Impact of the Renin–Angiotensin System on the Endothelium in Vascular Dementia: Unresolved Issues and Future Perspectives

The effects of the renin–angiotensin system (RAS) surpass the renal and cardiovascular systems to encompass other body tissues and organs, including the brain. Angiotensin II (Ang II), the most potent mediator of RAS in the brain, contributes to vascular dementia via different mechanisms, including...

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Main Authors: Fatima Y. Noureddine, Raffaele Altara, Fan Fan, Andriy Yabluchanskiy, George W. Booz, Fouad A. Zouein
Format: Article
Language:English
Published: MDPI AG 2020-06-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/21/12/4268
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spelling doaj-ceb2704b127041ebae6a2011eae2e4132020-11-25T03:13:13ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672020-06-01214268426810.3390/ijms21124268Impact of the Renin–Angiotensin System on the Endothelium in Vascular Dementia: Unresolved Issues and Future PerspectivesFatima Y. Noureddine0Raffaele Altara1Fan Fan2Andriy Yabluchanskiy3George W. Booz4Fouad A. Zouein5Department of Pharmacology and Toxicology, Faculty of Medicine, American University of Beirut, Beirut 1107 2020, LebanonInstitute for Experimental Medical Research, Oslo University Hospital and University of Oslo, and KG Jebsen Center for Cardiac Research, 0424 Oslo, NorwayDepartment of Pharmacology and Toxicology, School of Medicine, The University of Mississippi Medical Center, Jackson, MS 39216, USACenter for Geroscience and Healthy Brain Aging, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USADepartment of Pharmacology and Toxicology, School of Medicine, The University of Mississippi Medical Center, Jackson, MS 39216, USADepartment of Pharmacology and Toxicology, Faculty of Medicine, American University of Beirut, Beirut 1107 2020, LebanonThe effects of the renin–angiotensin system (RAS) surpass the renal and cardiovascular systems to encompass other body tissues and organs, including the brain. Angiotensin II (Ang II), the most potent mediator of RAS in the brain, contributes to vascular dementia via different mechanisms, including neuronal homeostasis disruption, vascular remodeling, and endothelial dysfunction caused by increased inflammation and oxidative stress. Other RAS components of emerging significance at the level of the blood–brain barrier include angiotensin-converting enzyme 2 (ACE2), Ang(1–7), and the AT2, Mas, and AT4 receptors. The various angiotensin hormones perform complex actions on brain endothelial cells and pericytes through specific receptors that have either detrimental or beneficial actions. Increasing evidence indicates that the ACE2/Ang(1–7)/Mas axis constitutes a protective arm of RAS on the blood–brain barrier. This review provides an update of studies assessing the different effects of angiotensins on cerebral endothelial cells. The involved signaling pathways are presented and help highlight the potential pharmacological targets for the management of cognitive and behavioral dysfunctions associated with vascular dementia.https://www.mdpi.com/1422-0067/21/12/4268blood–brain barrierACE1ACE2AT2 receptorMas receptorAng(1–7)
collection DOAJ
language English
format Article
sources DOAJ
author Fatima Y. Noureddine
Raffaele Altara
Fan Fan
Andriy Yabluchanskiy
George W. Booz
Fouad A. Zouein
spellingShingle Fatima Y. Noureddine
Raffaele Altara
Fan Fan
Andriy Yabluchanskiy
George W. Booz
Fouad A. Zouein
Impact of the Renin–Angiotensin System on the Endothelium in Vascular Dementia: Unresolved Issues and Future Perspectives
International Journal of Molecular Sciences
blood–brain barrier
ACE1
ACE2
AT2 receptor
Mas receptor
Ang(1–7)
author_facet Fatima Y. Noureddine
Raffaele Altara
Fan Fan
Andriy Yabluchanskiy
George W. Booz
Fouad A. Zouein
author_sort Fatima Y. Noureddine
title Impact of the Renin–Angiotensin System on the Endothelium in Vascular Dementia: Unresolved Issues and Future Perspectives
title_short Impact of the Renin–Angiotensin System on the Endothelium in Vascular Dementia: Unresolved Issues and Future Perspectives
title_full Impact of the Renin–Angiotensin System on the Endothelium in Vascular Dementia: Unresolved Issues and Future Perspectives
title_fullStr Impact of the Renin–Angiotensin System on the Endothelium in Vascular Dementia: Unresolved Issues and Future Perspectives
title_full_unstemmed Impact of the Renin–Angiotensin System on the Endothelium in Vascular Dementia: Unresolved Issues and Future Perspectives
title_sort impact of the renin–angiotensin system on the endothelium in vascular dementia: unresolved issues and future perspectives
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1661-6596
1422-0067
publishDate 2020-06-01
description The effects of the renin–angiotensin system (RAS) surpass the renal and cardiovascular systems to encompass other body tissues and organs, including the brain. Angiotensin II (Ang II), the most potent mediator of RAS in the brain, contributes to vascular dementia via different mechanisms, including neuronal homeostasis disruption, vascular remodeling, and endothelial dysfunction caused by increased inflammation and oxidative stress. Other RAS components of emerging significance at the level of the blood–brain barrier include angiotensin-converting enzyme 2 (ACE2), Ang(1–7), and the AT2, Mas, and AT4 receptors. The various angiotensin hormones perform complex actions on brain endothelial cells and pericytes through specific receptors that have either detrimental or beneficial actions. Increasing evidence indicates that the ACE2/Ang(1–7)/Mas axis constitutes a protective arm of RAS on the blood–brain barrier. This review provides an update of studies assessing the different effects of angiotensins on cerebral endothelial cells. The involved signaling pathways are presented and help highlight the potential pharmacological targets for the management of cognitive and behavioral dysfunctions associated with vascular dementia.
topic blood–brain barrier
ACE1
ACE2
AT2 receptor
Mas receptor
Ang(1–7)
url https://www.mdpi.com/1422-0067/21/12/4268
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