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Resveratrol-loaded Nanoparticles Induce Antioxidant Activity against Oxidative Stress

Resveratrol acts as a free radical scavenger and a potent antioxidant in the inhibition of numerous reactive oxygen species (ROS). The function of resveratrol and resveratrol-loaded nanoparticles in protecting human lung cancer cells (A549) against hydrogen peroxide was investigated in this study. T...

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Autores principales: Kim, Jae-Hwan, Park, Eun-Young, Ha, Ho-Kyung, Jo, Chan-Mi, Lee, Won-Jae, Lee, Sung Sill, Kim, Jin Wook
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Asian-Australasian Association of Animal Production Societies (AAAP) and Korean Society of Animal Science and Technology (KSAST) 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4698710/
https://www.ncbi.nlm.nih.gov/pubmed/26732454
http://dx.doi.org/10.5713/ajas.15.0774
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author Kim, Jae-Hwan
Park, Eun-Young
Ha, Ho-Kyung
Jo, Chan-Mi
Lee, Won-Jae
Lee, Sung Sill
Kim, Jin Wook
author_facet Kim, Jae-Hwan
Park, Eun-Young
Ha, Ho-Kyung
Jo, Chan-Mi
Lee, Won-Jae
Lee, Sung Sill
Kim, Jin Wook
author_sort Kim, Jae-Hwan
collection PubMed
description Resveratrol acts as a free radical scavenger and a potent antioxidant in the inhibition of numerous reactive oxygen species (ROS). The function of resveratrol and resveratrol-loaded nanoparticles in protecting human lung cancer cells (A549) against hydrogen peroxide was investigated in this study. The 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid (ABTS) assay was performed to evaluate the antioxidant properties. Resveratrol had substantially high antioxidant capacity (trolox equivalent antioxidant capacity value) compared to trolox and vitamin E since the concentration of resveratrol was more than 50 μM. Nanoparticles prepared from β-lactoglobulin (β-lg) were successfully developed. The β-lg nanoparticle showed 60 to 146 nm diameter in size with negatively charged surface. Non-cytotoxicity was observed in Caco-2 cells treated with β-lg nanoparticles. Fluorescein isothiocynate-conjugated β-lg nanoparticles were identified into the cell membrane of Caco-2 cells, indicating that nanoparticles can be used as a delivery system. Hydrogen peroxide caused accumulation of ROS in a dose- and time-dependent manner. Resveratrol-loaded nanoparticles restored H(2)O(2)-induced ROS levels by induction of cellular uptake of resveratrol in A549 cells. Furthermore, resveratrol activated nuclear factor erythroid 2-related factor 2-Kelch ECH associating protein 1 (Nrf2-Keap1) signaling in A549 cells, thereby accumulation of Nrf2 abundance, as demonstrated by western blotting approach. Overall, these results may have implications for improvement of oxidative stress in treatment with nanoparticles as a biodegradable and non-toxic delivery carrier of bioactive compounds.
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spelling pubmed-46987102016-02-01 Resveratrol-loaded Nanoparticles Induce Antioxidant Activity against Oxidative Stress Kim, Jae-Hwan Park, Eun-Young Ha, Ho-Kyung Jo, Chan-Mi Lee, Won-Jae Lee, Sung Sill Kim, Jin Wook Asian-Australas J Anim Sci Article Resveratrol acts as a free radical scavenger and a potent antioxidant in the inhibition of numerous reactive oxygen species (ROS). The function of resveratrol and resveratrol-loaded nanoparticles in protecting human lung cancer cells (A549) against hydrogen peroxide was investigated in this study. The 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid (ABTS) assay was performed to evaluate the antioxidant properties. Resveratrol had substantially high antioxidant capacity (trolox equivalent antioxidant capacity value) compared to trolox and vitamin E since the concentration of resveratrol was more than 50 μM. Nanoparticles prepared from β-lactoglobulin (β-lg) were successfully developed. The β-lg nanoparticle showed 60 to 146 nm diameter in size with negatively charged surface. Non-cytotoxicity was observed in Caco-2 cells treated with β-lg nanoparticles. Fluorescein isothiocynate-conjugated β-lg nanoparticles were identified into the cell membrane of Caco-2 cells, indicating that nanoparticles can be used as a delivery system. Hydrogen peroxide caused accumulation of ROS in a dose- and time-dependent manner. Resveratrol-loaded nanoparticles restored H(2)O(2)-induced ROS levels by induction of cellular uptake of resveratrol in A549 cells. Furthermore, resveratrol activated nuclear factor erythroid 2-related factor 2-Kelch ECH associating protein 1 (Nrf2-Keap1) signaling in A549 cells, thereby accumulation of Nrf2 abundance, as demonstrated by western blotting approach. Overall, these results may have implications for improvement of oxidative stress in treatment with nanoparticles as a biodegradable and non-toxic delivery carrier of bioactive compounds. Asian-Australasian Association of Animal Production Societies (AAAP) and Korean Society of Animal Science and Technology (KSAST) 2016-02 2015-12-01 /pmc/articles/PMC4698710/ /pubmed/26732454 http://dx.doi.org/10.5713/ajas.15.0774 Text en Copyright © 2016 by Asian-Australasian Journal of Animal Sciences This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License http://creativecommons.org/licenses/by-nc/3.0/ which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Kim, Jae-Hwan
Park, Eun-Young
Ha, Ho-Kyung
Jo, Chan-Mi
Lee, Won-Jae
Lee, Sung Sill
Kim, Jin Wook
Resveratrol-loaded Nanoparticles Induce Antioxidant Activity against Oxidative Stress
title Resveratrol-loaded Nanoparticles Induce Antioxidant Activity against Oxidative Stress
title_full Resveratrol-loaded Nanoparticles Induce Antioxidant Activity against Oxidative Stress
title_fullStr Resveratrol-loaded Nanoparticles Induce Antioxidant Activity against Oxidative Stress
title_full_unstemmed Resveratrol-loaded Nanoparticles Induce Antioxidant Activity against Oxidative Stress
title_short Resveratrol-loaded Nanoparticles Induce Antioxidant Activity against Oxidative Stress
title_sort resveratrol-loaded nanoparticles induce antioxidant activity against oxidative stress
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4698710/
https://www.ncbi.nlm.nih.gov/pubmed/26732454
http://dx.doi.org/10.5713/ajas.15.0774
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