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Med Hypotheses ; 143: 110197, 2020 Oct.
Article in English | MEDLINE | ID: covidwho-716873

ABSTRACT

Coronavirus disease 2019 (COVID-19) may have a metabolic origin given strong links with risk factors such as lipids and glucose and co-morbidities such as obesity and type 2 diabetes mellitus. The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein mediates viral cellular entry via the ACE2 receptor. The cytoplasmic tail of this spike protein is heavily palmitoylated. Emerging studies suggest that SARS-CoV-2 alters lipid metabolism in the lung epithelial cells by modulating peroxisome proliferator-activated receptor alpha (PPARα), possibly contributing to lipotoxicity, inflammation and untoward respiratory effects. Disruption of this process may affect palmitoylation of SARS-CoV spike protein and thus infectivity and viral assembly. COVID-19 is also increasingly being recognized as a vascular disease, with several studies noting prominent systemic endothelial dysfunction. The pathogenesis of endothelial dysfunction may also be linked to COVID-19-mediated metabolic and inflammatory effects. Herein, exercise will be compared to fenofibrate as a possible therapeutic strategy to bolster resilience against (and help manage recovery from) COVID-19. This paper will explore the hypothesis that exercise may be a useful adjuvant in a setting of COVID-19 management/rehabilitation due to its effects on PPARα and vascular endothelial function.


Subject(s)
Coronavirus Infections/therapy , Exercise Therapy/methods , PPAR alpha/metabolism , Pneumonia, Viral/therapy , Spike Glycoprotein, Coronavirus/metabolism , Betacoronavirus , COVID-19 , Comorbidity , Coronavirus Infections/drug therapy , Cytoplasm/metabolism , Diabetes Mellitus, Type 2/complications , Exercise , Fenofibrate/chemistry , Humans , Inflammation , Lipid Metabolism , Lipoylation , Lung/metabolism , Obesity/complications , Pandemics , SARS-CoV-2 , COVID-19 Drug Treatment
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