Institut Cochin, INSERM, CNRS, Université de Paris, Paris, France.
UMR Virologie, INRAE, ANSES, École Nationale Vétérinaire d'Alfort, Maisons-Alfort, France.
J Pineal Res. 2022 Jan;72(1):e12772. doi: 10.1111/jpi.12772. Epub 2021 Oct 15.
As the COVID-19 pandemic grows, several therapeutic candidates are being tested or undergoing clinical trials. Although prophylactic vaccination against SARS-CoV-2 infection has been shown to be effective, no definitive treatment exists to date in the event of infection. The rapid spread of infection by SARS-CoV-2 and its variants fully warrants the continued evaluation of drug treatments for COVID-19, especially in the context of repurposing of already available and safe drugs. Here, we explored the therapeutic potential of melatonin and melatonergic compounds in attenuating COVID-19 pathogenesis in mice expressing human ACE2 receptor (K18-hACE2), strongly susceptible to SARS-CoV-2 infection. Daily administration of melatonin, agomelatine, or ramelteon delays the occurrence of severe clinical outcome with improvement of survival, especially with high melatonin dose. Although no changes in most lung inflammatory cytokines are observed, treatment with melatonergic compounds limits the exacerbated local lung production of type I and type III interferons, which is likely associated with the observed improved symptoms in treated mice. The promising results from this preclinical study should encourage studies examining the benefits of repurposing melatonergic drugs to treat COVID-19 and related diseases in humans.
随着 COVID-19 大流行的发展,几种治疗候选药物正在进行测试或临床试验。尽管预防 SARS-CoV-2 感染的疫苗已被证明有效,但迄今为止,在感染的情况下,尚无明确的治疗方法。SARS-CoV-2 及其变体的迅速传播充分证明了需要继续评估 COVID-19 的药物治疗方法,特别是在重新利用已经可用和安全的药物方面。在这里,我们研究了褪黑素和褪黑素能化合物在减轻表达人 ACE2 受体 (K18-hACE2) 的小鼠 COVID-19 发病机制方面的治疗潜力,这些小鼠对 SARS-CoV-2 感染高度敏感。褪黑素、阿戈美拉汀或雷美替胺的每日给药可延迟严重临床结果的发生,并提高存活率,尤其是高剂量褪黑素。尽管大多数肺部炎症细胞因子没有变化,但褪黑素能化合物的治疗可限制局部肺部产生 I 型和 III 型干扰素的加剧,这可能与观察到的治疗小鼠症状改善有关。这项临床前研究的有希望结果应鼓励研究重新利用褪黑素药物治疗 COVID-19 和相关人类疾病的益处。