Organisation and functional role of the brain angiotensin system

The discovery that all components of the renin-angiotensin system (RAS) are present in the brain led investigators to postulate the existence of a local brain RAS. Supporting this, angiotensin immunoreactive neurones have been visualised in the brain. Two major pathways were described: a forebrain p...

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Main Authors: Catherine Llorens-Cortes, Frederic Ao Mendelsohn
Format: Article
Language:English
Published: Hindawi - SAGE Publishing 2002-03-01
Series:Journal of the Renin-Angiotensin-Aldosterone System
Online Access:http://jra.sagepub.com/content/3/1_suppl/39.full.pdf
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spelling doaj-1ead0d5e46ab46d48c4cd7588c5d0d0a2021-05-02T20:27:55ZengHindawi - SAGE PublishingJournal of the Renin-Angiotensin-Aldosterone System1470-32031752-89762002-03-0131_suppl394810.3317/JRAAS.2002.02910.3317_JRAAS.2002.029Organisation and functional role of the brain angiotensin systemCatherine Llorens-CortesFrederic Ao MendelsohnThe discovery that all components of the renin-angiotensin system (RAS) are present in the brain led investigators to postulate the existence of a local brain RAS. Supporting this, angiotensin immunoreactive neurones have been visualised in the brain. Two major pathways were described: a forebrain pathway which connects circumventricular organs to the median preoptic nucleus, paraventricular and supraoptic nuclei, and a second pathway connecting the hypothalamus to the medulla oblongata. Blood-brain-barrier deficient circumventricular organs are rich in angiotensin II (Ang II) receptors. By activating these receptors, circulating Ang II may act on central cardiovascular centres via angiotensinergic neurones, providing a link between peripheral and central Ang II systems. Among the effector peptides of the brain RAS, Ang II and angiotensin III (Ang III) have the same affinity for type 1 and type 2 Ang II receptors. When injected into the brain, both peptides increase blood pressure (BP), water intake and pituitary hormone release and may modify learning and memory. Since Ang II is converted in vivo to Ang III, the nature of the true effector is unknown. This review summarises new insights into the predominant role of brain Ang III in the control of BP and underlines the fact that brain aminopeptidase A, the enzyme forming central Ang III, could constitute a putative central therapeutic target for the treatment of hypertension.http://jra.sagepub.com/content/3/1_suppl/39.full.pdf
collection DOAJ
language English
format Article
sources DOAJ
author Catherine Llorens-Cortes
Frederic Ao Mendelsohn
spellingShingle Catherine Llorens-Cortes
Frederic Ao Mendelsohn
Organisation and functional role of the brain angiotensin system
Journal of the Renin-Angiotensin-Aldosterone System
author_facet Catherine Llorens-Cortes
Frederic Ao Mendelsohn
author_sort Catherine Llorens-Cortes
title Organisation and functional role of the brain angiotensin system
title_short Organisation and functional role of the brain angiotensin system
title_full Organisation and functional role of the brain angiotensin system
title_fullStr Organisation and functional role of the brain angiotensin system
title_full_unstemmed Organisation and functional role of the brain angiotensin system
title_sort organisation and functional role of the brain angiotensin system
publisher Hindawi - SAGE Publishing
series Journal of the Renin-Angiotensin-Aldosterone System
issn 1470-3203
1752-8976
publishDate 2002-03-01
description The discovery that all components of the renin-angiotensin system (RAS) are present in the brain led investigators to postulate the existence of a local brain RAS. Supporting this, angiotensin immunoreactive neurones have been visualised in the brain. Two major pathways were described: a forebrain pathway which connects circumventricular organs to the median preoptic nucleus, paraventricular and supraoptic nuclei, and a second pathway connecting the hypothalamus to the medulla oblongata. Blood-brain-barrier deficient circumventricular organs are rich in angiotensin II (Ang II) receptors. By activating these receptors, circulating Ang II may act on central cardiovascular centres via angiotensinergic neurones, providing a link between peripheral and central Ang II systems. Among the effector peptides of the brain RAS, Ang II and angiotensin III (Ang III) have the same affinity for type 1 and type 2 Ang II receptors. When injected into the brain, both peptides increase blood pressure (BP), water intake and pituitary hormone release and may modify learning and memory. Since Ang II is converted in vivo to Ang III, the nature of the true effector is unknown. This review summarises new insights into the predominant role of brain Ang III in the control of BP and underlines the fact that brain aminopeptidase A, the enzyme forming central Ang III, could constitute a putative central therapeutic target for the treatment of hypertension.
url http://jra.sagepub.com/content/3/1_suppl/39.full.pdf
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