Alexandris Nikolaos, Lagoumintzis George, Chasapis Christos T, Leonidas Demetres D, Papadopoulos Georgios E, Tzartos Socrates J, Tsatsakis Aristidis, Eliopoulos Elias, Poulas Konstantinos, Farsalinos Konstantinos
Laboratory of Molecular Biology and Immunology, Department of Pharmacy, University of Patras, 26500, Rio-Patras, Greece.
Institute of Research and Innovation - IRIS, Patras Science Park SA, 26500 Patras, Greece.
Toxicol Rep. 2020 Dec 19;8:73-83. doi: 10.1016/j.toxrep.2020.12.013. eCollection 2021.
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 and studies, repurposing agents currently approved for smoking cessation and neurological conditions could provide the scientific community with a therapeutic option in severe COVID-19.
2020年3月,严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染被宣布为全球大流行。从那时起,一些科学家专注于住院的2019冠状病毒病(COVID-19)患者中吸烟者比例较低这一现象。这些发现促使我们提出一个假设,即烟碱胆碱能系统(NCS)在COVID-19的表现及其严重症状中起关键作用。分子建模显示,SARS-CoV-2刺突糖蛋白可能通过一个与蛇毒素同源的隐蔽表位与烟碱型乙酰胆碱受体(nAChRs)结合,蛇毒素是有充分文献记载且以其对nAChRs的亲和力而闻名的底物。这种结合模型可以为COVID-19患者的急性炎症紊乱提供合理的解释,这可能与NCS的严重失调有关。在本研究中,我们展示了一系列与胆碱能激动剂形成的复合物,这些复合物可能会阻止SARS-CoV-2刺突糖蛋白与nAChRs结合,避免NCS失调,并减轻COVID-19的症状和临床表现。如果我们的假设得到[具体研究]和[具体研究]的验证,重新利用目前已获批用于戒烟和治疗神经疾病的药物,可为科学界提供一种针对重症COVID-19的治疗选择。