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双重抑制 CB 受体和 iNOS,作为治疗急性和长新冠的潜在新策略。

Dual inhibition of CB receptors and iNOS, as a potential novel approach to the pharmacological management of acute and long COVID-19.

机构信息

Section on Fibrotic Disorders, National Institute on Alcohol Abuse and Alcoholism (NIAAA), National Institutes of Health (NIH), Bethesda, Maryland, USA.

Section on Medicinal Chemistry, National Institute on Alcohol Abuse and Alcoholism (NIAAA), National Institutes of Health (NIH), Bethesda, Maryland, USA.

出版信息

Br J Pharmacol. 2022 May;179(10):2121-2127. doi: 10.1111/bph.15461. Epub 2021 Apr 17.

Abstract

COVID-19 (SARS-CoV-2) causes multiple inflammatory complications, resulting not only in severe lung inflammation but also harm to other organs. Although the current focus is on the management of acute COVID-19, there is growing concern about long-term effects of COVID-19 (Long Covid), such as fibroproliferative changes in the lung, heart and kidney. Therefore, the identification of therapeutic targets not only for the management of acute COVID-19 but also for preventing Long Covid are needed, and would mitigate against long-lasting health burden and economic costs, in addition to saving lives. COVID-19 induces pathological changes via multiple pathways, which could be targeted simultaneously for optimal effect. We discuss the potential pathologic function of increased activity of the endocannabinoid/CB receptor system and inducible NO synthase (iNOS). We advocate a polypharmacology approach, wherein a single chemical entity simultaneously interacts with CB receptors and iNOS causing inhibition, as a potential therapeutic strategy for COVID-19-related health complications. LINKED ARTICLES: This article is part of a themed issue on The second wave: are we any closer to efficacious pharmacotherapy for COVID 19? (BJP 75th Anniversary). To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v179.10/issuetoc.

摘要

新型冠状病毒(SARS-CoV-2)引发多种炎症并发症,不仅导致严重肺部炎症,还对其他器官造成损伤。虽然目前的重点是急性新型冠状病毒的管理,但人们越来越关注新型冠状病毒(长新冠)的长期影响,例如肺部、心脏和肾脏的纤维增生性变化。因此,不仅需要确定治疗靶点以管理急性新型冠状病毒,还需要预防长新冠,从而减轻长期健康负担和经济成本,同时挽救生命。新型冠状病毒通过多种途径引起病理变化,可以同时针对这些途径进行靶向治疗以达到最佳效果。我们讨论了内源性大麻素/CB 受体系统和诱导型一氧化氮合酶(iNOS)活性增加的潜在病理功能。我们提倡采用多药理学方法,即单一化学实体同时与 CB 受体和 iNOS 相互作用,从而抑制它们,作为治疗新型冠状病毒相关健康并发症的潜在治疗策略。相关文章:本文是关于“第二波:我们离有效的新型冠状病毒药理学治疗更近了吗?”的专题文章的一部分(BJP 75 周年纪念)。要查看本节中的其他文章,请访问 http://onlinelibrary.wiley.com/doi/10.1111/bph.v179.10/issuetoc.

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