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Inhibition of hypertrophic scar formation with oral asiaticoside treatment in a rabbit ear scar model
Hypertrophic scar (HS) is a fibrotic skin disease characterised by over‐productive collagen and excessive inflammatory reaction, which can be functionally and cosmetically problematic. A scar‐prone constitute will accelerate HS formation and functional disorder, which deserves systemic therapy with...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8450800/ https://www.ncbi.nlm.nih.gov/pubmed/33666348 http://dx.doi.org/10.1111/iwj.13561 |
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author | Huang, Jia Zhou, Xiaobo Xia, Lingling Liu, Weiwei Guo, Fei Liu, Jianhui Liu, Wei |
author_facet | Huang, Jia Zhou, Xiaobo Xia, Lingling Liu, Weiwei Guo, Fei Liu, Jianhui Liu, Wei |
author_sort | Huang, Jia |
collection | PubMed |
description | Hypertrophic scar (HS) is a fibrotic skin disease characterised by over‐productive collagen and excessive inflammatory reaction, which can be functionally and cosmetically problematic. A scar‐prone constitute will accelerate HS formation and functional disorder, which deserves systemic therapy with oral medicine. To examine the oral therapeutic effectiveness on HS with convincing evidence of gross view and histological improvement, a rabbit ear HS model was employed with oral administration of asiaticoside (AS) at the doses of 12 and 24 mg kg(−1) d(−1) daily for 60 consecutive days. Gross observation and histological findings showed that oral AS treatment could significantly inhibit HS formation in a dose dependent manner. Semi‐quantification of scar elevation index at days 7, 15, 30, and 60, and quantitative polymerase chain reaction at days 30 and 60 also provided the evidences of reduced scar thickness and inhibited fibrotic gene expressions of collagens I, III, TGF‐β1, interleukins 1β, 6 and 8, and enhanced gene expression of SMAD 7 and PPAR‐γ with a dose‐dependent manner. These results indicated that AS is likely to serve as a systemic therapeutic agent of HS treatment for those who may have scar‐prone constitute via anti‐inflammation, inhibiting fibrotic process, and enhancing matrix degradation. |
format | Online Article Text |
id | pubmed-8450800 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-84508002021-09-27 Inhibition of hypertrophic scar formation with oral asiaticoside treatment in a rabbit ear scar model Huang, Jia Zhou, Xiaobo Xia, Lingling Liu, Weiwei Guo, Fei Liu, Jianhui Liu, Wei Int Wound J Original Articles Hypertrophic scar (HS) is a fibrotic skin disease characterised by over‐productive collagen and excessive inflammatory reaction, which can be functionally and cosmetically problematic. A scar‐prone constitute will accelerate HS formation and functional disorder, which deserves systemic therapy with oral medicine. To examine the oral therapeutic effectiveness on HS with convincing evidence of gross view and histological improvement, a rabbit ear HS model was employed with oral administration of asiaticoside (AS) at the doses of 12 and 24 mg kg(−1) d(−1) daily for 60 consecutive days. Gross observation and histological findings showed that oral AS treatment could significantly inhibit HS formation in a dose dependent manner. Semi‐quantification of scar elevation index at days 7, 15, 30, and 60, and quantitative polymerase chain reaction at days 30 and 60 also provided the evidences of reduced scar thickness and inhibited fibrotic gene expressions of collagens I, III, TGF‐β1, interleukins 1β, 6 and 8, and enhanced gene expression of SMAD 7 and PPAR‐γ with a dose‐dependent manner. These results indicated that AS is likely to serve as a systemic therapeutic agent of HS treatment for those who may have scar‐prone constitute via anti‐inflammation, inhibiting fibrotic process, and enhancing matrix degradation. Blackwell Publishing Ltd 2021-03-05 /pmc/articles/PMC8450800/ /pubmed/33666348 http://dx.doi.org/10.1111/iwj.13561 Text en © 2021 The Authors. International Wound Journal published by Medicalhelplines.com Inc (3M) and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Huang, Jia Zhou, Xiaobo Xia, Lingling Liu, Weiwei Guo, Fei Liu, Jianhui Liu, Wei Inhibition of hypertrophic scar formation with oral asiaticoside treatment in a rabbit ear scar model |
title | Inhibition of hypertrophic scar formation with oral asiaticoside treatment in a rabbit ear scar model |
title_full | Inhibition of hypertrophic scar formation with oral asiaticoside treatment in a rabbit ear scar model |
title_fullStr | Inhibition of hypertrophic scar formation with oral asiaticoside treatment in a rabbit ear scar model |
title_full_unstemmed | Inhibition of hypertrophic scar formation with oral asiaticoside treatment in a rabbit ear scar model |
title_short | Inhibition of hypertrophic scar formation with oral asiaticoside treatment in a rabbit ear scar model |
title_sort | inhibition of hypertrophic scar formation with oral asiaticoside treatment in a rabbit ear scar model |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8450800/ https://www.ncbi.nlm.nih.gov/pubmed/33666348 http://dx.doi.org/10.1111/iwj.13561 |
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