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  4. Opportunities for Targeting the Angiotensin-Converting Enzyme 2/Angiotensin-(1-7)/Mas Receptor Pathway in Hypertension
 
research article

Opportunities for Targeting the Angiotensin-Converting Enzyme 2/Angiotensin-(1-7)/Mas Receptor Pathway in Hypertension

Fraga-Silva, Rodrigo Araujo  
•
Ferreira, Anderson Jose
•
Santos, Souza Dos
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2013
Current Hypertension Reports

It is well known that the renin-angiotensin system (RAS) plays a pivotal role in the pathophysiology of cardiovascular diseases. This is well illustrated by the great success of ACE inhibitors and angiotensin (Ang) II AT(1) blockers in the treatment of hypertension and its complications. In the past decade, the classical concept of RAS orchestrated by a series of enzymatic reactions culminating in the linear generation and action of Ang II has expanded and become more complex. From the discoveries of new components such as the angiotensin converting enzyme 2 and the receptor Mas emerged a novel concept of dual opposite branches of the RAS: one vasoconstrictor and pro-hypertensive composed of ACE/Ang II/AT1; and other vasodilator and anti-hypertensive composed of ACE2/Ang-(1-7)/Mas. In this review we will discuss recent findings concerning the biological role of the ACE2/Ang-(1-7)/Mas arm in the cardiovascular system and highlight the initiatives to develop potential therapeutic strategies based on this axis for treating hypertension.

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Type
research article
DOI
10.1007/s11906-012-0324-1
Web of Science ID

WOS:000313518100006

Author(s)
Fraga-Silva, Rodrigo Araujo  
Ferreira, Anderson Jose
Santos, Souza Dos
Augusto, Robson
Date Issued

2013

Publisher

Springer

Published in
Current Hypertension Reports
Volume

15

Issue

1

Start page

31

End page

38

Subjects

Renin-angiotensin system

•

RAS

•

Angiotensin-(1-7)

•

Angiotensin converting enzyme 2

•

Mas receptor

•

Hypertension

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LHTC  
Available on Infoscience
March 28, 2013
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/90846
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