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Biogenic selenium and its hepatoprotective activity

Elemental selenium nanoparticles (SeNPs) have multiple biological activities. In this study, we investigated the protective effects of biogenic SeNPs (BioSeNPs) on CCl(4)-induced liver damage in mice. The results showed that: (i) when compared to sodium selenite (SS), BioSeNPs has a similar tissue d...

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Autores principales: Li, Baozhen, Li, Dan, Jing, Weixin, Fan, Jinhua, Dahms, Hans-Uwe, Lee, Shao-Chin, Wang, Lan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5688085/
https://www.ncbi.nlm.nih.gov/pubmed/29142221
http://dx.doi.org/10.1038/s41598-017-13636-1
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author Li, Baozhen
Li, Dan
Jing, Weixin
Fan, Jinhua
Dahms, Hans-Uwe
Lee, Shao-Chin
Wang, Lan
author_facet Li, Baozhen
Li, Dan
Jing, Weixin
Fan, Jinhua
Dahms, Hans-Uwe
Lee, Shao-Chin
Wang, Lan
author_sort Li, Baozhen
collection PubMed
description Elemental selenium nanoparticles (SeNPs) have multiple biological activities. In this study, we investigated the protective effects of biogenic SeNPs (BioSeNPs) on CCl(4)-induced liver damage in mice. The results showed that: (i) when compared to sodium selenite (SS), BioSeNPs has a similar tissue distribution after intragastrical administration to mice; (ii) BioSeNPs and SS showed comparable efficacy in increasing the activities of glutathione peroxidase and thioredoxin reductase in liver cell lines, mice blood and liver; (iii) pretreatment with BioSeNPs inhibiting the elevation of activities of various enzymes significantly which included aspartate aminotransferase, alanine aminotransferase, alkaline phosphatase, lactate dehydrogenase and liver lipid peroxide (p < 0.05 or p < 0.01) in CCl(4)-treated mice; (iv) activities of antioxidant enzymes (superoxide dismutase, catalase, and glutathione peroxidase) were significantly increased (p < 0.05 or p < 0.01) after a pretreatment with BioSeNPs in CCl(4)-treated mice; (v) histopathological damages in the liver from CCl(4)-treated mice were ameliorated by a pretreatment with BioSeNPs. In conclusion, these results have shown that BioSeNPs is able to protect the liver from CCl(4)-induced hepatic damage via increasing the antioxidant capacity and inhibiting oxidative damage. BioSeNPs may have the potential to be used as a trace element food supplement inducing antioxidant bioactivities.
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spelling pubmed-56880852017-11-24 Biogenic selenium and its hepatoprotective activity Li, Baozhen Li, Dan Jing, Weixin Fan, Jinhua Dahms, Hans-Uwe Lee, Shao-Chin Wang, Lan Sci Rep Article Elemental selenium nanoparticles (SeNPs) have multiple biological activities. In this study, we investigated the protective effects of biogenic SeNPs (BioSeNPs) on CCl(4)-induced liver damage in mice. The results showed that: (i) when compared to sodium selenite (SS), BioSeNPs has a similar tissue distribution after intragastrical administration to mice; (ii) BioSeNPs and SS showed comparable efficacy in increasing the activities of glutathione peroxidase and thioredoxin reductase in liver cell lines, mice blood and liver; (iii) pretreatment with BioSeNPs inhibiting the elevation of activities of various enzymes significantly which included aspartate aminotransferase, alanine aminotransferase, alkaline phosphatase, lactate dehydrogenase and liver lipid peroxide (p < 0.05 or p < 0.01) in CCl(4)-treated mice; (iv) activities of antioxidant enzymes (superoxide dismutase, catalase, and glutathione peroxidase) were significantly increased (p < 0.05 or p < 0.01) after a pretreatment with BioSeNPs in CCl(4)-treated mice; (v) histopathological damages in the liver from CCl(4)-treated mice were ameliorated by a pretreatment with BioSeNPs. In conclusion, these results have shown that BioSeNPs is able to protect the liver from CCl(4)-induced hepatic damage via increasing the antioxidant capacity and inhibiting oxidative damage. BioSeNPs may have the potential to be used as a trace element food supplement inducing antioxidant bioactivities. Nature Publishing Group UK 2017-11-15 /pmc/articles/PMC5688085/ /pubmed/29142221 http://dx.doi.org/10.1038/s41598-017-13636-1 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Li, Baozhen
Li, Dan
Jing, Weixin
Fan, Jinhua
Dahms, Hans-Uwe
Lee, Shao-Chin
Wang, Lan
Biogenic selenium and its hepatoprotective activity
title Biogenic selenium and its hepatoprotective activity
title_full Biogenic selenium and its hepatoprotective activity
title_fullStr Biogenic selenium and its hepatoprotective activity
title_full_unstemmed Biogenic selenium and its hepatoprotective activity
title_short Biogenic selenium and its hepatoprotective activity
title_sort biogenic selenium and its hepatoprotective activity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5688085/
https://www.ncbi.nlm.nih.gov/pubmed/29142221
http://dx.doi.org/10.1038/s41598-017-13636-1
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