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Updated: May 2, 2026

Receptor Autoradiography Protocol for the Localized Visualization of Angiotensin II Receptors
Published on: June 7, 2016
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.
Abstract:
The RAS (renin-angiotensin system) is integral to cardiovascular physiology; however, dysregulation of this system largely contributes to the pathophysiology of CVD (cardiovascular disease). It is well established that AngII (angiotensin II), the main effector of the RAS, engages the AT1R (angiotensin type 1 receptor) and promotes cell growth, proliferation, migration and oxidative stress, all processes which contribute to remodelling of the heart and vasculature, ultimately leading to the development and progression of various CVDs, including heart failure and atherosclerosis. The counter-regulatory axis of the RAS, which is centred on the actions of ACE2 (angiotensin-converting enzyme 2) and the resultant production of Ang-(1-7) [angiotensin-(1-7)] from AngII, antagonizes the actions of AngII via the receptor Mas, thereby providing a protective role in CVD. More recently, another ACE2 metabolite, Ang-(1-9) [angiotensin-(1-9)], has been reported to be a biologically active peptide within the counter-regulatory axis of the RAS. The present review will discuss the role of the counter-regulatory RAS peptides Ang-(1-7) and Ang-(1-9) in the cardiovascular system, with a focus on their effects in remodelling of the heart and vasculature.
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