Εμφάνιση απλής εγγραφής

dc.creatorAlexandris N., Lagoumintzis G., Chasapis C.T., Leonidas D.D., Papadopoulos G.E., Tzartos S.J., Tsatsakis A., Eliopoulos E., Poulas K., Farsalinos K.en
dc.date.accessioned2023-01-31T07:30:50Z
dc.date.available2023-01-31T07:30:50Z
dc.date.issued2021
dc.identifier10.1016/j.toxrep.2020.12.013
dc.identifier.issn22147500
dc.identifier.urihttp://hdl.handle.net/11615/70411
dc.description.abstractSARS-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. © 2020en
dc.language.isoenen
dc.sourceToxicology Reportsen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85098484552&doi=10.1016%2fj.toxrep.2020.12.013&partnerID=40&md5=3d1d79c84fdaa5f68c61e044245de49d
dc.subjectacetylcholineen
dc.subjectcarbacholen
dc.subjectcoronavirus spike glycoproteinen
dc.subjectcytisineen
dc.subjectepibatidineen
dc.subjectgalantamineen
dc.subjectnicotinic agenten
dc.subjectsuxamethoniumen
dc.subjectvareniclineen
dc.subjectArticleen
dc.subjectbinding affinityen
dc.subjectbioinformaticsen
dc.subjectcholinergic systemen
dc.subjectcoronavirus disease 2019en
dc.subjectmolecular dockingen
dc.subjectmolecular modelen
dc.subjectprotein interactionen
dc.subjectprotein structureen
dc.subjectsequence alignmenten
dc.subjectSevere acute respiratory syndrome coronavirus 2en
dc.subjectX ray diffractionen
dc.subjectElsevier Inc.en
dc.titleNicotinic cholinergic system and COVID-19: In silico evaluation of nicotinic acetylcholine receptor agonists as potential therapeutic interventionsen
dc.typejournalArticleen


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