Beneficial Effects of Long-Term Administration of an Oral Formulation of Angiotensin-(1–7) in Infarcted Rats

Author:

Marques Fúlvia D.12,Melo Marcos B.1,Souza Leandro E.1,Irigoyen Maria Claúdia C.1,Sinisterra Rúben D.13,de Sousa Frederico B.1,Savergnini Sílvia Q.12,Braga Vinícius B. A.4,Ferreira Anderson J.14,Santos Robson A. S.12

Affiliation:

1. National Institute of Science and Technology in Nanobiopharmaceutics, Federal University of Minas Gerais, 31.270-901 Belo Horizonte, MG, Brazil

2. Department of Physiology and Biophysics, Federal University of Minas Gerais, 31.270-901 Belo Horizonte, MG, Brazil

3. Department of Chemistry, Federal University of Minas Gerais, 31.270-901 Belo Horizonte, MG, Brazil

4. Department of Morphology, Federal University of Minas Gerais, 31.270-901 Belo Horizonte, MG, Brazil

Abstract

In this study was evaluated the chronic cardiac effects of a formulation developed by including angiotensin(Ang)-(1–7) in hydroxypropylβ-cyclodextrin (HPβCD), in infarcted rats. Myocardial infarction (MI) was induced by left coronary artery occlusion. HPβCD/Ang-(1–7) was administered for 60 days (76 μg/Kg/once a day/gavage) starting immediately before infarction. Echocardiography was utilized to evaluate usual cardiac parameters, and radial strain method was used to analyze the velocity and displacement of myocardial fibers at initial time and 15, 30, and 50 days after surgery. Real-time PCR was utilized to evaluate the fibrotic signaling involved in the remodeling process. Once-a-day oral HPβCD/Ang-(1–7) administration improved the cardiac function and reduced the deleterious effects induced by MI on TGF-βand collagen type I expression, as well as on the velocity and displacement of myocardial fibers. These findings confirm cardioprotective effects of Ang-(1–7) and indicate HPβCD/Ang-(1–7) as a feasible formulation for long-term oral administration of this heptapeptide.

Funder

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Publisher

Hindawi Limited

Subject

Internal Medicine

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