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dc.contributor.authorAlkhayyat, Shadi Salem
dc.contributor.authorAl-kuraishy, Hayder M.
dc.contributor.authorAl-Gareeb, Ali I.
dc.contributor.authorEl-Bouseary, Maisra M.
dc.contributor.authorAboKamer, Amal M.
dc.contributor.authorBatiha, Gaber El-Saber
dc.contributor.authorSimal Gándara, Jesús 
dc.date.accessioned2023-03-21T10:52:45Z
dc.date.available2023-03-21T10:52:45Z
dc.date.issued2022-08-08
dc.identifier.citationInflammation Research, 71, 1159-1167 (2022)spa
dc.identifier.issn10233830
dc.identifier.issn1420908X
dc.identifier.urihttp://hdl.handle.net/11093/4640
dc.descriptionFinanciado para publicación en acceso aberto: Universidade de Vigo/CISUG
dc.description.abstractIntroduction Fenofbrate is an agonist of peroxisome proliferator activated receptor alpha (PPAR-α), that possesses antiinfammatory, antioxidant, and anti-thrombotic properties. Fenofbrate is efective against a variety of viral infections and diferent infammatory disorders. Therefore, the aim of critical review was to overview the potential role of fenofbrate in the pathogenesis of SARS-CoV-2 and related complications. Results By destabilizing SARS-CoV-2 spike protein and preventing it from binding angiotensin-converting enzyme 2 (ACE2), a receptor for SARS-CoV-2 entry, fenofbrate can reduce SARS-CoV-2 entry in human cells Fenofbrate also suppresses infammatory signaling pathways, which decreases SARS-CoV-2 infection-related infammatory alterations. In conclusion, fenofbrate anti-infammatory, antioxidant, and antithrombotic capabilities may help to minimize the infammatory and thrombotic consequences associated with SARSCoV-2 infection. Through attenuating the interaction between SARS-CoV-2 and ACE2, fenofbrate can directly reduce the risk of SARS-CoV-2 infection. Conclusions As a result, fenofbrate could be a potential treatment approach for COVID-19 control.en
dc.language.isoengspa
dc.publisherInflammation Researchspa
dc.rights© 2022, The Author(s), under exclusive licence to Springer Nature Switzerland AG
dc.titleFenofibrate for COVID-19 and related complications as an approach to improve treatment outcomes: the missed key for Holy Grailen
dc.typearticlespa
dc.rights.accessRightsopenAccessspa
dc.identifier.doi10.1007/s00011-022-01615-w
dc.identifier.editorhttps://link.springer.com/10.1007/s00011-022-01615-wspa
dc.publisher.departamentoQuímica analítica e alimentariaspa
dc.publisher.grupoinvestigacionInvestigacións Agrarias e Alimentariasspa
dc.subject.unesco3209.90 Farmacología Experimentalspa
dc.subject.unesco3202 Epidemiologíaspa
dc.subject.unesco2302 Bioquímicaspa
dc.date.updated2023-03-21T10:51:21Z
dc.computerCitationpub_title=Inflammation Research|volume=71|journal_number=|start_pag=1159|end_pag=1167spa


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