Cargando…
Nrf2 Activator PB125(®) as a Potential Therapeutic Agent against COVID-19
Nrf2 is a transcription factor that regulates cellular redox balance and the expression of a wide array of genes involved in immunity and inflammation, including antiviral actions. Nrf2 activity declines with age, making the elderly more susceptible to oxidative stress-mediated diseases, which inclu...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7346195/ https://www.ncbi.nlm.nih.gov/pubmed/32545518 http://dx.doi.org/10.3390/antiox9060518 |
_version_ | 1783556355817209856 |
---|---|
author | McCord, Joe M. Hybertson, Brooks M. Cota-Gomez, Adela Geraci, Kara P. Gao, Bifeng |
author_facet | McCord, Joe M. Hybertson, Brooks M. Cota-Gomez, Adela Geraci, Kara P. Gao, Bifeng |
author_sort | McCord, Joe M. |
collection | PubMed |
description | Nrf2 is a transcription factor that regulates cellular redox balance and the expression of a wide array of genes involved in immunity and inflammation, including antiviral actions. Nrf2 activity declines with age, making the elderly more susceptible to oxidative stress-mediated diseases, which include type 2 diabetes, chronic inflammation, and viral infections. Published evidence suggests that Nrf2 activity may regulate important mechanisms affecting viral susceptibility and replication. We examined gene expression levels by GeneChip microarray and by RNA-seq assays. We found that the potent Nrf2-activating composition PB125(®) downregulates ACE2 and TMPRSS2 mRNA expression in human liver-derived HepG2 cells. ACE2 is a surface receptor and TMPRSS2 activates the spike protein for SARS-CoV-2 entry into host cells. Furthermore, in endotoxin-stimulated primary human pulmonary artery endothelial cells, we report the marked downregulation by PB125 of 36 genes encoding cytokines. These include IL-1-beta, IL-6, TNF-α, the cell adhesion molecules ICAM-1, VCAM-1, and E-selectin, and a group of IFN-γ-induced genes. Many of these cytokines have been specifically identified in the “cytokine storm” observed in fatal cases of COVID-19, suggesting that Nrf2 activation may significantly decrease the intensity of the storm. |
format | Online Article Text |
id | pubmed-7346195 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-73461952020-07-14 Nrf2 Activator PB125(®) as a Potential Therapeutic Agent against COVID-19 McCord, Joe M. Hybertson, Brooks M. Cota-Gomez, Adela Geraci, Kara P. Gao, Bifeng Antioxidants (Basel) Article Nrf2 is a transcription factor that regulates cellular redox balance and the expression of a wide array of genes involved in immunity and inflammation, including antiviral actions. Nrf2 activity declines with age, making the elderly more susceptible to oxidative stress-mediated diseases, which include type 2 diabetes, chronic inflammation, and viral infections. Published evidence suggests that Nrf2 activity may regulate important mechanisms affecting viral susceptibility and replication. We examined gene expression levels by GeneChip microarray and by RNA-seq assays. We found that the potent Nrf2-activating composition PB125(®) downregulates ACE2 and TMPRSS2 mRNA expression in human liver-derived HepG2 cells. ACE2 is a surface receptor and TMPRSS2 activates the spike protein for SARS-CoV-2 entry into host cells. Furthermore, in endotoxin-stimulated primary human pulmonary artery endothelial cells, we report the marked downregulation by PB125 of 36 genes encoding cytokines. These include IL-1-beta, IL-6, TNF-α, the cell adhesion molecules ICAM-1, VCAM-1, and E-selectin, and a group of IFN-γ-induced genes. Many of these cytokines have been specifically identified in the “cytokine storm” observed in fatal cases of COVID-19, suggesting that Nrf2 activation may significantly decrease the intensity of the storm. MDPI 2020-06-12 /pmc/articles/PMC7346195/ /pubmed/32545518 http://dx.doi.org/10.3390/antiox9060518 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article McCord, Joe M. Hybertson, Brooks M. Cota-Gomez, Adela Geraci, Kara P. Gao, Bifeng Nrf2 Activator PB125(®) as a Potential Therapeutic Agent against COVID-19 |
title | Nrf2 Activator PB125(®) as a Potential Therapeutic Agent against COVID-19 |
title_full | Nrf2 Activator PB125(®) as a Potential Therapeutic Agent against COVID-19 |
title_fullStr | Nrf2 Activator PB125(®) as a Potential Therapeutic Agent against COVID-19 |
title_full_unstemmed | Nrf2 Activator PB125(®) as a Potential Therapeutic Agent against COVID-19 |
title_short | Nrf2 Activator PB125(®) as a Potential Therapeutic Agent against COVID-19 |
title_sort | nrf2 activator pb125(®) as a potential therapeutic agent against covid-19 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7346195/ https://www.ncbi.nlm.nih.gov/pubmed/32545518 http://dx.doi.org/10.3390/antiox9060518 |
work_keys_str_mv | AT mccordjoem nrf2activatorpb125asapotentialtherapeuticagentagainstcovid19 AT hybertsonbrooksm nrf2activatorpb125asapotentialtherapeuticagentagainstcovid19 AT cotagomezadela nrf2activatorpb125asapotentialtherapeuticagentagainstcovid19 AT geracikarap nrf2activatorpb125asapotentialtherapeuticagentagainstcovid19 AT gaobifeng nrf2activatorpb125asapotentialtherapeuticagentagainstcovid19 |