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Cytoprotective effects of Avenathramide C against oxidative and inflammatory stress in normal human dermal fibroblasts
Natural polyphenols are promising anti-aging compounds not only for their antioxidant activity, but also their ability to activate specific cellular pathways mediating the aging process. Avenanthramide C (Avn C), found exclusively in oats, is a natural antioxidant associated with free radical scaven...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6393498/ https://www.ncbi.nlm.nih.gov/pubmed/30814621 http://dx.doi.org/10.1038/s41598-019-39244-9 |
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author | Wang, Chenxuan Eskiw, Christopher H. |
author_facet | Wang, Chenxuan Eskiw, Christopher H. |
author_sort | Wang, Chenxuan |
collection | PubMed |
description | Natural polyphenols are promising anti-aging compounds not only for their antioxidant activity, but also their ability to activate specific cellular pathways mediating the aging process. Avenanthramide C (Avn C), found exclusively in oats, is a natural antioxidant associated with free radical scavenging; however, it is how this compound elicits other protective effects. We investigated the intracellular antioxidant activity of Avn C and other cytoprotective potential in normal human skin fibroblasts exposed to extracellular stress. Avn C reduced H(2)O(2)-induced oxidative stress by reducing intracellular free radical levels and antioxidant gene transcripts. Avn C also resulted in decreased levels of gene transcripts encoding pro-inflammatory cytokines in response to H(2)O(2) or tumor necrosis factor-α (TNF-α). This reduction in cytokine gene transcription occurred concomitantly with reduced phosphorylated nuclear factor-κB (NF-κB) p65, and decreased NF-κB DNA binding. Avn C further induced heme oxygense-1 (HO-1) expression through increased Nrf2 DNA binding activity, demonstrating a second mechanism by which Avn C attenuates cellular stress. Collectively, our findings indicate that Avn C protects normal human skin fibroblasts against oxidative stress and inflammatory response through NF-κB inhibition and Nrf2/HO-1 activation. |
format | Online Article Text |
id | pubmed-6393498 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63934982019-03-01 Cytoprotective effects of Avenathramide C against oxidative and inflammatory stress in normal human dermal fibroblasts Wang, Chenxuan Eskiw, Christopher H. Sci Rep Article Natural polyphenols are promising anti-aging compounds not only for their antioxidant activity, but also their ability to activate specific cellular pathways mediating the aging process. Avenanthramide C (Avn C), found exclusively in oats, is a natural antioxidant associated with free radical scavenging; however, it is how this compound elicits other protective effects. We investigated the intracellular antioxidant activity of Avn C and other cytoprotective potential in normal human skin fibroblasts exposed to extracellular stress. Avn C reduced H(2)O(2)-induced oxidative stress by reducing intracellular free radical levels and antioxidant gene transcripts. Avn C also resulted in decreased levels of gene transcripts encoding pro-inflammatory cytokines in response to H(2)O(2) or tumor necrosis factor-α (TNF-α). This reduction in cytokine gene transcription occurred concomitantly with reduced phosphorylated nuclear factor-κB (NF-κB) p65, and decreased NF-κB DNA binding. Avn C further induced heme oxygense-1 (HO-1) expression through increased Nrf2 DNA binding activity, demonstrating a second mechanism by which Avn C attenuates cellular stress. Collectively, our findings indicate that Avn C protects normal human skin fibroblasts against oxidative stress and inflammatory response through NF-κB inhibition and Nrf2/HO-1 activation. Nature Publishing Group UK 2019-02-27 /pmc/articles/PMC6393498/ /pubmed/30814621 http://dx.doi.org/10.1038/s41598-019-39244-9 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Wang, Chenxuan Eskiw, Christopher H. Cytoprotective effects of Avenathramide C against oxidative and inflammatory stress in normal human dermal fibroblasts |
title | Cytoprotective effects of Avenathramide C against oxidative and inflammatory stress in normal human dermal fibroblasts |
title_full | Cytoprotective effects of Avenathramide C against oxidative and inflammatory stress in normal human dermal fibroblasts |
title_fullStr | Cytoprotective effects of Avenathramide C against oxidative and inflammatory stress in normal human dermal fibroblasts |
title_full_unstemmed | Cytoprotective effects of Avenathramide C against oxidative and inflammatory stress in normal human dermal fibroblasts |
title_short | Cytoprotective effects of Avenathramide C against oxidative and inflammatory stress in normal human dermal fibroblasts |
title_sort | cytoprotective effects of avenathramide c against oxidative and inflammatory stress in normal human dermal fibroblasts |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6393498/ https://www.ncbi.nlm.nih.gov/pubmed/30814621 http://dx.doi.org/10.1038/s41598-019-39244-9 |
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