Department of Neuroscience Rita Levi Montalcini, University of Turin, Turin, Italy.
University of Turin, Neuroscience Institute of the Cavalieri-Ottolenghi Foundation, Orbassano (TORINO), Italy.
Br J Pharmacol. 2020 Nov;177(21):4921-4930. doi: 10.1111/bph.15229. Epub 2020 Aug 26.
COVID-19, the illness caused by SARS-CoV-2, has a wide-ranging clinical spectrum that, in the worst-case scenario, involves a rapid progression to severe acute respiratory syndrome and death. Epidemiological data show that obesity and diabetes are among the main risk factors associated with high morbidity and mortality. The increased susceptibility to SARS-CoV-2 infection documented in obesity-related metabolic derangements argues for initial defects in defence mechanisms, most likely due to an elevated systemic metabolic inflammation ("metaflammation"). The NLRP3 inflammasome is a master regulator of metaflammation and has a pivotal role in the pathophysiology of either obesity or diabetes. Here, we discuss the most recent findings suggesting contribution of NLRP3 inflammasome to the increase in complications in COVID-19 patients with diabesity. We also review current pharmacological strategies for COVID-19, focusing on treatments whose efficacy could be due, at least in part, to interference with the activation of the NLRP3 inflammasome. LINKED ARTICLES: This article is part of a themed issue on The Pharmacology of COVID-19. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v177.21/issuetoc.
新型冠状病毒病(COVID-19)是由严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)引起的一种疾病,其临床表现广泛,在最坏的情况下,病情迅速进展为严重急性呼吸综合征,并导致死亡。流行病学数据表明,肥胖和糖尿病是与高发病率和死亡率相关的主要危险因素之一。肥胖相关代谢紊乱导致对 SARS-CoV-2 感染的易感性增加,这表明防御机制最初存在缺陷,很可能是由于全身性代谢炎症(“代谢性炎症”)升高。NLRP3 炎性体是代谢性炎症的主要调节因子,在肥胖或糖尿病的病理生理学中具有关键作用。在这里,我们讨论了最近的发现,这些发现表明 NLRP3 炎性体参与了合并糖尿病的 COVID-19 患者并发症的增加。我们还回顾了 COVID-19 的当前药理学策略,重点关注那些疗效至少部分归因于干扰 NLRP3 炎性体激活的治疗方法。相关文章:本文是关于 COVID-19 药理学的专题问题的一部分。要查看该部分中的其他文章,请访问 http://onlinelibrary.wiley.com/doi/10.1111/bph.v177.21/issuetoc.