A novel hemoglobin-based blood substitute protects against myocardial reperfusion injury

• Published in: American journal of physiology. Heart and circulatory physiology 2005-04, Vol.288 (4), p.H1796-H1801
• Main Authors: Caswell, John E, Strange, Micah B, Rimmer, David M., III, Gibson, Michael F, Cole, Phillip, Lefer, David J
• Format: Article
• Language: English
• Subjects: Animals; Blood Pressure; Blood Substitutes - pharmacology; Coronary Circulation - drug effects; Creatine Kinase - metabolism; Creatine Kinase, MB Form; Dogs; Female; Heart Rate; Hemoglobins - pharmacology; Isoenzymes - metabolism; Leukocyte Count; Male; Myocardial Infarction - drug therapy; Myocardial Infarction - pathology; Myocardial Reperfusion Injury - drug therapy; Myocardial Reperfusion Injury - pathology; Neutrophils - cytology; Platelet Count; Ventricular Pressure
• ISSN: 0363-6135; 1522-1539
• DOI: 10.1152/ajpheart.00905.2004

Departments of 1 Molecular and Cellular Physiology and 2 Surgery, Louisiana State University Health Sciences Center, Shreveport, Louisiana Submitted 31 August 2004 ; accepted in final form 24 November 2004 HBOC-201 (Biopure; Cambridge, MA) is a glutaraldehyde-polymerized bovine hemoglobin (Hb) solution that is stroma free, has lower viscosity than blood, and promotes O 2 unloading. We investigated the effects of HBOC-201 in a canine model of myocardial ischemia-reperfusion injury. Dogs were anesthetized and subjected to 90 min of regional myocardial ischemia and 270 min of reperfusion. HBOC-201 or 0.9% saline vehicle equivalent to 10% total blood volume was infused 30 min before myocardial ischemia. Hemodynamic data and peripheral blood samples were taken at baseline, 1 h of myocardial ischemia, and 1, 2, and 4 h of reperfusion. At 270 min of reperfusion, the area at risk (AAR) per left ventricle and the area of infarction (Inf) per AAR were determined. The myocardial AARs in the two study groups were similar. In addition, myocardial blood flow (as measured by radioactive microspheres) in the ischemic zone was similar between the vehicle and HBOC-201 groups. HBOC-201-infused dogs demonstrated a significant ( P < 0.01) 56% reduction in Inf/AAR. Analysis of blood samples taken at 4 h of reperfusion showed a significant ( P < 0.05) reduction in creatine kinase MB isoform for the HBOC-201 group. Histological analysis of the myocardium demonstrated significant ( P < 0.01) reductions in neutrophil infiltration in the HBOC-201 group. These data indicate that treatment with HBOC-201 before myocardial ischemia-reperfusion reduces the extent of myocardial inflammation and ischemia-reperfusion injury in the canine myocardium. infarction; contractility; neutrophils; ischemia Address for reprint requests and other correspondence: D. J. Lefer, Dept. of Molecular and Cellular Physiology, LSU Health Sciences Center, 1501 Kings Hwy., Shreveport, LA 71130 (E-mail: dlefer{at}lsuhsc.edu )