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Involvement of dopaminergic signaling in the cross talk between the renin-angiotensin system and inflammation

The renin-angiotensin system (RAS) is a fundamental regulator of blood pressure and has emerged as an important player in the control of inflammatory processes. Accordingly, imbalance on RAS components either systemically or locally might trigger the development of inflammatory disorders by affectin...

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Autores principales: Campos, Javier, Pacheco, Rodrigo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7526080/
https://www.ncbi.nlm.nih.gov/pubmed/32997225
http://dx.doi.org/10.1007/s00281-020-00819-8
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author Campos, Javier
Pacheco, Rodrigo
author_facet Campos, Javier
Pacheco, Rodrigo
author_sort Campos, Javier
collection PubMed
description The renin-angiotensin system (RAS) is a fundamental regulator of blood pressure and has emerged as an important player in the control of inflammatory processes. Accordingly, imbalance on RAS components either systemically or locally might trigger the development of inflammatory disorders by affecting immune cells. At the same time, alterations in the dopaminergic system have been consistently involved in the physiopathology of inflammatory disorders. Accordingly, the interaction between the RAS and the dopaminergic system has been studied in the context of inflammation of the central nervous system (CNS), kidney, and intestine, where they exert antagonistic actions in the regulation of the immune system. In this review, we summarized, integrated, and discussed the cross talk of the dopaminergic system and the RAS in the regulation of inflammatory pathologies, including neurodegenerative disorders, such as Parkinson’s disease. We analyzed the molecular mechanisms underlying the interaction between both systems in the CNS and in systemic pathologies. Moreover, we also analyzed the impact of the commensal microbiota in the regulation of RAS and dopaminergic system and how it is involved in inflammatory disorders. Furthermore, we summarized the therapeutic approaches that have yielded positive results in preclinical or clinical studies regarding the use of drugs targeting the RAS and dopaminergic system for the treatment of inflammatory conditions. Further understanding of the molecular and cellular regulation of the RAS-dopaminergic cross talk should allow the formulation of new therapies consisting of novel drugs and/or repurposing already existing drugs, alone or in combination, for the treatment of inflammatory disorders.
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spelling pubmed-75260802020-10-01 Involvement of dopaminergic signaling in the cross talk between the renin-angiotensin system and inflammation Campos, Javier Pacheco, Rodrigo Semin Immunopathol Review The renin-angiotensin system (RAS) is a fundamental regulator of blood pressure and has emerged as an important player in the control of inflammatory processes. Accordingly, imbalance on RAS components either systemically or locally might trigger the development of inflammatory disorders by affecting immune cells. At the same time, alterations in the dopaminergic system have been consistently involved in the physiopathology of inflammatory disorders. Accordingly, the interaction between the RAS and the dopaminergic system has been studied in the context of inflammation of the central nervous system (CNS), kidney, and intestine, where they exert antagonistic actions in the regulation of the immune system. In this review, we summarized, integrated, and discussed the cross talk of the dopaminergic system and the RAS in the regulation of inflammatory pathologies, including neurodegenerative disorders, such as Parkinson’s disease. We analyzed the molecular mechanisms underlying the interaction between both systems in the CNS and in systemic pathologies. Moreover, we also analyzed the impact of the commensal microbiota in the regulation of RAS and dopaminergic system and how it is involved in inflammatory disorders. Furthermore, we summarized the therapeutic approaches that have yielded positive results in preclinical or clinical studies regarding the use of drugs targeting the RAS and dopaminergic system for the treatment of inflammatory conditions. Further understanding of the molecular and cellular regulation of the RAS-dopaminergic cross talk should allow the formulation of new therapies consisting of novel drugs and/or repurposing already existing drugs, alone or in combination, for the treatment of inflammatory disorders. Springer Berlin Heidelberg 2020-09-30 2020 /pmc/articles/PMC7526080/ /pubmed/32997225 http://dx.doi.org/10.1007/s00281-020-00819-8 Text en © Springer-Verlag GmbH Germany, part of Springer Nature 2020 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Review
Campos, Javier
Pacheco, Rodrigo
Involvement of dopaminergic signaling in the cross talk between the renin-angiotensin system and inflammation
title Involvement of dopaminergic signaling in the cross talk between the renin-angiotensin system and inflammation
title_full Involvement of dopaminergic signaling in the cross talk between the renin-angiotensin system and inflammation
title_fullStr Involvement of dopaminergic signaling in the cross talk between the renin-angiotensin system and inflammation
title_full_unstemmed Involvement of dopaminergic signaling in the cross talk between the renin-angiotensin system and inflammation
title_short Involvement of dopaminergic signaling in the cross talk between the renin-angiotensin system and inflammation
title_sort involvement of dopaminergic signaling in the cross talk between the renin-angiotensin system and inflammation
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7526080/
https://www.ncbi.nlm.nih.gov/pubmed/32997225
http://dx.doi.org/10.1007/s00281-020-00819-8
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