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Cholinergic dysfunction in COVID-19: frantic search and hoping for the best
A novel coronavirus known as severe acute respiratory syndrome coronavirus type 2 (SARS-CoV-2) is a potential cause of acute respiratory infection called coronavirus disease 2019 (COVID-19). The binding of SARS-CoV-2 with angiotensin-converting enzyme 2 (ACE2) induces a series of inflammatory cellul...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9735034/ https://www.ncbi.nlm.nih.gov/pubmed/36460816 http://dx.doi.org/10.1007/s00210-022-02346-9 |
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author | Nadwa, Eman Hassan Al-Kuraishy, Hayder M. Al-Gareeb, Ali I. Elekhnawy, Engy Albogami, Sarah M. Alorabi, Mohammed Batiha, Gaber El-Saber De Waard, Michel |
author_facet | Nadwa, Eman Hassan Al-Kuraishy, Hayder M. Al-Gareeb, Ali I. Elekhnawy, Engy Albogami, Sarah M. Alorabi, Mohammed Batiha, Gaber El-Saber De Waard, Michel |
author_sort | Nadwa, Eman Hassan |
collection | PubMed |
description | A novel coronavirus known as severe acute respiratory syndrome coronavirus type 2 (SARS-CoV-2) is a potential cause of acute respiratory infection called coronavirus disease 2019 (COVID-19). The binding of SARS-CoV-2 with angiotensin-converting enzyme 2 (ACE2) induces a series of inflammatory cellular events with cytopathic effects leading to cell injury and hyperinflammation. Severe SARS-CoV-2 infection may lead to dysautonomia and sympathetic storm due to dysfunction of the autonomic nervous system (ANS). Therefore, this review aimed to elucidate the critical role of the cholinergic system (CS) in SARS-CoV-2 infection. The CS forms a multi-faceted network performing diverse functions in the body due to its distribution in the neuronal and non-neuronal cells. Acetylcholine (ACh) acts on two main types of receptors which are nicotinic receptors (NRs) and muscarinic receptors (MRs). NRs induce T cell anergy with impairment of antigen-mediated signal transduction. Nicotine through activation of T cell NRs inhibits the expression and release of the pro-inflammatory cytokines. NRs play important anti-inflammatory effects while MRs promote inflammation by inducing the release of pro-inflammatory cytokines. SARS-CoV-2 infection can affect the morphological and functional stability of CS through the disruption of cholinergic receptors. SARS-CoV-2 spike protein is similar to neurotoxins, which can bind to nicotinic acetylcholine receptors (nAChR) in the ANS and brain. Therefore, cholinergic receptors mainly nAChR and related cholinergic agonists may affect the pathogenesis of SARS-CoV-2 infection. Cholinergic dysfunction in COVID-19 is due to dysregulation of nAChR by SARS-CoV-2 promoting the central sympathetic drive with the development of the sympathetic storm. As well, nAChR activators through interaction with diverse signaling pathways can reduce the risk of inflammatory disorders in COVID-19. In addition, nAChR activators may mitigate endothelial dysfunction (ED), oxidative stress (OS), and associated coagulopathy in COVID-19. Similarly, nAChR activators may improve OS, inflammatory changes, and cytokine storm in COVID-19. Therefore, nAChR activators like varenicline in virtue of its anti-inflammatory and anti-oxidant effects with direct anti-SARS-CoV-2 effect could be effective in the management of COVID-19. |
format | Online Article Text |
id | pubmed-9735034 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-97350342022-12-12 Cholinergic dysfunction in COVID-19: frantic search and hoping for the best Nadwa, Eman Hassan Al-Kuraishy, Hayder M. Al-Gareeb, Ali I. Elekhnawy, Engy Albogami, Sarah M. Alorabi, Mohammed Batiha, Gaber El-Saber De Waard, Michel Naunyn Schmiedebergs Arch Pharmacol Review A novel coronavirus known as severe acute respiratory syndrome coronavirus type 2 (SARS-CoV-2) is a potential cause of acute respiratory infection called coronavirus disease 2019 (COVID-19). The binding of SARS-CoV-2 with angiotensin-converting enzyme 2 (ACE2) induces a series of inflammatory cellular events with cytopathic effects leading to cell injury and hyperinflammation. Severe SARS-CoV-2 infection may lead to dysautonomia and sympathetic storm due to dysfunction of the autonomic nervous system (ANS). Therefore, this review aimed to elucidate the critical role of the cholinergic system (CS) in SARS-CoV-2 infection. The CS forms a multi-faceted network performing diverse functions in the body due to its distribution in the neuronal and non-neuronal cells. Acetylcholine (ACh) acts on two main types of receptors which are nicotinic receptors (NRs) and muscarinic receptors (MRs). NRs induce T cell anergy with impairment of antigen-mediated signal transduction. Nicotine through activation of T cell NRs inhibits the expression and release of the pro-inflammatory cytokines. NRs play important anti-inflammatory effects while MRs promote inflammation by inducing the release of pro-inflammatory cytokines. SARS-CoV-2 infection can affect the morphological and functional stability of CS through the disruption of cholinergic receptors. SARS-CoV-2 spike protein is similar to neurotoxins, which can bind to nicotinic acetylcholine receptors (nAChR) in the ANS and brain. Therefore, cholinergic receptors mainly nAChR and related cholinergic agonists may affect the pathogenesis of SARS-CoV-2 infection. Cholinergic dysfunction in COVID-19 is due to dysregulation of nAChR by SARS-CoV-2 promoting the central sympathetic drive with the development of the sympathetic storm. As well, nAChR activators through interaction with diverse signaling pathways can reduce the risk of inflammatory disorders in COVID-19. In addition, nAChR activators may mitigate endothelial dysfunction (ED), oxidative stress (OS), and associated coagulopathy in COVID-19. Similarly, nAChR activators may improve OS, inflammatory changes, and cytokine storm in COVID-19. Therefore, nAChR activators like varenicline in virtue of its anti-inflammatory and anti-oxidant effects with direct anti-SARS-CoV-2 effect could be effective in the management of COVID-19. Springer Berlin Heidelberg 2022-12-03 2023 /pmc/articles/PMC9735034/ /pubmed/36460816 http://dx.doi.org/10.1007/s00210-022-02346-9 Text en © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2022, Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. 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 Nadwa, Eman Hassan Al-Kuraishy, Hayder M. Al-Gareeb, Ali I. Elekhnawy, Engy Albogami, Sarah M. Alorabi, Mohammed Batiha, Gaber El-Saber De Waard, Michel Cholinergic dysfunction in COVID-19: frantic search and hoping for the best |
title | Cholinergic dysfunction in COVID-19: frantic search and hoping for the best |
title_full | Cholinergic dysfunction in COVID-19: frantic search and hoping for the best |
title_fullStr | Cholinergic dysfunction in COVID-19: frantic search and hoping for the best |
title_full_unstemmed | Cholinergic dysfunction in COVID-19: frantic search and hoping for the best |
title_short | Cholinergic dysfunction in COVID-19: frantic search and hoping for the best |
title_sort | cholinergic dysfunction in covid-19: frantic search and hoping for the best |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9735034/ https://www.ncbi.nlm.nih.gov/pubmed/36460816 http://dx.doi.org/10.1007/s00210-022-02346-9 |
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