Table of Contents Author Guidelines Submit a Manuscript
International Journal of Hypertension
Volume 2016, Article ID 5830192, 11 pages
Research Article

Changes in Angiotensin Receptor Distribution and in Aortic Morphology Are Associated with Blood Pressure Control in Aged Metabolic Syndrome Rats

1Department of Physiology, Instituto Nacional de Cardiología “Ignacio Chávez”, 14080 Mexico City, DF, Mexico
2Department of Pathology, Instituto Nacional de Cardiología “Ignacio Chávez”, 14080 Mexico City, DF, Mexico
3National Laboratory of Nanoscience and Nanotechnology, Molecular Biology Division, Instituto Potosino de Investigación Científica y Tecnológica (IPICYT), 78216 San Luis Potosí, SLP, Mexico
4Laboratorio de Nutrición Experimental, Instituto Nacional de Pediatría, 04530 Mexico City, DF, Mexico

Received 4 January 2016; Revised 22 April 2016; Accepted 27 April 2016

Academic Editor: Tomohiro Katsuya

Copyright © 2016 Verónica Guarner-Lans et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


The role of the renin-angiotensin system (RAS) in blood pressure regulation in MS during aging is unknown. It participates in metabolic syndrome (MS) and aging regulating vascular tone and remodeling. RAS might participate in a compensatory mechanism decreasing blood pressure and allowing MS rats to reach 18 months of age and it might form part of therapeutical procedures to ameliorate MS. We studied histological changes and distribution of RAS receptors in aortas of MS aged rats. Electron microscopy images showed premature aging in MS since the increased fibrosis, enlarged endothelium, and invasion of this layer by muscle cells that was present in control 18-month-old aortas were also found in 6-month-old aortas from MS rats. AT1, AT2, and Mas receptors mediate the effects of Ang II and Ang 1-7, respectively. Fluorescence from AT2 decreased with age in control and MS aortas, while fluorescence of AT1 increased in aortas from MS rats at 6 months and diminished during aging. Mas expression increased in MS rats and remained unchanged in control rats. In conclusion, there is premature aging in the aortas from MS rats and the elevated expression of Mas receptor might contribute to decrease blood pressure during aging in MS.