A role for the brain RAS in Alzheimer's and Parkinson's diseases

The brain renin-angiotensin system (RAS) has available the necessary functional components to produce the active ligands angiotensins II, III, IV, angiotensin (1-7), and angiotensin (3-7). These ligands interact with several receptor proteins including AT1, AT2, AT4 and Mas distributed within the c...

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Main Authors: John William Wright, Leen H Kawas, Joseph W Harding
Format: Article
Language:English
Published: Frontiers Media S.A. 2013-10-01
Series:Frontiers in Endocrinology
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fendo.2013.00158/full
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spelling doaj-63f8cb56e62e415ea90db0c0e68e5e832020-11-25T01:03:09ZengFrontiers Media S.A.Frontiers in Endocrinology1664-23922013-10-01410.3389/fendo.2013.0015865435A role for the brain RAS in Alzheimer's and Parkinson's diseasesJohn William Wright0Leen H Kawas1Joseph W Harding2Washington State UniversityWashington State UniversityWashington State UniversityThe brain renin-angiotensin system (RAS) has available the necessary functional components to produce the active ligands angiotensins II, III, IV, angiotensin (1-7), and angiotensin (3-7). These ligands interact with several receptor proteins including AT1, AT2, AT4 and Mas distributed within the central and peripheral nervous systems as well as local RASs in several organs. This review first describes the enzymatic pathways in place to synthesize these ligands and the binding characteristics of these angiotensin receptor subtypes. We next discuss current hypotheses to explain the disorders of Alzheimer’s disease (AD) and Parkinson’s disease (PD), as well as research efforts focused on the use of angiotensin converting enzyme (ACE) inhibitors and angiotensin receptor blockers (ARBs), in their treatment. ACE inhibitors and ARBs are showing promise in the treatment of several neurodegenerative pathologies; however, there is a need for the development of analogues capable of penetrating the blood-brain barrier and acting as agonists or antagonists at these receptor sites. Angiotensins II (AngII) and IV (Ang(IV) have been shown to play opposing roles regarding memory acquisition and consolidation in animal models. We discuss the development of efficacious AngIV analogues in the treatment of animal models of AD and PD. These AngIV analogues act via the AT4 receptor subtype which may coincide with the hepatocyte growth factor (HGF)/c-Met receptor system. Finally, future research directions are described concerning new approaches to the treatment of these two neurological diseases.http://journal.frontiersin.org/Journal/10.3389/fendo.2013.00158/fullAngiotensin IIHepatocyte Growth FactorAngiotensin IVangiotensin receptorsc-Met receptorMas receptor
collection DOAJ
language English
format Article
sources DOAJ
author John William Wright
Leen H Kawas
Joseph W Harding
spellingShingle John William Wright
Leen H Kawas
Joseph W Harding
A role for the brain RAS in Alzheimer's and Parkinson's diseases
Frontiers in Endocrinology
Angiotensin II
Hepatocyte Growth Factor
Angiotensin IV
angiotensin receptors
c-Met receptor
Mas receptor
author_facet John William Wright
Leen H Kawas
Joseph W Harding
author_sort John William Wright
title A role for the brain RAS in Alzheimer's and Parkinson's diseases
title_short A role for the brain RAS in Alzheimer's and Parkinson's diseases
title_full A role for the brain RAS in Alzheimer's and Parkinson's diseases
title_fullStr A role for the brain RAS in Alzheimer's and Parkinson's diseases
title_full_unstemmed A role for the brain RAS in Alzheimer's and Parkinson's diseases
title_sort role for the brain ras in alzheimer's and parkinson's diseases
publisher Frontiers Media S.A.
series Frontiers in Endocrinology
issn 1664-2392
publishDate 2013-10-01
description The brain renin-angiotensin system (RAS) has available the necessary functional components to produce the active ligands angiotensins II, III, IV, angiotensin (1-7), and angiotensin (3-7). These ligands interact with several receptor proteins including AT1, AT2, AT4 and Mas distributed within the central and peripheral nervous systems as well as local RASs in several organs. This review first describes the enzymatic pathways in place to synthesize these ligands and the binding characteristics of these angiotensin receptor subtypes. We next discuss current hypotheses to explain the disorders of Alzheimer’s disease (AD) and Parkinson’s disease (PD), as well as research efforts focused on the use of angiotensin converting enzyme (ACE) inhibitors and angiotensin receptor blockers (ARBs), in their treatment. ACE inhibitors and ARBs are showing promise in the treatment of several neurodegenerative pathologies; however, there is a need for the development of analogues capable of penetrating the blood-brain barrier and acting as agonists or antagonists at these receptor sites. Angiotensins II (AngII) and IV (Ang(IV) have been shown to play opposing roles regarding memory acquisition and consolidation in animal models. We discuss the development of efficacious AngIV analogues in the treatment of animal models of AD and PD. These AngIV analogues act via the AT4 receptor subtype which may coincide with the hepatocyte growth factor (HGF)/c-Met receptor system. Finally, future research directions are described concerning new approaches to the treatment of these two neurological diseases.
topic Angiotensin II
Hepatocyte Growth Factor
Angiotensin IV
angiotensin receptors
c-Met receptor
Mas receptor
url http://journal.frontiersin.org/Journal/10.3389/fendo.2013.00158/full
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