Experimental Cardiomyopathy as a Model of Chronic Heart Failure

• Published in: Journal of investigative surgery 1997, Vol.10 (6), p.387-396
• Main Authors: Shah, Himansu R., Vaynblat, Mikhail, Ramdev, Geeta, Cunningham, Joseph N., Chiavarelli, Mario
• Format: Article
• Language: English
• Subjects: Animals; Biological Transport; Cardiac Output, Low - chemically induced; Cardiomyopathies - chemically induced; cardiomyopathy; Disease Models, Animal; Dogs; Dose-Response Relationship, Drug; doxorubicin; Doxorubicin - toxicity; Echocardiography; experimental heart failure; Hemodynamics - drug effects; Infusions, Intravenous; Male; Monitoring, Physiologic - methods; Oxygen - pharmacokinetics; Survival Rate
• ISSN: 0894-1939; 1521-0553
• DOI: 10.3109/08941939709099603

End-stage heart disease is a major health care issue and it represents one of the most costly diseases. Several experimental heart failure models have been developed; however, a single model is not widely accepted as representative of clinical heart failure. The doxorubicin-induced cardiomyopathy model was used in the current study to address two issues: 1) to define a standardized dose regimen of intracoronary doxorubicin infusion; and 2) to establish a method of determining the onset and time course of heart failure. Twenty dogs underwent placement of an intracoronary catheter. A total dose of 1 mg/kg of intracoronary doxorubicin was infused. Hemodynamics were obtained at weeks 0, 7, and 12. Echocardiography was performed weekly. Right and left ventricular biopsy specimens were examined at weeks 0 and 12. Survival after doxorubicin-induced cardiomyopathy was 60% at week 12. The development of heart failure was demonstrated by a significant decrease in left ventricular ejection fraction and cardiac index and a significant increase in left ventricular end-diastolic pressure and volume. The leukocyte count, hemoglobin, and hematocrit decreased significantly. Histologic changes of both the right and left ventricular myocardial biopsy specimens included myocellular hypertrophy, loss of myofibrillar material, and vacuolization. Intracoronary doxorubicin reliably produced an experimental model of accelerated heart failure that developed over the course of 12 weeks. Echocardiographic monitoring allowed a close surveillance of heart failure development. This model may be useful to evaluate the efficacy of cardiomyoplasty, mechanical assist devices, transplantation, and reduction ventriculoplasty.