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Diabetes and inflammatory diseases: An overview from the perspective of Ca(2+)/3'-5'-cyclic adenosine monophosphate signaling

A large amount of evidence has supported a clinical link between diabetes and inflammatory diseases, e.g., cancer, dementia, and hypertension. In addition, it is also suggested that dysregulations related to Ca(2+ )signaling could link these diseases, in addition to 3'-5'-cyclic adenosine...

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Autor principal: Bergantin, Leandro Bueno
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8192245/
https://www.ncbi.nlm.nih.gov/pubmed/34168726
http://dx.doi.org/10.4239/wjd.v12.i6.767
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author Bergantin, Leandro Bueno
author_facet Bergantin, Leandro Bueno
author_sort Bergantin, Leandro Bueno
collection PubMed
description A large amount of evidence has supported a clinical link between diabetes and inflammatory diseases, e.g., cancer, dementia, and hypertension. In addition, it is also suggested that dysregulations related to Ca(2+ )signaling could link these diseases, in addition to 3'-5'-cyclic adenosine monophosphate (cAMP) signaling pathways. Thus, revealing this interplay between diabetes and inflammatory diseases may provide novel insights into the pathogenesis of these diseases. Publications involving signaling pathways related to Ca(2+) and cAMP, inflammation, diabetes, dementia, cancer, and hypertension (alone or combined) were collected by searching PubMed and EMBASE. Both signaling pathways, Ca(2+) and cAMP signaling, control the release of neurotransmitters and hormones, in addition to neurodegeneration, and tumor growth. Furthermore, there is a clear relationship between Ca(2+) signaling, e.g., increased Ca(2+) signals, and inflammatory responses. cAMP also regulates pro- and anti-inflammatory responses. Due to the experience of our group in this field, this article discusses the role of Ca(2+) and cAMP signaling in the correlation between diabetes and inflammatory diseases, including its pharmacological implications. As a novelty, this article also includes: (1) A timeline of the major events in Ca(2+)/cAMP signaling; and (2) As coronavirus disease 2019 (COVID-19) is an emerging and rapidly evolving situation, this article also discusses recent reports on the role of Ca(2+) channel blockers for preventing Ca(2+) signaling disruption due to COVID-19, including the correlation between COVID-19 and diabetes.
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spelling pubmed-81922452021-06-23 Diabetes and inflammatory diseases: An overview from the perspective of Ca(2+)/3'-5'-cyclic adenosine monophosphate signaling Bergantin, Leandro Bueno World J Diabetes Minireviews A large amount of evidence has supported a clinical link between diabetes and inflammatory diseases, e.g., cancer, dementia, and hypertension. In addition, it is also suggested that dysregulations related to Ca(2+ )signaling could link these diseases, in addition to 3'-5'-cyclic adenosine monophosphate (cAMP) signaling pathways. Thus, revealing this interplay between diabetes and inflammatory diseases may provide novel insights into the pathogenesis of these diseases. Publications involving signaling pathways related to Ca(2+) and cAMP, inflammation, diabetes, dementia, cancer, and hypertension (alone or combined) were collected by searching PubMed and EMBASE. Both signaling pathways, Ca(2+) and cAMP signaling, control the release of neurotransmitters and hormones, in addition to neurodegeneration, and tumor growth. Furthermore, there is a clear relationship between Ca(2+) signaling, e.g., increased Ca(2+) signals, and inflammatory responses. cAMP also regulates pro- and anti-inflammatory responses. Due to the experience of our group in this field, this article discusses the role of Ca(2+) and cAMP signaling in the correlation between diabetes and inflammatory diseases, including its pharmacological implications. As a novelty, this article also includes: (1) A timeline of the major events in Ca(2+)/cAMP signaling; and (2) As coronavirus disease 2019 (COVID-19) is an emerging and rapidly evolving situation, this article also discusses recent reports on the role of Ca(2+) channel blockers for preventing Ca(2+) signaling disruption due to COVID-19, including the correlation between COVID-19 and diabetes. Baishideng Publishing Group Inc 2021-06-15 2021-06-15 /pmc/articles/PMC8192245/ /pubmed/34168726 http://dx.doi.org/10.4239/wjd.v12.i6.767 Text en ©The Author(s) 2021. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/Licenses/by-nc/4.0/
spellingShingle Minireviews
Bergantin, Leandro Bueno
Diabetes and inflammatory diseases: An overview from the perspective of Ca(2+)/3'-5'-cyclic adenosine monophosphate signaling
title Diabetes and inflammatory diseases: An overview from the perspective of Ca(2+)/3'-5'-cyclic adenosine monophosphate signaling
title_full Diabetes and inflammatory diseases: An overview from the perspective of Ca(2+)/3'-5'-cyclic adenosine monophosphate signaling
title_fullStr Diabetes and inflammatory diseases: An overview from the perspective of Ca(2+)/3'-5'-cyclic adenosine monophosphate signaling
title_full_unstemmed Diabetes and inflammatory diseases: An overview from the perspective of Ca(2+)/3'-5'-cyclic adenosine monophosphate signaling
title_short Diabetes and inflammatory diseases: An overview from the perspective of Ca(2+)/3'-5'-cyclic adenosine monophosphate signaling
title_sort diabetes and inflammatory diseases: an overview from the perspective of ca(2+)/3'-5'-cyclic adenosine monophosphate signaling
topic Minireviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8192245/
https://www.ncbi.nlm.nih.gov/pubmed/34168726
http://dx.doi.org/10.4239/wjd.v12.i6.767
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