Angiotensin-(1-7) and angiotensin-(1-9): function in cardiac and vascular remodelling

Clare A McKinney1, Caroline Fattah1, Christopher M Loughrey1

  • 1*Institute of Cardiovascular and Medical Sciences, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, U.K.

Insights

The renin-angiotensin system (RAS) regulates cardiovascular function. Counter-regulatory peptides, angiotensin-(1-7) and angiotensin-(1-9), protect against cardiovascular disease by opposing harmful RAS effects.

Area of Science:

  • Cardiovascular Physiology
  • Endocrinology
  • Molecular Biology

Background:

  • The renin-angiotensin system (RAS) is crucial for cardiovascular homeostasis.
  • Dysregulation of the RAS, particularly angiotensin II (AngII) acting via the AT1 receptor, drives cardiovascular disease (CVD) pathophysiology, including heart failure and atherosclerosis.
  • The ACE2-angiotensin-(1-7)-Mas receptor axis acts as a counter-regulatory pathway, mitigating AngII's detrimental effects.

Purpose of the Study:

  • To review the cardiovascular roles of the counter-regulatory RAS peptides angiotensin-(1-7) and angiotensin-(1-9).
  • To focus on the effects of these peptides in cardiac and vascular remodeling.
  • To highlight their protective functions in the context of cardiovascular disease.

Main Methods:

  • Literature review of existing studies on RAS peptides.
  • Analysis of research on angiotensin-(1-7) and angiotensin-(1-9) signaling pathways.
  • Synthesis of findings related to cardiovascular remodeling.

Main Results:

  • Angiotensin-(1-7), produced by ACE2 from AngII, antagonizes AngII's pro-remodeling effects via the Mas receptor.
  • Angiotensin-(1-9), another ACE2 metabolite, is also recognized as a biologically active peptide within the counter-regulatory RAS axis.
  • Both peptides play significant roles in modulating cardiac and vascular remodeling processes.

Conclusions:

  • The counter-regulatory RAS axis, involving angiotensin-(1-7) and angiotensin-(1-9), offers a protective counterbalance to the pro-pathogenic effects of AngII.
  • Targeting these peptides may represent a therapeutic strategy for cardiovascular diseases.
  • Further research into the precise mechanisms of angiotensin-(1-9) is warranted.

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