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Gintonin, an exogenous ginseng-derived LPA receptor ligand, promotes corneal wound healing
Ginseng gintonin is an exogenous ligand of lysophosphatidic acid (LPA) receptors. Accumulating evidence shows LPA helps in rapid recovery of corneal damage. The aim of this study was to evaluate the therapeutic efficacy of gintonin in a rabbit model of corneal damage. We investigated the signal tran...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society of Veterinary Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5639092/ https://www.ncbi.nlm.nih.gov/pubmed/27586470 http://dx.doi.org/10.4142/jvs.2017.18.3.387 |
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author | Kim, Hyeon-Joong Kim, Joon Young Lee, Byung-Hwan Choi, Sun-Hye Rhim, Hyewon Kim, Hyoung-Chun Ahn, Seoung-Yob Jeong, Soon-Wuk Jang, Minhee Cho, Ik-Hyun Nah, Seung-Yeol |
author_facet | Kim, Hyeon-Joong Kim, Joon Young Lee, Byung-Hwan Choi, Sun-Hye Rhim, Hyewon Kim, Hyoung-Chun Ahn, Seoung-Yob Jeong, Soon-Wuk Jang, Minhee Cho, Ik-Hyun Nah, Seung-Yeol |
author_sort | Kim, Hyeon-Joong |
collection | PubMed |
description | Ginseng gintonin is an exogenous ligand of lysophosphatidic acid (LPA) receptors. Accumulating evidence shows LPA helps in rapid recovery of corneal damage. The aim of this study was to evaluate the therapeutic efficacy of gintonin in a rabbit model of corneal damage. We investigated the signal transduction pathway of gintonin in human corneal epithelium (HCE) cells to elucidate the underlying molecular mechanism. We next evaluated the therapeutic effects of gintonin, using a rabbit model of corneal damage, by undertaking histochemical analysis. Treatment of gintonin to HCE cells induced transient increases of [Ca(2+)](i) in concentration-dependent and reversible manners. Gintonin-mediated mobilization of [Ca(2+)](i) was attenuated by LPA1/3 receptor antagonist Ki16425, phospholipase C inhibitor U73122, inositol 1,4,5-triphosphate receptor antagonist 2-APB, and intracellular Ca(2+) chelator BAPTA-AM. Gintonin facilitated in vitro wound healing in a concentration-dependent manner. When applied as an eye-drop to rabbits with corneal damage, gintonin rapidly promoted recovery. Histochemical analysis showed gintonin decreased corneal apoptosis and increased corneal cell proliferation. We demonstrated that LPA receptor activation by gintonin is linked to in vitro and in vivo therapeutic effects against corneal damage. Gintonin can be applied as a clinical agent for the rapid healing of corneal damage. |
format | Online Article Text |
id | pubmed-5639092 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The Korean Society of Veterinary Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-56390922017-10-17 Gintonin, an exogenous ginseng-derived LPA receptor ligand, promotes corneal wound healing Kim, Hyeon-Joong Kim, Joon Young Lee, Byung-Hwan Choi, Sun-Hye Rhim, Hyewon Kim, Hyoung-Chun Ahn, Seoung-Yob Jeong, Soon-Wuk Jang, Minhee Cho, Ik-Hyun Nah, Seung-Yeol J Vet Sci Original Article Ginseng gintonin is an exogenous ligand of lysophosphatidic acid (LPA) receptors. Accumulating evidence shows LPA helps in rapid recovery of corneal damage. The aim of this study was to evaluate the therapeutic efficacy of gintonin in a rabbit model of corneal damage. We investigated the signal transduction pathway of gintonin in human corneal epithelium (HCE) cells to elucidate the underlying molecular mechanism. We next evaluated the therapeutic effects of gintonin, using a rabbit model of corneal damage, by undertaking histochemical analysis. Treatment of gintonin to HCE cells induced transient increases of [Ca(2+)](i) in concentration-dependent and reversible manners. Gintonin-mediated mobilization of [Ca(2+)](i) was attenuated by LPA1/3 receptor antagonist Ki16425, phospholipase C inhibitor U73122, inositol 1,4,5-triphosphate receptor antagonist 2-APB, and intracellular Ca(2+) chelator BAPTA-AM. Gintonin facilitated in vitro wound healing in a concentration-dependent manner. When applied as an eye-drop to rabbits with corneal damage, gintonin rapidly promoted recovery. Histochemical analysis showed gintonin decreased corneal apoptosis and increased corneal cell proliferation. We demonstrated that LPA receptor activation by gintonin is linked to in vitro and in vivo therapeutic effects against corneal damage. Gintonin can be applied as a clinical agent for the rapid healing of corneal damage. The Korean Society of Veterinary Science 2017-09 2017-09-20 /pmc/articles/PMC5639092/ /pubmed/27586470 http://dx.doi.org/10.4142/jvs.2017.18.3.387 Text en © 2017 The Korean Society of Veterinary Science http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Kim, Hyeon-Joong Kim, Joon Young Lee, Byung-Hwan Choi, Sun-Hye Rhim, Hyewon Kim, Hyoung-Chun Ahn, Seoung-Yob Jeong, Soon-Wuk Jang, Minhee Cho, Ik-Hyun Nah, Seung-Yeol Gintonin, an exogenous ginseng-derived LPA receptor ligand, promotes corneal wound healing |
title | Gintonin, an exogenous ginseng-derived LPA receptor ligand, promotes corneal wound healing |
title_full | Gintonin, an exogenous ginseng-derived LPA receptor ligand, promotes corneal wound healing |
title_fullStr | Gintonin, an exogenous ginseng-derived LPA receptor ligand, promotes corneal wound healing |
title_full_unstemmed | Gintonin, an exogenous ginseng-derived LPA receptor ligand, promotes corneal wound healing |
title_short | Gintonin, an exogenous ginseng-derived LPA receptor ligand, promotes corneal wound healing |
title_sort | gintonin, an exogenous ginseng-derived lpa receptor ligand, promotes corneal wound healing |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5639092/ https://www.ncbi.nlm.nih.gov/pubmed/27586470 http://dx.doi.org/10.4142/jvs.2017.18.3.387 |
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