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Effects of fermented black ginseng on wound healing mediated by angiogenesis through the mitogen-activated protein kinase pathway in human umbilical vein endothelial cells
BACKGROUND: Fermented black ginseng (FBG) is produced through several cycles of steam treatment of raw ginseng, at which point its color turns black. During this process, the original ginsenoside components of raw ginseng (e.g., Re, Rg1, Rb1, Rc, and Rb2) are altered, and less-polar ginsenosides are...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6190532/ https://www.ncbi.nlm.nih.gov/pubmed/30337813 http://dx.doi.org/10.1016/j.jgr.2017.07.006 |
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author | Park, Jun Yeon Lee, Dong-Soo Kim, Chang-Eop Shin, Myoung-Sook Seo, Chang-Seob Shin, Hyeun-Kyoo Hwang, Gwi Seo An, Jun Min Kim, Su-Nam Kang, Ki Sung |
author_facet | Park, Jun Yeon Lee, Dong-Soo Kim, Chang-Eop Shin, Myoung-Sook Seo, Chang-Seob Shin, Hyeun-Kyoo Hwang, Gwi Seo An, Jun Min Kim, Su-Nam Kang, Ki Sung |
author_sort | Park, Jun Yeon |
collection | PubMed |
description | BACKGROUND: Fermented black ginseng (FBG) is produced through several cycles of steam treatment of raw ginseng, at which point its color turns black. During this process, the original ginsenoside components of raw ginseng (e.g., Re, Rg1, Rb1, Rc, and Rb2) are altered, and less-polar ginsenosides are generated (e.g., Rg3, Rg5, Rk1, and Rh4). The aim of this study was to determine the effect of FBG on wound healing. METHODS: The effects of FBG on tube formation and on scratch wound healing were measured using human umbilical vein endothelial cells (HUVECs) and HaCaT cells, respectively. Protein phosphorylation of mitogen-activated protein kinase was evaluated via Western blotting. Finally, the wound-healing effects of FBG were assessed using an experimental cutaneous wounds model in mice. RESULTS AND CONCLUSION: The results showed that FBG enhanced the tube formation in HUVECs and migration in HaCaT cells. Western blot analysis revealed that FBG stimulated the phosphorylation of p38 and extracellular signal-regulated kinase in HaCaT cells. Moreover, mice treated with 25 μg/mL of FBG exhibited faster wound closure than the control mice did in the experimental cutaneous wounds model in mice. |
format | Online Article Text |
id | pubmed-6190532 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-61905322018-10-18 Effects of fermented black ginseng on wound healing mediated by angiogenesis through the mitogen-activated protein kinase pathway in human umbilical vein endothelial cells Park, Jun Yeon Lee, Dong-Soo Kim, Chang-Eop Shin, Myoung-Sook Seo, Chang-Seob Shin, Hyeun-Kyoo Hwang, Gwi Seo An, Jun Min Kim, Su-Nam Kang, Ki Sung J Ginseng Res Research Article BACKGROUND: Fermented black ginseng (FBG) is produced through several cycles of steam treatment of raw ginseng, at which point its color turns black. During this process, the original ginsenoside components of raw ginseng (e.g., Re, Rg1, Rb1, Rc, and Rb2) are altered, and less-polar ginsenosides are generated (e.g., Rg3, Rg5, Rk1, and Rh4). The aim of this study was to determine the effect of FBG on wound healing. METHODS: The effects of FBG on tube formation and on scratch wound healing were measured using human umbilical vein endothelial cells (HUVECs) and HaCaT cells, respectively. Protein phosphorylation of mitogen-activated protein kinase was evaluated via Western blotting. Finally, the wound-healing effects of FBG were assessed using an experimental cutaneous wounds model in mice. RESULTS AND CONCLUSION: The results showed that FBG enhanced the tube formation in HUVECs and migration in HaCaT cells. Western blot analysis revealed that FBG stimulated the phosphorylation of p38 and extracellular signal-regulated kinase in HaCaT cells. Moreover, mice treated with 25 μg/mL of FBG exhibited faster wound closure than the control mice did in the experimental cutaneous wounds model in mice. Elsevier 2018-10 2017-07-25 /pmc/articles/PMC6190532/ /pubmed/30337813 http://dx.doi.org/10.1016/j.jgr.2017.07.006 Text en © 2017 The Korean Society of Ginseng, Published by Elsevier Korea LLC. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Article Park, Jun Yeon Lee, Dong-Soo Kim, Chang-Eop Shin, Myoung-Sook Seo, Chang-Seob Shin, Hyeun-Kyoo Hwang, Gwi Seo An, Jun Min Kim, Su-Nam Kang, Ki Sung Effects of fermented black ginseng on wound healing mediated by angiogenesis through the mitogen-activated protein kinase pathway in human umbilical vein endothelial cells |
title | Effects of fermented black ginseng on wound healing mediated by angiogenesis through the mitogen-activated protein kinase pathway in human umbilical vein endothelial cells |
title_full | Effects of fermented black ginseng on wound healing mediated by angiogenesis through the mitogen-activated protein kinase pathway in human umbilical vein endothelial cells |
title_fullStr | Effects of fermented black ginseng on wound healing mediated by angiogenesis through the mitogen-activated protein kinase pathway in human umbilical vein endothelial cells |
title_full_unstemmed | Effects of fermented black ginseng on wound healing mediated by angiogenesis through the mitogen-activated protein kinase pathway in human umbilical vein endothelial cells |
title_short | Effects of fermented black ginseng on wound healing mediated by angiogenesis through the mitogen-activated protein kinase pathway in human umbilical vein endothelial cells |
title_sort | effects of fermented black ginseng on wound healing mediated by angiogenesis through the mitogen-activated protein kinase pathway in human umbilical vein endothelial cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6190532/ https://www.ncbi.nlm.nih.gov/pubmed/30337813 http://dx.doi.org/10.1016/j.jgr.2017.07.006 |
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