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Targeting Renin–Angiotensin System Against Alzheimer’s Disease
Renin Angiotensin System (RAS) is a hormonal system that regulates blood pressure and fluid balance through a coordinated action of renal, cardiovascular, and central nervous systems. In addition to its hemodynamic regulatory role, RAS involves in many brain activities, including memory acquisition...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5937164/ https://www.ncbi.nlm.nih.gov/pubmed/29760662 http://dx.doi.org/10.3389/fphar.2018.00440 |
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author | Gebre, Abadi Kahsu Altaye, Birhanetensay Masresha Atey, Tesfay Mehari Tuem, Kald Beshir Berhe, Derbew Fikadu |
author_facet | Gebre, Abadi Kahsu Altaye, Birhanetensay Masresha Atey, Tesfay Mehari Tuem, Kald Beshir Berhe, Derbew Fikadu |
author_sort | Gebre, Abadi Kahsu |
collection | PubMed |
description | Renin Angiotensin System (RAS) is a hormonal system that regulates blood pressure and fluid balance through a coordinated action of renal, cardiovascular, and central nervous systems. In addition to its hemodynamic regulatory role, RAS involves in many brain activities, including memory acquisition and consolidation. This review has summarized the involvement of RAS in the pathology of Alzheimer’s disease (AD), and the outcomes of treatment with RAS inhibitors. We have discussed the effect of brain RAS in the amyloid plaque (Aβ) deposition, oxidative stress, neuroinflammation, and vascular pathology which are directly and indirectly associated with AD. Angiotensin II (AngII) via AT1 receptor is reported to increase brain Aβ level via different mechanisms including increasing amyloid precursor protein (APP) mRNA, β-secretase activity, and presenilin expression. Similarly, it was associated with tau phosphorylation, and reactive oxygen species generation. However, these effects are counterbalanced by Ang II mediated AT2 signaling. The protective effect observed with angiotensin receptor blockers (ARBs) and angiotensin converting enzyme inhibitors (ACEIs) could be as the result of inhibition of Ang II signaling. ARBs also offer additional benefit by shifting the effect of Ang II toward AT2 receptor. To conclude, targeting RAS in the brain may benefit patients with AD though it still requires further in depth understanding. |
format | Online Article Text |
id | pubmed-5937164 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-59371642018-05-14 Targeting Renin–Angiotensin System Against Alzheimer’s Disease Gebre, Abadi Kahsu Altaye, Birhanetensay Masresha Atey, Tesfay Mehari Tuem, Kald Beshir Berhe, Derbew Fikadu Front Pharmacol Pharmacology Renin Angiotensin System (RAS) is a hormonal system that regulates blood pressure and fluid balance through a coordinated action of renal, cardiovascular, and central nervous systems. In addition to its hemodynamic regulatory role, RAS involves in many brain activities, including memory acquisition and consolidation. This review has summarized the involvement of RAS in the pathology of Alzheimer’s disease (AD), and the outcomes of treatment with RAS inhibitors. We have discussed the effect of brain RAS in the amyloid plaque (Aβ) deposition, oxidative stress, neuroinflammation, and vascular pathology which are directly and indirectly associated with AD. Angiotensin II (AngII) via AT1 receptor is reported to increase brain Aβ level via different mechanisms including increasing amyloid precursor protein (APP) mRNA, β-secretase activity, and presenilin expression. Similarly, it was associated with tau phosphorylation, and reactive oxygen species generation. However, these effects are counterbalanced by Ang II mediated AT2 signaling. The protective effect observed with angiotensin receptor blockers (ARBs) and angiotensin converting enzyme inhibitors (ACEIs) could be as the result of inhibition of Ang II signaling. ARBs also offer additional benefit by shifting the effect of Ang II toward AT2 receptor. To conclude, targeting RAS in the brain may benefit patients with AD though it still requires further in depth understanding. Frontiers Media S.A. 2018-04-30 /pmc/articles/PMC5937164/ /pubmed/29760662 http://dx.doi.org/10.3389/fphar.2018.00440 Text en Copyright © 2018 Gebre, Altaye, Atey, Tuem and Berhe. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology Gebre, Abadi Kahsu Altaye, Birhanetensay Masresha Atey, Tesfay Mehari Tuem, Kald Beshir Berhe, Derbew Fikadu Targeting Renin–Angiotensin System Against Alzheimer’s Disease |
title | Targeting Renin–Angiotensin System Against Alzheimer’s Disease |
title_full | Targeting Renin–Angiotensin System Against Alzheimer’s Disease |
title_fullStr | Targeting Renin–Angiotensin System Against Alzheimer’s Disease |
title_full_unstemmed | Targeting Renin–Angiotensin System Against Alzheimer’s Disease |
title_short | Targeting Renin–Angiotensin System Against Alzheimer’s Disease |
title_sort | targeting renin–angiotensin system against alzheimer’s disease |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5937164/ https://www.ncbi.nlm.nih.gov/pubmed/29760662 http://dx.doi.org/10.3389/fphar.2018.00440 |
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