Biosynthetic Pathways and the Role of the Mas Receptor in the Effects of Angiotensin-(1–7) in Smooth Muscles

Author:

Fressatto de Godoy Marcio Augusto1,Pernomian Larissa2,de Oliveira Ana Maria3,Rattan Satish1

Affiliation:

1. Division of Gastroenterology & Hepatology, Department of Medicine, Jefferson Medical College, Thomas Jefferson University, Philadelphia, PA, USA

2. Laboratory of Pharmacology, Department of Pharmacology, Faculty of Medicine from Ribeirão Preto, University of São Paulo (USP), Avenida do Café s/n, 14040-903 Ribeirão Preto, SP, Brazil

3. Laboratory of Pharmacology, Department of Physics and Chemistry, Faculty of Pharmaceutical Sciences from Ribeirão Preto, University of São Paulo (USP), Avenida do Café s/n, 14040-903 Ribeirão Preto, SP, Brazil

Abstract

Ang-(1–7) is produced via degradation of Ang II by the human angiotensin converting enzyme, also known as ACE2. In the cardiovascular system, Ang-(1–7) has been shown to produce effects that are opposite to those of Ang II. These include smooth muscle relaxation and cardioprotection. While the roles of Ang-(1–7) in other systems are currently topic of intense research, functional data suggest a relaxation action in gastrointestinal smooth muscles in a way that corroborates the results obtained from vascular tissues. However, more studies are necessary to determine a relevant role for Ang-(1–7) in the gastrointestinal system. The Ang-(1–7) actions are mediated by a distinct, functional, Ang-(1–7) receptor: theMas receptoras shown by diverse studies involving site-specific binding techniques, selective antagonists, and targeted gene deletion. This paper provides an overview of the functional role and the molecular pathways involved in the biosynthesis and activity of Ang-(1–7) in diverse systems.

Funder

National Institutes of Diabetes and Digestive and Kidney Diseases

Publisher

Hindawi Limited

Subject

Internal Medicine

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