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Ameliorative effect of black ginseng extract against oxidative stress-induced cellular damages in mouse hepatocytes

BACKGROUND: Oxidative stress induces the production of reactive oxygen species (ROS), which play important causative roles in various pathological conditions. Black ginseng (BG), a type of steam-processed ginseng, has drawn significant attention due to its biological activity, and is more potent tha...

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Autores principales: Choudhry, Qaisra Naheed, Kim, Jun Ho, Cho, Hyung Taek, Heo, Wan, Lee, Jeong-Jun, Lee, Jin Hyup, Kim, Young Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6437468/
https://www.ncbi.nlm.nih.gov/pubmed/30976158
http://dx.doi.org/10.1016/j.jgr.2017.10.003
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author Choudhry, Qaisra Naheed
Kim, Jun Ho
Cho, Hyung Taek
Heo, Wan
Lee, Jeong-Jun
Lee, Jin Hyup
Kim, Young Jun
author_facet Choudhry, Qaisra Naheed
Kim, Jun Ho
Cho, Hyung Taek
Heo, Wan
Lee, Jeong-Jun
Lee, Jin Hyup
Kim, Young Jun
author_sort Choudhry, Qaisra Naheed
collection PubMed
description BACKGROUND: Oxidative stress induces the production of reactive oxygen species (ROS), which play important causative roles in various pathological conditions. Black ginseng (BG), a type of steam-processed ginseng, has drawn significant attention due to its biological activity, and is more potent than white ginseng (WG) or red ginseng (RG). METHODS: We evaluated the protective effects of BG extract (BGE) against oxidative stress-induced cellular damage, in comparison with WG extract (WGE) and RG extract (RGE) in a cell culture model. Ethanolic extracts of WG, RG, and BG were used to evaluate ginsenoside profiles, total polyphenols, flavonoid contents, and antioxidant activity. Using AML-12 cells treated with H(2)O(2), the protective effects of WGE, RGE, and BGE on cellular redox status, DNA, protein, lipid damage, and apoptosis levels were investigated. RESULTS: BGE exhibited significantly enhanced antioxidant potential, as well as total flavonoid and polyphenol contents. ATP levels were significantly higher in BGE-treated cells than in control; ROS generation and glutathione disulfide levels were lower but glutathione (GSH) and NADPH levels were higher in BGE-treated cells than in other groups. Pretreatment with BGE inhibited apoptosis and therefore protected cells from oxidative stress-induced cellular damage, probably through ROS scavenging. CONCLUSION: Collectively, our results demonstrate that BGE protects AML-12 cells from oxidative stress-induced cellular damages more effectively than WGE or RGE, through ROS scavenging, maintenance of redox status, and activation of the antioxidant defense system.
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spelling pubmed-64374682019-04-11 Ameliorative effect of black ginseng extract against oxidative stress-induced cellular damages in mouse hepatocytes Choudhry, Qaisra Naheed Kim, Jun Ho Cho, Hyung Taek Heo, Wan Lee, Jeong-Jun Lee, Jin Hyup Kim, Young Jun J Ginseng Res Research Article BACKGROUND: Oxidative stress induces the production of reactive oxygen species (ROS), which play important causative roles in various pathological conditions. Black ginseng (BG), a type of steam-processed ginseng, has drawn significant attention due to its biological activity, and is more potent than white ginseng (WG) or red ginseng (RG). METHODS: We evaluated the protective effects of BG extract (BGE) against oxidative stress-induced cellular damage, in comparison with WG extract (WGE) and RG extract (RGE) in a cell culture model. Ethanolic extracts of WG, RG, and BG were used to evaluate ginsenoside profiles, total polyphenols, flavonoid contents, and antioxidant activity. Using AML-12 cells treated with H(2)O(2), the protective effects of WGE, RGE, and BGE on cellular redox status, DNA, protein, lipid damage, and apoptosis levels were investigated. RESULTS: BGE exhibited significantly enhanced antioxidant potential, as well as total flavonoid and polyphenol contents. ATP levels were significantly higher in BGE-treated cells than in control; ROS generation and glutathione disulfide levels were lower but glutathione (GSH) and NADPH levels were higher in BGE-treated cells than in other groups. Pretreatment with BGE inhibited apoptosis and therefore protected cells from oxidative stress-induced cellular damage, probably through ROS scavenging. CONCLUSION: Collectively, our results demonstrate that BGE protects AML-12 cells from oxidative stress-induced cellular damages more effectively than WGE or RGE, through ROS scavenging, maintenance of redox status, and activation of the antioxidant defense system. Elsevier 2019-04 2017-10-21 /pmc/articles/PMC6437468/ /pubmed/30976158 http://dx.doi.org/10.1016/j.jgr.2017.10.003 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
Choudhry, Qaisra Naheed
Kim, Jun Ho
Cho, Hyung Taek
Heo, Wan
Lee, Jeong-Jun
Lee, Jin Hyup
Kim, Young Jun
Ameliorative effect of black ginseng extract against oxidative stress-induced cellular damages in mouse hepatocytes
title Ameliorative effect of black ginseng extract against oxidative stress-induced cellular damages in mouse hepatocytes
title_full Ameliorative effect of black ginseng extract against oxidative stress-induced cellular damages in mouse hepatocytes
title_fullStr Ameliorative effect of black ginseng extract against oxidative stress-induced cellular damages in mouse hepatocytes
title_full_unstemmed Ameliorative effect of black ginseng extract against oxidative stress-induced cellular damages in mouse hepatocytes
title_short Ameliorative effect of black ginseng extract against oxidative stress-induced cellular damages in mouse hepatocytes
title_sort ameliorative effect of black ginseng extract against oxidative stress-induced cellular damages in mouse hepatocytes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6437468/
https://www.ncbi.nlm.nih.gov/pubmed/30976158
http://dx.doi.org/10.1016/j.jgr.2017.10.003
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