Donate Help Contact The AHA Sign In Home
American Heart Association
Hypertension
Search: search_blue_button Advanced Search
Hypertension. 1995;25:437-442

This Article
Right arrow Full Text
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Inserra, F.
Right arrow Articles by Ferder, L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Inserra, F.
Right arrow Articles by Ferder, L.

(Hypertension. 1995;25:437-442.)
© 1995 American Heart Association, Inc.


Articles

Cardiovascular Changes by Long-term Inhibition of the Renin-Angiotensin System in Aging

Felipe Inserra; Luis Romano; Liliana Ercole; Elena M.V. de Cavanagh; León Ferder

From the Institute of Nephrology, Jewish Hospital, Buenos Aires, Argentina.

Abstract We studied four groups of 20 female mice to evaluate the long-term effect of an angiotensin-converting enzyme on myocardium and vessels during the natural process of aging. Three groups received enalapril in water from weaning to 24 months of age (group A, 20 mg/L; group B, 10 mg/L; group C, 5 mg/L); group D served as a control. Animals surviving after 24 months were killed, and morphometric studies were performed. Total corporal weight was higher in animals receiving enalapril. Cardiac weight relative to total body weight was lower in the treated groups than in the control group. Cardiac morphometric studies showed lower myocardiosclerosis in animals receiving angiotensin-converting enzyme inhibitor (groups A through D, respectively, 0.9±0.6%, 1.1±0.2%, 1.03±0.1%, and 9.5±4.3%; P<.01, groups A, B, and C versus D). The number of mitochondria per myocardiocyte was higher in the groups receiving enalapril (A through D, respectively, 85±7, 85±6, 83±8, and 58±8; P<.01, groups A, B, and C versus D). At the vascular level, vessel diameters were not significantly different between the groups receiving angiotensin-converting enzyme inhibitor and the control group, whereas differences were seen in arterial tunica media thickness (wall-lumen ratio) (groups A through D, respectively, aorta: 0.13±0.02, 0.11±0.02, 0.12±0.01, 2.81±0.35; intrapulmonary: 0.9±0.43, 0.6±0.41, 0.8±0.46, 1.9±0.51; intracerebral: 2.18±0.46, 2.29±0.45, 2.46±0.43, 3.30±0.41; intrarenal: 2.28±0.46, 2.73±0.48, 2.70±0.51, 3.23±0.41; intracariaciac: 2.27±0.44, 2.59±0.41, 2.80±0.43, 3.68±0.47; P<.001, groups A, B, and C versus D). No significant differences in blood pressure were found among the groups. We conclude that cardiovascular changes in aging may be altered by angiotensin-converting enzyme inhibitors.


Key Words: aging • heart • sclerosis • blood vessels • angiotensin-converting enzyme inhibitors • renin- angiotensin system




This article has been cited by other articles:


Home page
CirculationHome page
D.-F. Dai, L. F. Santana, M. Vermulst, D. M. Tomazela, M. J. Emond, M. J. MacCoss, K. Gollahon, G. M. Martin, L. A. Loeb, W. C. Ladiges, et al.
Overexpression of Catalase Targeted to Mitochondria Attenuates Murine Cardiac Aging
Circulation, June 2, 2009; 119(21): 2789 - 2797.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Heart Circ. Physiol.Home page
E. M. de Cavanagh, M. Ferder, F. Inserra, and L. Ferder
Angiotensin II, mitochondria, cytoskeletal, and extracellular matrix connections: an integrating viewpoint
Am J Physiol Heart Circ Physiol, March 1, 2009; 296(3): H550 - H558.
[Abstract] [Full Text] [PDF]


Home page
Cardiovasc ResHome page
L.-J. Min, M. Mogi, J. Iwanami, J.-M. Li, A. Sakata, T. Fujita, K. Tsukuda, M. Iwai, and M. Horiuchi
Cross-talk between aldosterone and angiotensin II in vascular smooth muscle cell senescence
Cardiovasc Res, December 1, 2007; 76(3): 506 - 516.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
E. M. V. de Cavanagh, J. E. Toblli, L. Ferder, B. Piotrkowski, I. Stella, and F. Inserra
Renal mitochondrial dysfunction in spontaneously hypertensive rats is attenuated by losartan but not by amlodipine
Am J Physiol Regulatory Integrative Comp Physiol, June 1, 2006; 290(6): R1616 - R1625.
[Abstract] [Full Text] [PDF]


Home page
Journals of Gerontology Series A: Biological Sciences and Medical SciencesHome page
C. S. Carter, G. Onder, S. B. Kritchevsky, and M. Pahor
Angiotensin-Converting Enzyme Inhibition Intervention in Elderly Persons: Effects on Body Composition and Physical Performance
J. Gerontol. A Biol. Sci. Med. Sci., November 1, 2005; 60(11): 1437 - 1446.
[Abstract] [Full Text] [PDF]


Home page
J. Thorac. Cardiovasc. Surg.Home page
P. Sergeant, E. Blackstone, and B. Meyns
Is return of angina after coronary artery bypass grafting immutable, can it be delayed, and is it important?
J. Thorac. Cardiovasc. Surg., September 1, 1998; 116(3): 440 - 444.
[Abstract] [Full Text]