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The intracellular renin-angiotensin system: Friend or foe. Some light from the dopaminergic neurons

The renin-angiotensin system (RAS) is one of the oldest hormone systems in vertebrate phylogeny. RAS was initially related to regulation of blood pressure and sodium and water homeostasis. However, local or paracrine RAS were later identified in many tissues, including brain, and play a major role i...

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Autores principales: Labandeira-Garcia, Jose L., Valenzuela, Rita, Costa-Besada, Maria A., Villar-Cheda, Begoña, Rodriguez-Perez, Ana I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7543790/
https://www.ncbi.nlm.nih.gov/pubmed/33039415
http://dx.doi.org/10.1016/j.pneurobio.2020.101919
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author Labandeira-Garcia, Jose L.
Valenzuela, Rita
Costa-Besada, Maria A.
Villar-Cheda, Begoña
Rodriguez-Perez, Ana I.
author_facet Labandeira-Garcia, Jose L.
Valenzuela, Rita
Costa-Besada, Maria A.
Villar-Cheda, Begoña
Rodriguez-Perez, Ana I.
author_sort Labandeira-Garcia, Jose L.
collection PubMed
description The renin-angiotensin system (RAS) is one of the oldest hormone systems in vertebrate phylogeny. RAS was initially related to regulation of blood pressure and sodium and water homeostasis. However, local or paracrine RAS were later identified in many tissues, including brain, and play a major role in their physiology and pathophysiology. In addition, a major component, ACE2, is the entry receptor for SARS-CoV-2. Overactivation of tissue RAS leads several oxidative stress and inflammatory processes involved in aging-related degenerative changes. In addition, a third level of RAS, the intracellular or intracrine RAS (iRAS), with still unclear functions, has been observed. The possible interaction between the intracellular and extracellular RAS, and particularly the possible deleterious or beneficial effects of the iRAS activation are controversial. The dopaminergic system is particularly interesting to investigate the RAS as important functional interactions between dopamine and RAS have been observed in the brain and several peripheral tissues. Our recent observations in mitochondria and nucleus of dopaminergic neurons may clarify the role of the iRAS. This may be important for the developing of new therapeutic strategies, since the effects on both extracellular and intracellular RAS must be taken into account, and perhaps better understanding of COVID-19 cell mechanisms.
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spelling pubmed-75437902020-10-09 The intracellular renin-angiotensin system: Friend or foe. Some light from the dopaminergic neurons Labandeira-Garcia, Jose L. Valenzuela, Rita Costa-Besada, Maria A. Villar-Cheda, Begoña Rodriguez-Perez, Ana I. Prog Neurobiol Review Article The renin-angiotensin system (RAS) is one of the oldest hormone systems in vertebrate phylogeny. RAS was initially related to regulation of blood pressure and sodium and water homeostasis. However, local or paracrine RAS were later identified in many tissues, including brain, and play a major role in their physiology and pathophysiology. In addition, a major component, ACE2, is the entry receptor for SARS-CoV-2. Overactivation of tissue RAS leads several oxidative stress and inflammatory processes involved in aging-related degenerative changes. In addition, a third level of RAS, the intracellular or intracrine RAS (iRAS), with still unclear functions, has been observed. The possible interaction between the intracellular and extracellular RAS, and particularly the possible deleterious or beneficial effects of the iRAS activation are controversial. The dopaminergic system is particularly interesting to investigate the RAS as important functional interactions between dopamine and RAS have been observed in the brain and several peripheral tissues. Our recent observations in mitochondria and nucleus of dopaminergic neurons may clarify the role of the iRAS. This may be important for the developing of new therapeutic strategies, since the effects on both extracellular and intracellular RAS must be taken into account, and perhaps better understanding of COVID-19 cell mechanisms. Elsevier Ltd. 2021-04 2020-10-08 /pmc/articles/PMC7543790/ /pubmed/33039415 http://dx.doi.org/10.1016/j.pneurobio.2020.101919 Text en © 2020 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Review Article
Labandeira-Garcia, Jose L.
Valenzuela, Rita
Costa-Besada, Maria A.
Villar-Cheda, Begoña
Rodriguez-Perez, Ana I.
The intracellular renin-angiotensin system: Friend or foe. Some light from the dopaminergic neurons
title The intracellular renin-angiotensin system: Friend or foe. Some light from the dopaminergic neurons
title_full The intracellular renin-angiotensin system: Friend or foe. Some light from the dopaminergic neurons
title_fullStr The intracellular renin-angiotensin system: Friend or foe. Some light from the dopaminergic neurons
title_full_unstemmed The intracellular renin-angiotensin system: Friend or foe. Some light from the dopaminergic neurons
title_short The intracellular renin-angiotensin system: Friend or foe. Some light from the dopaminergic neurons
title_sort intracellular renin-angiotensin system: friend or foe. some light from the dopaminergic neurons
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7543790/
https://www.ncbi.nlm.nih.gov/pubmed/33039415
http://dx.doi.org/10.1016/j.pneurobio.2020.101919
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