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Nicotinic cholinergic system and COVID-19: In silico evaluation of nicotinic acetylcholine receptor agonists as potential therapeutic interventions

SARS-CoV-2 infection was announced as a pandemic in March 2020. Since then, several scientists have focused on the low prevalence of smokers among hospitalized COVID-19 patients. These findings led to our hypothesis that the Nicotinic Cholinergic System (NCS) plays a crucial role in the manifestatio...

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Autores principales: Alexandris, Nikolaos, Lagoumintzis, George, Chasapis, Christos T., Leonidas, Demetres D., Papadopoulos, Georgios E., Tzartos, Socrates J., Tsatsakis, Aristidis, Eliopoulos, Elias, Poulas, Konstantinos, Farsalinos, Konstantinos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7776751/
https://www.ncbi.nlm.nih.gov/pubmed/33425684
http://dx.doi.org/10.1016/j.toxrep.2020.12.013
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author Alexandris, Nikolaos
Lagoumintzis, George
Chasapis, Christos T.
Leonidas, Demetres D.
Papadopoulos, Georgios E.
Tzartos, Socrates J.
Tsatsakis, Aristidis
Eliopoulos, Elias
Poulas, Konstantinos
Farsalinos, Konstantinos
author_facet Alexandris, Nikolaos
Lagoumintzis, George
Chasapis, Christos T.
Leonidas, Demetres D.
Papadopoulos, Georgios E.
Tzartos, Socrates J.
Tsatsakis, Aristidis
Eliopoulos, Elias
Poulas, Konstantinos
Farsalinos, Konstantinos
author_sort Alexandris, Nikolaos
collection PubMed
description SARS-CoV-2 infection was announced as a pandemic in March 2020. Since then, several scientists have focused on the low prevalence of smokers among hospitalized COVID-19 patients. These findings led to our hypothesis that the Nicotinic Cholinergic System (NCS) plays a crucial role in the manifestation of COVID-19 and its severe symptoms. Molecular modeling revealed that the SARS-CoV-2 Spike glycoprotein might bind to nicotinic acetylcholine receptors (nAChRs) through a cryptic epitope homologous to snake toxins, substrates well documented and known for their affinity to the nAChRs. This binding model could provide logical explanations for the acute inflammatory disorder in patients with COVID-19, which may be linked to severe dysregulation of NCS. In this study, we present a series of complexes with cholinergic agonists that can potentially prevent SARS-CoV-2 Spike glycoprotein from binding to nAChRs, avoiding dysregulation of the NCS and moderating the symptoms and clinical manifestations of COVID-19. If our hypothesis is verified by in vitro and in vivo studies, repurposing agents currently approved for smoking cessation and neurological conditions could provide the scientific community with a therapeutic option in severe COVID-19.
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spelling pubmed-77767512021-01-07 Nicotinic cholinergic system and COVID-19: In silico evaluation of nicotinic acetylcholine receptor agonists as potential therapeutic interventions Alexandris, Nikolaos Lagoumintzis, George Chasapis, Christos T. Leonidas, Demetres D. Papadopoulos, Georgios E. Tzartos, Socrates J. Tsatsakis, Aristidis Eliopoulos, Elias Poulas, Konstantinos Farsalinos, Konstantinos Toxicol Rep Regular Article SARS-CoV-2 infection was announced as a pandemic in March 2020. Since then, several scientists have focused on the low prevalence of smokers among hospitalized COVID-19 patients. These findings led to our hypothesis that the Nicotinic Cholinergic System (NCS) plays a crucial role in the manifestation of COVID-19 and its severe symptoms. Molecular modeling revealed that the SARS-CoV-2 Spike glycoprotein might bind to nicotinic acetylcholine receptors (nAChRs) through a cryptic epitope homologous to snake toxins, substrates well documented and known for their affinity to the nAChRs. This binding model could provide logical explanations for the acute inflammatory disorder in patients with COVID-19, which may be linked to severe dysregulation of NCS. In this study, we present a series of complexes with cholinergic agonists that can potentially prevent SARS-CoV-2 Spike glycoprotein from binding to nAChRs, avoiding dysregulation of the NCS and moderating the symptoms and clinical manifestations of COVID-19. If our hypothesis is verified by in vitro and in vivo studies, repurposing agents currently approved for smoking cessation and neurological conditions could provide the scientific community with a therapeutic option in severe COVID-19. Elsevier 2020-12-19 /pmc/articles/PMC7776751/ /pubmed/33425684 http://dx.doi.org/10.1016/j.toxrep.2020.12.013 Text en © 2020 The Authors. Published by Elsevier B.V. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Regular Article
Alexandris, Nikolaos
Lagoumintzis, George
Chasapis, Christos T.
Leonidas, Demetres D.
Papadopoulos, Georgios E.
Tzartos, Socrates J.
Tsatsakis, Aristidis
Eliopoulos, Elias
Poulas, Konstantinos
Farsalinos, Konstantinos
Nicotinic cholinergic system and COVID-19: In silico evaluation of nicotinic acetylcholine receptor agonists as potential therapeutic interventions
title Nicotinic cholinergic system and COVID-19: In silico evaluation of nicotinic acetylcholine receptor agonists as potential therapeutic interventions
title_full Nicotinic cholinergic system and COVID-19: In silico evaluation of nicotinic acetylcholine receptor agonists as potential therapeutic interventions
title_fullStr Nicotinic cholinergic system and COVID-19: In silico evaluation of nicotinic acetylcholine receptor agonists as potential therapeutic interventions
title_full_unstemmed Nicotinic cholinergic system and COVID-19: In silico evaluation of nicotinic acetylcholine receptor agonists as potential therapeutic interventions
title_short Nicotinic cholinergic system and COVID-19: In silico evaluation of nicotinic acetylcholine receptor agonists as potential therapeutic interventions
title_sort nicotinic cholinergic system and covid-19: in silico evaluation of nicotinic acetylcholine receptor agonists as potential therapeutic interventions
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7776751/
https://www.ncbi.nlm.nih.gov/pubmed/33425684
http://dx.doi.org/10.1016/j.toxrep.2020.12.013
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