International Journal of Hypertension

Angiotensin-(1-7)/Angiotensin-Converting Enzyme 2/Mas Receptor Axis and Related Mechanisms


Publishing date
01 Feb 2012
Status
Published
Submission deadline
01 Aug 2011

1Department of Morphology, Federal University of Minas Gerais, 31.270-901 Belo Horizonte, MG, Brazil

2Department of Physiology and Functional Genomics, College of Medicine, University of Florida, P.O. Box, Gainesville, FL 100274, USA


Angiotensin-(1-7)/Angiotensin-Converting Enzyme 2/Mas Receptor Axis and Related Mechanisms

Description

Cardiovascular disease is America's leading health problem, and the leading cause of death. One person in three suffers from some form of cardiovascular disease. There is an urgent need to develop new therapeutic strategies to improve the cardiovascular diseases outcome. Very recent studies have demonstrated that the heptapeptide Angiotensin(Ang)-(1-7) holds important cardiovascular beneficial effects. These actions are generally mediated by activation of the G protein-coupled receptor Mas. As a result of these novel findings, Ang-(1-7), in combination with Mas and Angiotensin-converting enzyme (ACE) 2, the main enzyme involved in its formation, is thought to compose a cardioprotective branch within the renin-angiotensin system (RAS), which balances the ACE/Ang II/AT1 receptor effects. Consequently, new therapeutic approaches targeting the ACE2/Ang-(1-7)/Mas axis have been proposed.

We invite investigators to contribute original research articles as well as review articles that will stimulate the continuing efforts to understand the role of this axis on the cardiovascular system. We are particularly interested in articles describing advances in therapeutic approaches based on the ACE2/Ang-(1-7)/Mas axis to treat cardiovascular diseases. Potential topics include, but are not limited to:

  • Signaling pathways triggered by Mas activation
  • New insights into the ACE2/Ang-(1-7)/Mas axis using animal models
  • Innovative pharmacological therapies for cardiovascular diseases and pulmonary diseases based on the ACE2/Ang-(1-7)/Mas axis
  • Gene therapy strategies using ACE2, Ang-(1-7) and Mas
  • Inflammation, cardiovascular diseases, and ACE2/Ang-(1-7)/Mas axis
  • Brain, neurogenic hypertension, stroke, and ACE2/Ang-(1-7)/Mas axis

Articles published in this special issue will not be subject to the journal's Article Processing Charges.

Before submission authors should carefully read over the journal's Author Guidelines, which are located at http://www.hindawi.com/journals/ijht/guidelines/. Prospective authors should submit an electronic copy of their complete manuscript through the journal Manuscript Tracking System at http://mts.hindawi.com/ according to the following timetable:


Articles

  • Special Issue
  • - Volume 2012
  • - Article ID 724240
  • - Research Article

From Rat to Human: Regulation of Renin-Angiotensin System Genes by Sry

Jeremy W. Prokop | Ingrid Kazue Mizuno Watanabe | ... | Amy Milsted
  • Special Issue
  • - Volume 2012
  • - Article ID 594361
  • - Review Article

Protective Role of the ACE2/Ang-(1–9) Axis in Cardiovascular Remodeling

María Paz Ocaranza | Jorge E. Jalil
  • Special Issue
  • - Volume 2012
  • - Article ID 192567
  • - Research Article

Differential Mechanisms of Ang (1-7)-Mediated Vasodepressor Effect in Adult and Aged Candesartan-Treated Rats

S. Bosnyak | R. E. Widdop | ... | E. S. Jones
  • Special Issue
  • - Volume 2012
  • - Article ID 121740
  • - Review Article

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

Marcio Augusto Fressatto de Godoy | Larissa Pernomian | ... | Satish Rattan
  • Special Issue
  • - Volume 2012
  • - Article ID 307315
  • - Review Article

Angiotensin-Converting Enzyme 2: The First Decade

Nicola E. Clarke | Anthony J. Turner
  • Special Issue
  • - Volume 2012
  • - Article ID 536426
  • - Research Article

The Effect of the Thioether-Bridged, Stabilized Angiotensin-(1–7) Analogue Cyclic Ang-(1–7) on Cardiac Remodeling and Endothelial Function in Rats with Myocardial Infarction

Matej Durik | Richard van Veghel | ... | Anton J. M. Roks
International Journal of Hypertension
 Journal metrics
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Acceptance rate8%
Submission to final decision110 days
Acceptance to publication13 days
CiteScore3.600
Journal Citation Indicator0.410
Impact Factor1.9
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