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Protecting HaCaT cells from ionizing radiation using persimmon tannin-Aloe gel composite

CONTEXT: Persimmon tannin (extract of Diospyros kaki L.f [Ebenaceae]) and Aloe gel (extract of Aloe vera (L.) Burm.f. [Asphodelaceae]) are known as anti-radiation agents. However, radiation resistance of the persimmon tannin-Aloe gel composite remains inconclusive. OBJECTIVE: To investigate the capa...

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Autores principales: Qian, Xi, Wang, Zhongmin, Ning, Jinliang, Qin, Chaoke, Gao, Lin, He, Na, Lin, Dahong, Zhou, Zhide, Li, Guiyin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8641672/
https://www.ncbi.nlm.nih.gov/pubmed/32476533
http://dx.doi.org/10.1080/13880209.2020.1767158
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author Qian, Xi
Wang, Zhongmin
Ning, Jinliang
Qin, Chaoke
Gao, Lin
He, Na
Lin, Dahong
Zhou, Zhide
Li, Guiyin
author_facet Qian, Xi
Wang, Zhongmin
Ning, Jinliang
Qin, Chaoke
Gao, Lin
He, Na
Lin, Dahong
Zhou, Zhide
Li, Guiyin
author_sort Qian, Xi
collection PubMed
description CONTEXT: Persimmon tannin (extract of Diospyros kaki L.f [Ebenaceae]) and Aloe gel (extract of Aloe vera (L.) Burm.f. [Asphodelaceae]) are known as anti-radiation agents. However, radiation resistance of the persimmon tannin-Aloe gel composite remains inconclusive. OBJECTIVE: To investigate the capacity of the persimmon tannin-Aloe gel composite to protect against ionising radiation at the cellular level. MATERIALS AND METHODS: HaCaT (human epidermal keratinocytes) cells were pre-treated with PT-A-1 (the mass ratio of persimmon tannin and Aloe gel was 2:1) or the single component (persimmon tannin or Aloe gel) at various concentrations (0, 50, 100, 200, 400, 800 μg/mL. Control group: medium with no HaCaT cells), and then radiated with X-rays (radiation dose: 4, 8, 12, 16, and 20 Gy). Cell viability, cell apoptosis, and radiation-induced intracellular reactive oxygen species (ROS) generation were analysed by CCK-8, Hoechst 33258 staining/flow cytometry, and 2′,7′-dichlorfluorescein diacetate (DCFH-DA) assay, respectively, for 12 or 24 h incubation after radiation. RESULTS: The optimal radiation dose and post-radiation incubation period were determined to be 8 Gy and 12 h. CCK-8 activity detection showed that the cell activity was 77.85% (p < 0.05, IC(50) = 55.67 μg/mL). The apoptotic rate was the lowest (4.32%) at 200 μg/mL of PT-A-1 towards HaCaT cells. ROS production was the most effectively suppressed by 200 μg/mL PT-A-1 towards HaCaT cells. DISCUSSION AND CONCLUSIONS: The persimmon tannin-Aloe gel composite has good radioprotective effect, and which will facilitate its clinic application as a potential natural anti-radiation agent in future.
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spelling pubmed-86416722021-12-04 Protecting HaCaT cells from ionizing radiation using persimmon tannin-Aloe gel composite Qian, Xi Wang, Zhongmin Ning, Jinliang Qin, Chaoke Gao, Lin He, Na Lin, Dahong Zhou, Zhide Li, Guiyin Pharm Biol Research Article CONTEXT: Persimmon tannin (extract of Diospyros kaki L.f [Ebenaceae]) and Aloe gel (extract of Aloe vera (L.) Burm.f. [Asphodelaceae]) are known as anti-radiation agents. However, radiation resistance of the persimmon tannin-Aloe gel composite remains inconclusive. OBJECTIVE: To investigate the capacity of the persimmon tannin-Aloe gel composite to protect against ionising radiation at the cellular level. MATERIALS AND METHODS: HaCaT (human epidermal keratinocytes) cells were pre-treated with PT-A-1 (the mass ratio of persimmon tannin and Aloe gel was 2:1) or the single component (persimmon tannin or Aloe gel) at various concentrations (0, 50, 100, 200, 400, 800 μg/mL. Control group: medium with no HaCaT cells), and then radiated with X-rays (radiation dose: 4, 8, 12, 16, and 20 Gy). Cell viability, cell apoptosis, and radiation-induced intracellular reactive oxygen species (ROS) generation were analysed by CCK-8, Hoechst 33258 staining/flow cytometry, and 2′,7′-dichlorfluorescein diacetate (DCFH-DA) assay, respectively, for 12 or 24 h incubation after radiation. RESULTS: The optimal radiation dose and post-radiation incubation period were determined to be 8 Gy and 12 h. CCK-8 activity detection showed that the cell activity was 77.85% (p < 0.05, IC(50) = 55.67 μg/mL). The apoptotic rate was the lowest (4.32%) at 200 μg/mL of PT-A-1 towards HaCaT cells. ROS production was the most effectively suppressed by 200 μg/mL PT-A-1 towards HaCaT cells. DISCUSSION AND CONCLUSIONS: The persimmon tannin-Aloe gel composite has good radioprotective effect, and which will facilitate its clinic application as a potential natural anti-radiation agent in future. Taylor & Francis 2020-06-01 /pmc/articles/PMC8641672/ /pubmed/32476533 http://dx.doi.org/10.1080/13880209.2020.1767158 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Qian, Xi
Wang, Zhongmin
Ning, Jinliang
Qin, Chaoke
Gao, Lin
He, Na
Lin, Dahong
Zhou, Zhide
Li, Guiyin
Protecting HaCaT cells from ionizing radiation using persimmon tannin-Aloe gel composite
title Protecting HaCaT cells from ionizing radiation using persimmon tannin-Aloe gel composite
title_full Protecting HaCaT cells from ionizing radiation using persimmon tannin-Aloe gel composite
title_fullStr Protecting HaCaT cells from ionizing radiation using persimmon tannin-Aloe gel composite
title_full_unstemmed Protecting HaCaT cells from ionizing radiation using persimmon tannin-Aloe gel composite
title_short Protecting HaCaT cells from ionizing radiation using persimmon tannin-Aloe gel composite
title_sort protecting hacat cells from ionizing radiation using persimmon tannin-aloe gel composite
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8641672/
https://www.ncbi.nlm.nih.gov/pubmed/32476533
http://dx.doi.org/10.1080/13880209.2020.1767158
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