The effects of glycyrrhizic acid and glabridin in the regulation of CXCL5 inflammation gene on acceleration of wound healing
Objective: To evaluate the anti-inflammatory property of both glycyrrhizic acid (GA) and glabridin in reducing inflammation to accelerate wound regeneration on 3T3-L1 and NIH-3T3 fibroblast cell lines. Methods: Cell proliferation and viability assay (MTT assay), scratch wound healing assays, and qua...
Published in: | Asian Pacific Journal of Tropical Biomedicine |
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Wolters Kluwer Medknow Publications
2016
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ftdoajarticles:oai:doaj.org/article:3e980ecd59fb4412a69886f8a50254f6 2023-05-15T15:07:19+02:00 The effects of glycyrrhizic acid and glabridin in the regulation of CXCL5 inflammation gene on acceleration of wound healing Hong Yung Yip Melissa Su Wei Poh Yoke Yin Chia 2016-02-01T00:00:00Z https://doi.org/10.1016/j.apjtb.2015.10.009 https://doaj.org/article/3e980ecd59fb4412a69886f8a50254f6 EN eng Wolters Kluwer Medknow Publications http://www.sciencedirect.com/science/article/pii/S2221169115002592 https://doaj.org/toc/2221-1691 2221-1691 doi:10.1016/j.apjtb.2015.10.009 https://doaj.org/article/3e980ecd59fb4412a69886f8a50254f6 Asian Pacific Journal of Tropical Biomedicine, Vol 6, Iss 2, Pp 108-113 (2016) Wound healing Glycyrrhizic acid Glabridin CXCL5 Inflammation Cell proliferation Cell migration Arctic medicine. Tropical medicine RC955-962 Biology (General) QH301-705.5 article 2016 ftdoajarticles https://doi.org/10.1016/j.apjtb.2015.10.009 2022-12-30T23:39:57Z Objective: To evaluate the anti-inflammatory property of both glycyrrhizic acid (GA) and glabridin in reducing inflammation to accelerate wound regeneration on 3T3-L1 and NIH-3T3 fibroblast cell lines. Methods: Cell proliferation and viability assay (MTT assay), scratch wound healing assays, and quantitative real-time PCR were conducted to investigate the effects on cell proliferation, cell migration, and expression of CXC chemokine ligand 5 inflammation gene respectively. Results: Results showed that at a low concentration of 1 × 10−8 mol/L, glabridin down regulated cell proliferation in NIH-3T3 significantly, suggesting its involvement in ERK1/2 signaling pathway. GA and glabridin significantly accelerated cell migration through wound healing in both 3T3-L1 and NIH-3T3 and significantly down regulated the expression of CXC chemokine ligand 5 in 3T3-L1 at concentration 1 × 10−8 mol/L, indicating the possible involvement of nuclear factor-κB and cyclooxygenase 2 transcriptions modulation. Conclusions: Both GA and glabridin can serve as potential treatment for chronic inflammatory disease, and glabridin as an oncogenic inhibitor due to its anti-proliferative property. Article in Journal/Newspaper Arctic Directory of Open Access Journals: DOAJ Articles Arctic Asian Pacific Journal of Tropical Biomedicine 6 2 108 113 |
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Open Polar |
collection |
Directory of Open Access Journals: DOAJ Articles |
op_collection_id |
ftdoajarticles |
language |
English |
topic |
Wound healing Glycyrrhizic acid Glabridin CXCL5 Inflammation Cell proliferation Cell migration Arctic medicine. Tropical medicine RC955-962 Biology (General) QH301-705.5 |
spellingShingle |
Wound healing Glycyrrhizic acid Glabridin CXCL5 Inflammation Cell proliferation Cell migration Arctic medicine. Tropical medicine RC955-962 Biology (General) QH301-705.5 Hong Yung Yip Melissa Su Wei Poh Yoke Yin Chia The effects of glycyrrhizic acid and glabridin in the regulation of CXCL5 inflammation gene on acceleration of wound healing |
topic_facet |
Wound healing Glycyrrhizic acid Glabridin CXCL5 Inflammation Cell proliferation Cell migration Arctic medicine. Tropical medicine RC955-962 Biology (General) QH301-705.5 |
description |
Objective: To evaluate the anti-inflammatory property of both glycyrrhizic acid (GA) and glabridin in reducing inflammation to accelerate wound regeneration on 3T3-L1 and NIH-3T3 fibroblast cell lines. Methods: Cell proliferation and viability assay (MTT assay), scratch wound healing assays, and quantitative real-time PCR were conducted to investigate the effects on cell proliferation, cell migration, and expression of CXC chemokine ligand 5 inflammation gene respectively. Results: Results showed that at a low concentration of 1 × 10−8 mol/L, glabridin down regulated cell proliferation in NIH-3T3 significantly, suggesting its involvement in ERK1/2 signaling pathway. GA and glabridin significantly accelerated cell migration through wound healing in both 3T3-L1 and NIH-3T3 and significantly down regulated the expression of CXC chemokine ligand 5 in 3T3-L1 at concentration 1 × 10−8 mol/L, indicating the possible involvement of nuclear factor-κB and cyclooxygenase 2 transcriptions modulation. Conclusions: Both GA and glabridin can serve as potential treatment for chronic inflammatory disease, and glabridin as an oncogenic inhibitor due to its anti-proliferative property. |
format |
Article in Journal/Newspaper |
author |
Hong Yung Yip Melissa Su Wei Poh Yoke Yin Chia |
author_facet |
Hong Yung Yip Melissa Su Wei Poh Yoke Yin Chia |
author_sort |
Hong Yung Yip |
title |
The effects of glycyrrhizic acid and glabridin in the regulation of CXCL5 inflammation gene on acceleration of wound healing |
title_short |
The effects of glycyrrhizic acid and glabridin in the regulation of CXCL5 inflammation gene on acceleration of wound healing |
title_full |
The effects of glycyrrhizic acid and glabridin in the regulation of CXCL5 inflammation gene on acceleration of wound healing |
title_fullStr |
The effects of glycyrrhizic acid and glabridin in the regulation of CXCL5 inflammation gene on acceleration of wound healing |
title_full_unstemmed |
The effects of glycyrrhizic acid and glabridin in the regulation of CXCL5 inflammation gene on acceleration of wound healing |
title_sort |
effects of glycyrrhizic acid and glabridin in the regulation of cxcl5 inflammation gene on acceleration of wound healing |
publisher |
Wolters Kluwer Medknow Publications |
publishDate |
2016 |
url |
https://doi.org/10.1016/j.apjtb.2015.10.009 https://doaj.org/article/3e980ecd59fb4412a69886f8a50254f6 |
geographic |
Arctic |
geographic_facet |
Arctic |
genre |
Arctic |
genre_facet |
Arctic |
op_source |
Asian Pacific Journal of Tropical Biomedicine, Vol 6, Iss 2, Pp 108-113 (2016) |
op_relation |
http://www.sciencedirect.com/science/article/pii/S2221169115002592 https://doaj.org/toc/2221-1691 2221-1691 doi:10.1016/j.apjtb.2015.10.009 https://doaj.org/article/3e980ecd59fb4412a69886f8a50254f6 |
op_doi |
https://doi.org/10.1016/j.apjtb.2015.10.009 |
container_title |
Asian Pacific Journal of Tropical Biomedicine |
container_volume |
6 |
container_issue |
2 |
container_start_page |
108 |
op_container_end_page |
113 |
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1766338842907901952 |