Injury / drug therapy*
  • Myocardial Reperfusion Injury / metabolism
  • Myocardial Reperfusion Injury / physiopathology
  • Myocardium / metabolism*
  • Norepinephrine / metabolism*
  • Oxygen Consumption / drug effects
  • Perfusion
  • Ventricular Fibrillation / etiology
  • Ventricular Fibrillation / metabolism
  • Ventricular Fibrillation / physiopathology
  • Ventricular Fibrillation / prevention & control*
  • Ventricular Function, Left / drug effects
  • Ventricular Pressure / drug effects

Substances

  • Blood Substitutes
  • Emulsions
  • Fluorocarbons
  • Hydrocarbons, Brominated
  • perflubron
  • Norepinephrine