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European Journal of Heart Failure 2002 4(5):583-586; doi:10.1016/S1388-9842(02)00091-0
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© 2002 European Society of Cardiology

Simultaneous angiotensin converting enzyme inhibition moderates ventricular dysfunction caused by doxorubicin

Mikhail Vaynblata,*, Himansu R. Shahb, Dinesh Bhaskarana, Geeta Ramdevb, Wellington J. Davis, IIIa, Joseph N. Cunningham, Jr.a,b and Mario Chiavarellib

a Division of Cardiovascular Surgery, Department of Surgery, Maimomides Medical Center, Administration Building, Rm D, Department of Surgery 4802 10th Ave, Brooklyn, NY 11219, USA
b Division of Cardiothoracic Surgery, Department of Surgery, State University of New York-Health Science Center (SUNY-HSC) at Brooklyn Brooklyn, NY, USA

* Corresponding author: Tel.: +1-718-283-7686; fax: +1-718-283-7392. E-mail address: mishavayn{at}aol.com


   Abstract

Aims: The purpose of this study was to determine that the administration of an angiotensin converting enzyme (ACE) inhibitor enalapril would confer protection against doxorubicin-induced experimental heart failure, and attenuate the development of left ventricular dysfunction.

Methods: Seventeen dogs were chronically instrumented with an intracoronary catheter and received doxorubicin weekly for 4 weeks. Animals were assigned to two groups: group 1: untreated heart failure; and group 2: simultaneous enalapril administration (5 mg twice a week). Hemodynamic data were obtained at week 0 and 12. Echocardiography was performed weekly.

Results: Survival improved with simultaneous enalapril administration (36% in group 1 vs. 100% in group 2, P=0.04). The increase in the left ventricular end-diastolic pressure was significantly reduced at week 12 (17±1 mmHg in group 1 vs. 9±1 mmHg in group 2, P=0.0042). The fall in left ventricular stroke work index was significantly prevented (52% in group 1 vs. 21% in group 2, P=0.006). The increase in right ventricular end-diastolic diameter was significantly reduced by enalapril prophylaxis.

Conclusion: Simultaneous treatment with enalapril was beneficial in the prevention of doxorubicin-induced cardiomyopathy.

Key Words: Heart failure • Cardiomyopathy • Dog • ACE inhibitors • Ventricular function

Received March 29, 2001; Revised February 7, 2002; Accepted April 25, 2002


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