Effect of captopril on myocardial β-adrenoceptor density and G-proteins in patients with mild to moderate heart failure due to dilated cardiomyopathy

H. Jakob, T. Eschenhagen, U. Mende, M. Patten, W. Schmitz, H. Scholz, J. Schulte am Esch, M. Steinfath, M. Sigmund and P. Hanrath, et al.

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Abstract

In end-stage heart failure due to idiopathic dilated cardiomyopathy beta1-adrenoceptors are downregulated and G1agr-proteins are upregulated. The aim of the present study was to investigate the influence of the angiotensin-converting enzyme inhibitor captopril on beta-adrenoceptor density and Giagr-proteins in sequential endomyocardial biopsies. Nineteen patients with mild to moderate congestive heart failure due to idiopathic dilated cardiomyopathy (NYHA Class II–III) were studied before and after 8–11 weeks of therapy. Patients were randomised into a captopril and a control group; 9 patients received captopril 12.5–50 mg per day, (divided in 2–3 doses) p.o. in addition to ldquoconventionalrdquo therapy with digoxin and diuretics, and 10 controls received ldquoconventionalrdquo therapy only. Echocardiography, spiroergometry, right heart catheterisation and endomyocardial biopsies were performed before (baseline) and after treatment. Compared to baseline, captopril increased total beta-adrenoceptor density by selectively increasing beta1-adrenoceptors (31.6 vs 41.2 fmol·mg–1; p<0.05) but="" had="" no="" significant="" effect="" on="">iagr-proteins. The results indicate that treatment with angiotensin-converting enzyme inhibitors partly restores myocardial beta1-adrenoceptor density, and this action effect may contribute to the clinical improvement of patients with idiopathic dilated cardiomyopathy treated in this way.

Key words  Captopril - Dilated cardiomyopathy - ACE-inhibitors - G-proteins - beta-adrenoceptor density

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