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Protective effects of five compounds from Livistona chinensis R. Brown leaves against hypoxia/reoxygenation, H(2)O(2), or adriamycin-induced injury in H9c2 cells

Purpose: Discovering new antimyocardial ischemia drug candidates that are highly efficient, have low toxicity, and originate from natural products is a popular trend for new cardiovascular drug development at present. The ethanol extract of Livistona chinensis leaves showed a favorable antioxidant a...

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Detalles Bibliográficos
Autores principales: Li, Shaoguang, Luo, Shaohong, Chen, Hao, Zheng, Yanjie, Lin, Liqing, Yao, Hong, Lin, Xinhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2019
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6514125/
https://www.ncbi.nlm.nih.gov/pubmed/31190736
http://dx.doi.org/10.2147/DDDT.S201816
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author Li, Shaoguang
Luo, Shaohong
Chen, Hao
Zheng, Yanjie
Lin, Liqing
Yao, Hong
Lin, Xinhua
author_facet Li, Shaoguang
Luo, Shaohong
Chen, Hao
Zheng, Yanjie
Lin, Liqing
Yao, Hong
Lin, Xinhua
author_sort Li, Shaoguang
collection PubMed
description Purpose: Discovering new antimyocardial ischemia drug candidates that are highly efficient, have low toxicity, and originate from natural products is a popular trend for new cardiovascular drug development at present. The ethanol extract of Livistona chinensis leaves showed a favorable antioxidant activity in our preliminary screening test. This study aims to screen out antioxidants from the herb leaves further and evaluate their efficacy in acute myocardial ischemia treatment at the cellular level. Materials and methods: Guided with online 1, 1-diphenyl-2-picrylhydrazyl (DPPH)–high-performance liquid chromatography (HPLC) screening, antioxidants were first separated and isolated from the ethanol extract of L. chinensis leaves by preparative-HPLC. Subsequently, offline DPPH approach was used to validate the free radical scavenging activity of the components. Ultimately, the resulting antioxidants were evaluated against the hypoxia/reoxygenation (H/R)-, H(2)O(2)-, or adriamycin (ADM)-induced injury in H9c2 cells to verify their cardioprotective effects in vitro. Results: Five antioxidant ingredients, namely, orientin, isoorientin, vitexin, isovitexin, and tricin, were quickly distinguished and isolated from L. chinensis leaves. The IC(50) values of these ingredients were further examined by offline DPPH assay, as follows: 15.51±0.22, 6.64±0.38, 11.86±0.24, 8.89±0.66, and 31.86±0.24 μg/mL, respectively. Out of these ingredients, isoorientin showed the strongest antioxidation, which was equivalent to that of the positive control drug (vitamin C, IC(50): 6.99±0.62 μg/mL). Using H/R-, H(2)O(2)-, and ADM-induced H9c2 cell injury models, the five ingredients had different extents of cardioprotective effects in vitro. In particular, isoorientin showed the strongest protection. All the five ingredients also showed insignificant cytotoxic effect to normal H9c2 cells. Conclusion: The ethanol extract of L. chinensis leaves contained five antioxidants with low cardiac cytotoxicity. Isoorientin possessed the strongest antioxidation, which can predominantly account for the myocardial protection effects within the extract.
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spelling pubmed-65141252019-06-12 Protective effects of five compounds from Livistona chinensis R. Brown leaves against hypoxia/reoxygenation, H(2)O(2), or adriamycin-induced injury in H9c2 cells Li, Shaoguang Luo, Shaohong Chen, Hao Zheng, Yanjie Lin, Liqing Yao, Hong Lin, Xinhua Drug Des Devel Ther Original Research Purpose: Discovering new antimyocardial ischemia drug candidates that are highly efficient, have low toxicity, and originate from natural products is a popular trend for new cardiovascular drug development at present. The ethanol extract of Livistona chinensis leaves showed a favorable antioxidant activity in our preliminary screening test. This study aims to screen out antioxidants from the herb leaves further and evaluate their efficacy in acute myocardial ischemia treatment at the cellular level. Materials and methods: Guided with online 1, 1-diphenyl-2-picrylhydrazyl (DPPH)–high-performance liquid chromatography (HPLC) screening, antioxidants were first separated and isolated from the ethanol extract of L. chinensis leaves by preparative-HPLC. Subsequently, offline DPPH approach was used to validate the free radical scavenging activity of the components. Ultimately, the resulting antioxidants were evaluated against the hypoxia/reoxygenation (H/R)-, H(2)O(2)-, or adriamycin (ADM)-induced injury in H9c2 cells to verify their cardioprotective effects in vitro. Results: Five antioxidant ingredients, namely, orientin, isoorientin, vitexin, isovitexin, and tricin, were quickly distinguished and isolated from L. chinensis leaves. The IC(50) values of these ingredients were further examined by offline DPPH assay, as follows: 15.51±0.22, 6.64±0.38, 11.86±0.24, 8.89±0.66, and 31.86±0.24 μg/mL, respectively. Out of these ingredients, isoorientin showed the strongest antioxidation, which was equivalent to that of the positive control drug (vitamin C, IC(50): 6.99±0.62 μg/mL). Using H/R-, H(2)O(2)-, and ADM-induced H9c2 cell injury models, the five ingredients had different extents of cardioprotective effects in vitro. In particular, isoorientin showed the strongest protection. All the five ingredients also showed insignificant cytotoxic effect to normal H9c2 cells. Conclusion: The ethanol extract of L. chinensis leaves contained five antioxidants with low cardiac cytotoxicity. Isoorientin possessed the strongest antioxidation, which can predominantly account for the myocardial protection effects within the extract. Dove 2019-05-08 /pmc/articles/PMC6514125/ /pubmed/31190736 http://dx.doi.org/10.2147/DDDT.S201816 Text en © 2019 Li et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Li, Shaoguang
Luo, Shaohong
Chen, Hao
Zheng, Yanjie
Lin, Liqing
Yao, Hong
Lin, Xinhua
Protective effects of five compounds from Livistona chinensis R. Brown leaves against hypoxia/reoxygenation, H(2)O(2), or adriamycin-induced injury in H9c2 cells
title Protective effects of five compounds from Livistona chinensis R. Brown leaves against hypoxia/reoxygenation, H(2)O(2), or adriamycin-induced injury in H9c2 cells
title_full Protective effects of five compounds from Livistona chinensis R. Brown leaves against hypoxia/reoxygenation, H(2)O(2), or adriamycin-induced injury in H9c2 cells
title_fullStr Protective effects of five compounds from Livistona chinensis R. Brown leaves against hypoxia/reoxygenation, H(2)O(2), or adriamycin-induced injury in H9c2 cells
title_full_unstemmed Protective effects of five compounds from Livistona chinensis R. Brown leaves against hypoxia/reoxygenation, H(2)O(2), or adriamycin-induced injury in H9c2 cells
title_short Protective effects of five compounds from Livistona chinensis R. Brown leaves against hypoxia/reoxygenation, H(2)O(2), or adriamycin-induced injury in H9c2 cells
title_sort protective effects of five compounds from livistona chinensis r. brown leaves against hypoxia/reoxygenation, h(2)o(2), or adriamycin-induced injury in h9c2 cells
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6514125/
https://www.ncbi.nlm.nih.gov/pubmed/31190736
http://dx.doi.org/10.2147/DDDT.S201816
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