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Hypertension. 2002;39:75-80
doi: 10.1161/hy0102.100788
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(Hypertension. 2002;39:75.)
© 2002 American Heart Association, Inc.


Scientific Contributions

Stimulation of Cardiac Apoptosis in Essential Hypertension

Potential Role of Angiotensin II

Arantxa González; Begoña López; Susana Ravassa; Ramón Querejeta; Mariano Larman; Javier Díez; María A. Fortuño

From the Division of Cardiovascular Pathophysiology, School of Medicine, University of Navarra (A.G., B.L., S.R., J.D., M.A.F.), Pamplona; Division of Cardiology, Ntra Sra de Aránzazu Hospital (R.Q.), San Sebastian; Division of Hemodynamics, Guipuzcoa Polyclinic (M.L.), San Sebastián; and the Department of Cardiology and Cardiovascular Surgery, University Clinic, University of Navarra (J.D.), Pamplona, Spain.

Correspondence to Maria Antonia Fortuño, División de Fisiopatología Cardiovascular, Facultad de Medicina, Universidad de Navarra, C/Irunlarrea s/n, 31080 Pamplona, Spain. E-mail fortuto{at}unav.es

We investigated whether cardiac apoptosis is stimulated in the heart of hypertensive patients and whether angiotensin II plays a role in such alteration. The study was performed in 28 patients with essential hypertension and no evidence of either ischemic cardiomyopathy or heart failure. After randomization, 14 patients were assigned to losartan and 14 patients to amlodipine treatment. At baseline and after 12 months, right septal endomyocardial biopsies were performed, and the number of apoptotic nuclei was assessed by DNA end-labeling (TUNEL). In addition, immunostaining for the active form of caspase-3 was also performed to assess apoptosis. Compared with normotensive autopsied hearts, both cardiomyocyte and noncardiomyocyte apoptosis were increased (P<0.001) in hypertensive hearts. Time-course changes in blood pressure during treatment were similar in the 2 groups of patients. In losartan-treated patients, both cardiomyocyte and noncardiomyocyte apoptosis decreased (P<0.05). Neither cardiomyocyte nor noncardiomyocyte apoptosis changed significantly in amlodipine-treated patients. These findings indicate that apoptosis is abnormally stimulated in the heart of patients with essential hypertension. Our data also suggest that the ability of antihypertensive treatment to inhibit cardiac apoptosis is independent of its antihypertensive efficacy. We propose that angiotensin II may participate in the stimulation of cardiac apoptosis in essential hypertension.


Key Words: amlodipine • angiotensin II • apoptosis • heart • hypertension, essential • losartan




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