Therapeutic potential of melatonin and melatonergic drugs on K18-hACE2 mice infected with SARS-CoV-2.
Erika CeconCharlotte IzabelleSophie Le PoderFernando RealAiwei ZhuLy TuMaria-Rosa GhignaBernard KlonjkowskiMorgane BomselRalf JockersJulie DamPublished in: Journal of pineal research (2021)
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.
Keyphrases
- sars cov
- respiratory syndrome coronavirus
- coronavirus disease
- clinical trial
- high fat diet induced
- type iii
- drug induced
- risk assessment
- endothelial cells
- gene expression
- randomized controlled trial
- physical activity
- type diabetes
- depressive symptoms
- emergency department
- mesenchymal stem cells
- bone marrow
- quantum dots
- early onset
- free survival
- study protocol
- sleep quality
- binding protein
- cell therapy
- angiotensin converting enzyme
- smoking cessation