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Echinochrome A Protects against Ultraviolet B-induced Photoaging by Lowering Collagen Degradation and Inflammatory Cell Infiltration in Hairless Mice
Echinochrome A (Ech A, 7-ethyl-2,3,5,6,8-pentahydroxy-1,4-naphthoquinone) has been known to exhibit anti-oxidative and anti-inflammatory effects. However, no study has been carried out on the efficacy of Ech A against skin photoaging; this process is largely mediated by oxidative stress. Six-week-ol...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8537837/ https://www.ncbi.nlm.nih.gov/pubmed/34677449 http://dx.doi.org/10.3390/md19100550 |
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author | Seol, Jung Eun Ahn, Sang Woo Seol, Bomin Yun, Hyeong Rok Park, Nammi Kim, Hyoung Kyu Vasileva, Elena A. Mishchenko, Natalia P. Fedoreyev, Sergey A. Stonik, Valentin A. Han, Jin |
author_facet | Seol, Jung Eun Ahn, Sang Woo Seol, Bomin Yun, Hyeong Rok Park, Nammi Kim, Hyoung Kyu Vasileva, Elena A. Mishchenko, Natalia P. Fedoreyev, Sergey A. Stonik, Valentin A. Han, Jin |
author_sort | Seol, Jung Eun |
collection | PubMed |
description | Echinochrome A (Ech A, 7-ethyl-2,3,5,6,8-pentahydroxy-1,4-naphthoquinone) has been known to exhibit anti-oxidative and anti-inflammatory effects. However, no study has been carried out on the efficacy of Ech A against skin photoaging; this process is largely mediated by oxidative stress. Six-week-old male SKH-1 hairless mice (n = 36) were divided into five groups. Except for a group that were not treated (n = 4), all mice underwent ultraviolet-B (UVB) exposure for 8 weeks while applying phosphate-buffered saline or Ech A through intraperitoneal injection. UVB impaired skin barrier function, showing increased transepidermal water loss and decreased stratum corneum hydration. UVB induced dermal collagen degeneration and mast cell infiltration. Ech A injection was found to significantly lower transepidermal water loss while attenuating tissue inflammatory changes and collagen degeneration compared to the control. Furthermore, Ech A was found to decrease the relative expression of matrix metalloproteinase, tryptase, and chymase. Taken together, these results suggest that Ech A protects against UVB-induced photoaging in both functional and histologic aspects, causing a lowering of collagen degradation and inflammatory cell infiltration. |
format | Online Article Text |
id | pubmed-8537837 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-85378372021-10-24 Echinochrome A Protects against Ultraviolet B-induced Photoaging by Lowering Collagen Degradation and Inflammatory Cell Infiltration in Hairless Mice Seol, Jung Eun Ahn, Sang Woo Seol, Bomin Yun, Hyeong Rok Park, Nammi Kim, Hyoung Kyu Vasileva, Elena A. Mishchenko, Natalia P. Fedoreyev, Sergey A. Stonik, Valentin A. Han, Jin Mar Drugs Article Echinochrome A (Ech A, 7-ethyl-2,3,5,6,8-pentahydroxy-1,4-naphthoquinone) has been known to exhibit anti-oxidative and anti-inflammatory effects. However, no study has been carried out on the efficacy of Ech A against skin photoaging; this process is largely mediated by oxidative stress. Six-week-old male SKH-1 hairless mice (n = 36) were divided into five groups. Except for a group that were not treated (n = 4), all mice underwent ultraviolet-B (UVB) exposure for 8 weeks while applying phosphate-buffered saline or Ech A through intraperitoneal injection. UVB impaired skin barrier function, showing increased transepidermal water loss and decreased stratum corneum hydration. UVB induced dermal collagen degeneration and mast cell infiltration. Ech A injection was found to significantly lower transepidermal water loss while attenuating tissue inflammatory changes and collagen degeneration compared to the control. Furthermore, Ech A was found to decrease the relative expression of matrix metalloproteinase, tryptase, and chymase. Taken together, these results suggest that Ech A protects against UVB-induced photoaging in both functional and histologic aspects, causing a lowering of collagen degradation and inflammatory cell infiltration. MDPI 2021-09-28 /pmc/articles/PMC8537837/ /pubmed/34677449 http://dx.doi.org/10.3390/md19100550 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Seol, Jung Eun Ahn, Sang Woo Seol, Bomin Yun, Hyeong Rok Park, Nammi Kim, Hyoung Kyu Vasileva, Elena A. Mishchenko, Natalia P. Fedoreyev, Sergey A. Stonik, Valentin A. Han, Jin Echinochrome A Protects against Ultraviolet B-induced Photoaging by Lowering Collagen Degradation and Inflammatory Cell Infiltration in Hairless Mice |
title | Echinochrome A Protects against Ultraviolet B-induced Photoaging by Lowering Collagen Degradation and Inflammatory Cell Infiltration in Hairless Mice |
title_full | Echinochrome A Protects against Ultraviolet B-induced Photoaging by Lowering Collagen Degradation and Inflammatory Cell Infiltration in Hairless Mice |
title_fullStr | Echinochrome A Protects against Ultraviolet B-induced Photoaging by Lowering Collagen Degradation and Inflammatory Cell Infiltration in Hairless Mice |
title_full_unstemmed | Echinochrome A Protects against Ultraviolet B-induced Photoaging by Lowering Collagen Degradation and Inflammatory Cell Infiltration in Hairless Mice |
title_short | Echinochrome A Protects against Ultraviolet B-induced Photoaging by Lowering Collagen Degradation and Inflammatory Cell Infiltration in Hairless Mice |
title_sort | echinochrome a protects against ultraviolet b-induced photoaging by lowering collagen degradation and inflammatory cell infiltration in hairless mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8537837/ https://www.ncbi.nlm.nih.gov/pubmed/34677449 http://dx.doi.org/10.3390/md19100550 |
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