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Improvement of Flavonoids in Lemon Seeds on Oxidative Damage of Human Embryonic Kidney 293T Cells Induced by H(2)O(2)

In this study, flavonoids in lemon seeds (FLS) were used to assess its improvement on the oxidative damage of human embryonic kidney 293T cells (HEK 293T cells) induced by H(2)O(2). In vitro experiments showed that the survival rates of HEK 293T cells treated with different flavonoid concentrations...

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Autores principales: Yang, Dingyi, Jiang, Yong, Wang, Yuqing, Lei, Qianqian, Zhao, Xin, Yi, Ruokun, Zhang, Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7189339/
https://www.ncbi.nlm.nih.gov/pubmed/32377296
http://dx.doi.org/10.1155/2020/3483519
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author Yang, Dingyi
Jiang, Yong
Wang, Yuqing
Lei, Qianqian
Zhao, Xin
Yi, Ruokun
Zhang, Xin
author_facet Yang, Dingyi
Jiang, Yong
Wang, Yuqing
Lei, Qianqian
Zhao, Xin
Yi, Ruokun
Zhang, Xin
author_sort Yang, Dingyi
collection PubMed
description In this study, flavonoids in lemon seeds (FLS) were used to assess its improvement on the oxidative damage of human embryonic kidney 293T cells (HEK 293T cells) induced by H(2)O(2). In vitro experiments showed that the survival rates of HEK 293T cells treated with different flavonoid concentrations (50 μg/mL, 100 μg/mL, and 150 μg/mL) exceeded 95%, indicating no significant toxic effect. Compared with the normal group, H(2)O(2) (0.3 mmol/L) resulted significantly in oxidative stress injury of HEK 293T cells. The survival rate of the damaged cells increased after treatment with flavonoids, and the survival rate of cells treated with a high concentration (150 μg/mL) of flavonoids was 76.2%. Flavonoids also effectively inhibited H(2)O(2)-induced apoptosis. At the same time, flavonoid treatment significantly reduced the malondialdehyde content in cells and increased the levels of catalase (CAT), superoxide dismutase (SOD), glutathione (GSH), and glutathione peroxidase (GSH-Px). Quantitative polymerase chain reaction (qPCR) and Western blot analysis also suggested that FLS upregulated mRNA and protein expressions of CAT, SOD (SOD1, SOD2), GSH (GSH1), and GSH-Px in H(2)O(2)-induced oxidative damage of HEK 293T cells. The high-performance liquid chromatography analysis demonstrated that FLS contained six compounds, including gallocatechin, caffeic acid, epicatechin, vitexin, quercetin, and hesperidin. FLS were proven to have a good antioxidant capacity in vitro and improve significantly the oxidative damage of HEK 293T cells induced by H(2)O(2). The biological activity value warrants investigation in additional studies.
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spelling pubmed-71893392020-05-06 Improvement of Flavonoids in Lemon Seeds on Oxidative Damage of Human Embryonic Kidney 293T Cells Induced by H(2)O(2) Yang, Dingyi Jiang, Yong Wang, Yuqing Lei, Qianqian Zhao, Xin Yi, Ruokun Zhang, Xin Oxid Med Cell Longev Research Article In this study, flavonoids in lemon seeds (FLS) were used to assess its improvement on the oxidative damage of human embryonic kidney 293T cells (HEK 293T cells) induced by H(2)O(2). In vitro experiments showed that the survival rates of HEK 293T cells treated with different flavonoid concentrations (50 μg/mL, 100 μg/mL, and 150 μg/mL) exceeded 95%, indicating no significant toxic effect. Compared with the normal group, H(2)O(2) (0.3 mmol/L) resulted significantly in oxidative stress injury of HEK 293T cells. The survival rate of the damaged cells increased after treatment with flavonoids, and the survival rate of cells treated with a high concentration (150 μg/mL) of flavonoids was 76.2%. Flavonoids also effectively inhibited H(2)O(2)-induced apoptosis. At the same time, flavonoid treatment significantly reduced the malondialdehyde content in cells and increased the levels of catalase (CAT), superoxide dismutase (SOD), glutathione (GSH), and glutathione peroxidase (GSH-Px). Quantitative polymerase chain reaction (qPCR) and Western blot analysis also suggested that FLS upregulated mRNA and protein expressions of CAT, SOD (SOD1, SOD2), GSH (GSH1), and GSH-Px in H(2)O(2)-induced oxidative damage of HEK 293T cells. The high-performance liquid chromatography analysis demonstrated that FLS contained six compounds, including gallocatechin, caffeic acid, epicatechin, vitexin, quercetin, and hesperidin. FLS were proven to have a good antioxidant capacity in vitro and improve significantly the oxidative damage of HEK 293T cells induced by H(2)O(2). The biological activity value warrants investigation in additional studies. Hindawi 2020-04-19 /pmc/articles/PMC7189339/ /pubmed/32377296 http://dx.doi.org/10.1155/2020/3483519 Text en Copyright © 2020 Dingyi Yang et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Yang, Dingyi
Jiang, Yong
Wang, Yuqing
Lei, Qianqian
Zhao, Xin
Yi, Ruokun
Zhang, Xin
Improvement of Flavonoids in Lemon Seeds on Oxidative Damage of Human Embryonic Kidney 293T Cells Induced by H(2)O(2)
title Improvement of Flavonoids in Lemon Seeds on Oxidative Damage of Human Embryonic Kidney 293T Cells Induced by H(2)O(2)
title_full Improvement of Flavonoids in Lemon Seeds on Oxidative Damage of Human Embryonic Kidney 293T Cells Induced by H(2)O(2)
title_fullStr Improvement of Flavonoids in Lemon Seeds on Oxidative Damage of Human Embryonic Kidney 293T Cells Induced by H(2)O(2)
title_full_unstemmed Improvement of Flavonoids in Lemon Seeds on Oxidative Damage of Human Embryonic Kidney 293T Cells Induced by H(2)O(2)
title_short Improvement of Flavonoids in Lemon Seeds on Oxidative Damage of Human Embryonic Kidney 293T Cells Induced by H(2)O(2)
title_sort improvement of flavonoids in lemon seeds on oxidative damage of human embryonic kidney 293t cells induced by h(2)o(2)
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7189339/
https://www.ncbi.nlm.nih.gov/pubmed/32377296
http://dx.doi.org/10.1155/2020/3483519
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