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褪黑素可能降低 COVID-19 和其他 RNA 病毒感染的风险并有助于治疗。

Melatonin may decrease risk for and aid treatment of COVID-19 and other RNA viral infections.

机构信息

Department of Preventive Cardiology, Saint Luke's Mid America Heart Institute, Kansas City, Missouri, USA

Catalytic Longevity, Encinitas, California, USA.

出版信息

Open Heart. 2021 Mar;8(1). doi: 10.1136/openhrt-2020-001568.

Abstract

A recent retrospective study has provided evidence that COVID-19 infection may be notably less common in those using supplemental melatonin. It is suggested that this phenomenon may reflect the fact that, via induction of silent information regulator 1 (Sirt1), melatonin can upregulate K63 polyubiquitination of the mitochondrial antiviral-signalling protein, thereby boosting virally mediated induction of type 1 interferons. Moreover, Sirt1 may enhance the antiviral efficacy of type 1 interferons by preventing hyperacetylation of high mobility group box 1 (HMGB1), enabling its retention in the nucleus, where it promotes transcription of interferon-inducible genes. This nuclear retention of HMGB1 may also be a mediator of the anti-inflammatory effect of melatonin therapy in COVID-19-complementing melatonin's suppression of nuclear factor kappa B activity and upregulation of nuclear factor erythroid 2-related factor 2. If these speculations are correct, a nutraceutical regimen including vitamin D, zinc and melatonin supplementation may have general utility for the prevention and treatment of RNA virus infections, such as COVID-19 and influenza.

摘要

一项最近的回顾性研究提供了证据,表明 COVID-19 感染在使用补充褪黑素的人群中明显较少见。这一现象可能反映了这样一个事实,即褪黑素通过诱导沉默信息调节因子 1(Sirt1),可以上调线粒体抗病毒信号蛋白的 K63 多聚泛素化,从而增强病毒介导的 1 型干扰素的诱导。此外,Sirt1 可以通过防止高迁移率族蛋白 1(HMGB1)的过度乙酰化来增强 1 型干扰素的抗病毒功效,使 HMGB1 保留在核内,从而促进干扰素诱导基因的转录。HMGB1 的核内保留也可能是褪黑素治疗 COVID-19 中抗炎作用的介导物,补充褪黑素抑制核因子 kappa B 活性和上调核因子红细胞 2 相关因子 2。如果这些推测是正确的,那么包括维生素 D、锌和褪黑素补充剂在内的营养疗法可能对预防和治疗 RNA 病毒感染(如 COVID-19 和流感)具有普遍的效用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9d4/7985934/8237831c1b6b/openhrt-2020-001568f01.jpg

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