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In Vivo Early Intervention and the Therapeutic Effects of 20(S)-Ginsenoside Rg3 on Hypertrophic Scar Formation

BACKGROUND: Intra-lesional injections of corticosteroids, interferon, and chemotherapeutic drugs are currently the most popular treatments of hypertrophic scar formation. However, these drugs can only be used after HS is formed, and not during the inflammatory phase of wound healing, which regulates...

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Autores principales: Cheng, Liying, Sun, Xiaoming, Hu, Changmin, Jin, Rong, Sun, Baoshan, Shi, Yaoming, Cui, Wenguo, Zhang, Yuguang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4264739/
https://www.ncbi.nlm.nih.gov/pubmed/25502572
http://dx.doi.org/10.1371/journal.pone.0113640
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author Cheng, Liying
Sun, Xiaoming
Hu, Changmin
Jin, Rong
Sun, Baoshan
Shi, Yaoming
Cui, Wenguo
Zhang, Yuguang
author_facet Cheng, Liying
Sun, Xiaoming
Hu, Changmin
Jin, Rong
Sun, Baoshan
Shi, Yaoming
Cui, Wenguo
Zhang, Yuguang
author_sort Cheng, Liying
collection PubMed
description BACKGROUND: Intra-lesional injections of corticosteroids, interferon, and chemotherapeutic drugs are currently the most popular treatments of hypertrophic scar formation. However, these drugs can only be used after HS is formed, and not during the inflammatory phase of wound healing, which regulates the HS forming process. OBJECTIVE: To investigate a new, effective, combining therapeutic and safe drug for early intervention and treatment for hypertrophic scars. METHODS: Cell viability assay and flow cytometric analysis were studied in vitro. Animal studies were done to investigate the combining therapeutic effects of 20(S)-ginsenoside Rg3 (Rg3) on the inflammatory phase of wound healing and HS formation. RESULTS: In vitro studies showed that Rg3 can inhibit HS fibroblasts proliferation and induce HSF apoptosis in a concentration-dependent manner. In vivo studies demonstrated that Rg3 can limit the exaggerated inflammation, and do not delay the wound healing process, which indicates that Rg3 could be used as an early intervention to reduce HS formation. Topical injection of 4 mg/mL Rg3 can reduce HS formation by 34%. Histological and molecular studies revealed that Rg3 injection inhibits fibroblasts proliferation thus reduced the accumulation of collagen fibers, and down-regulates VEGF expression in the HS tissue. CONCLUSION: Rg3 can be employed as an early intervention and a combining therapeutic drug to reduce inflammation and HS formation as well.
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spelling pubmed-42647392014-12-19 In Vivo Early Intervention and the Therapeutic Effects of 20(S)-Ginsenoside Rg3 on Hypertrophic Scar Formation Cheng, Liying Sun, Xiaoming Hu, Changmin Jin, Rong Sun, Baoshan Shi, Yaoming Cui, Wenguo Zhang, Yuguang PLoS One Research Article BACKGROUND: Intra-lesional injections of corticosteroids, interferon, and chemotherapeutic drugs are currently the most popular treatments of hypertrophic scar formation. However, these drugs can only be used after HS is formed, and not during the inflammatory phase of wound healing, which regulates the HS forming process. OBJECTIVE: To investigate a new, effective, combining therapeutic and safe drug for early intervention and treatment for hypertrophic scars. METHODS: Cell viability assay and flow cytometric analysis were studied in vitro. Animal studies were done to investigate the combining therapeutic effects of 20(S)-ginsenoside Rg3 (Rg3) on the inflammatory phase of wound healing and HS formation. RESULTS: In vitro studies showed that Rg3 can inhibit HS fibroblasts proliferation and induce HSF apoptosis in a concentration-dependent manner. In vivo studies demonstrated that Rg3 can limit the exaggerated inflammation, and do not delay the wound healing process, which indicates that Rg3 could be used as an early intervention to reduce HS formation. Topical injection of 4 mg/mL Rg3 can reduce HS formation by 34%. Histological and molecular studies revealed that Rg3 injection inhibits fibroblasts proliferation thus reduced the accumulation of collagen fibers, and down-regulates VEGF expression in the HS tissue. CONCLUSION: Rg3 can be employed as an early intervention and a combining therapeutic drug to reduce inflammation and HS formation as well. Public Library of Science 2014-12-12 /pmc/articles/PMC4264739/ /pubmed/25502572 http://dx.doi.org/10.1371/journal.pone.0113640 Text en © 2014 Cheng et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Cheng, Liying
Sun, Xiaoming
Hu, Changmin
Jin, Rong
Sun, Baoshan
Shi, Yaoming
Cui, Wenguo
Zhang, Yuguang
In Vivo Early Intervention and the Therapeutic Effects of 20(S)-Ginsenoside Rg3 on Hypertrophic Scar Formation
title In Vivo Early Intervention and the Therapeutic Effects of 20(S)-Ginsenoside Rg3 on Hypertrophic Scar Formation
title_full In Vivo Early Intervention and the Therapeutic Effects of 20(S)-Ginsenoside Rg3 on Hypertrophic Scar Formation
title_fullStr In Vivo Early Intervention and the Therapeutic Effects of 20(S)-Ginsenoside Rg3 on Hypertrophic Scar Formation
title_full_unstemmed In Vivo Early Intervention and the Therapeutic Effects of 20(S)-Ginsenoside Rg3 on Hypertrophic Scar Formation
title_short In Vivo Early Intervention and the Therapeutic Effects of 20(S)-Ginsenoside Rg3 on Hypertrophic Scar Formation
title_sort in vivo early intervention and the therapeutic effects of 20(s)-ginsenoside rg3 on hypertrophic scar formation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4264739/
https://www.ncbi.nlm.nih.gov/pubmed/25502572
http://dx.doi.org/10.1371/journal.pone.0113640
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