Alamandine: a new member of the angiotensin family

Curr Opin Nephrol Hypertens. 2014 Mar;23(2):130-4. doi: 10.1097/01.mnh.0000441052.44406.92.

Abstract

Purpose of review: In this article, we review the recent findings regarding a new derivative of angiotensin-(1-7) [Ang-(1-7)], alamandine, and its receptor, the Mas-related G-coupled receptor type D (MrgD) with a special emphasis on its role and how it can be formed.

Recent findings: Over the last decade, there have been significant conceptual changes regarding the understanding of the renin-angiotensin system (RAS). A cardioprotective axis has been elucidated by the discovery of the Mas receptor for the biologically active Ang-(1-7), and the angiotensin-converting enzyme 2 (ACE2) that coverts Ang II into Ang-(1-7). In addition, several components of the system, such as Ang-(1-12), Angiotensin A (Ang A) and the newly discovered peptide, alamandine, have been identified. Alamandine is generated by catalysis of Ang A via ACE2 or directly from Ang-(1-7).

Summary: Alamandine is a vasoactive peptide with similar protective actions as Ang-(1-7) that acts through the MrgD and may represent another important counter-regulatory mechanism within the RAS.

Publication types

  • Review

MeSH terms

  • Angiotensin I / metabolism
  • Angiotensin-Converting Enzyme 2
  • Angiotensins / metabolism
  • Animals
  • Humans
  • Oligopeptides / metabolism*
  • Peptide Fragments / metabolism
  • Peptidyl-Dipeptidase A / metabolism
  • Receptors, G-Protein-Coupled / metabolism
  • Renin-Angiotensin System*
  • Signal Transduction

Substances

  • Angiotensins
  • Oligopeptides
  • Peptide Fragments
  • Receptors, G-Protein-Coupled
  • alamandine
  • angiotensin A
  • Angiotensin I
  • Peptidyl-Dipeptidase A
  • ACE2 protein, human
  • Angiotensin-Converting Enzyme 2
  • angiotensin I (1-7)