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Oat (Avena sativa) Extract against Oxidative Stress-Induced Apoptosis in Human Keratinocytes

Oat (Avena sativa) is well known for its various health benefits. The protective effect of oat extract against oxidative stress-induced apoptosis in human keratinocytes HaCaT was determined. First, extracts of two varieties of oat, Daeyang and Choyang, were analyzed for fat-soluble antioxidants such...

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Autores principales: Song, Sooji, Lee, Yoon-Mi, Lee, Yu Young, Yeum, Kyung-Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8464938/
https://www.ncbi.nlm.nih.gov/pubmed/34577035
http://dx.doi.org/10.3390/molecules26185564
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author Song, Sooji
Lee, Yoon-Mi
Lee, Yu Young
Yeum, Kyung-Jin
author_facet Song, Sooji
Lee, Yoon-Mi
Lee, Yu Young
Yeum, Kyung-Jin
author_sort Song, Sooji
collection PubMed
description Oat (Avena sativa) is well known for its various health benefits. The protective effect of oat extract against oxidative stress-induced apoptosis in human keratinocytes HaCaT was determined. First, extracts of two varieties of oat, Daeyang and Choyang, were analyzed for fat-soluble antioxidants such as α-tocotrienol, γ-oryzanols, lutein and zeaxanthin using an UPLC system and for antioxidant activity using a DPPH assay. Specifically, an 80% ethanol extract of Daeyang oat (Avena sativa cv. Daeyang), which had high amounts of antioxidants and potent radical scavenging activity, was further evaluated for protective effect against oxidative stress-induced cell death, intracellular reactive oxygen species levels, the phosphorylation of DNA damage mediating genes such as H2AX, checkpoint kinase 1 and 2, and p53 and the activation of apoptotic genes such as cleaved caspase-3 and 7 and poly (ADP-ribose) polymerase in HaCaT cells. The Daeyang and Choyang oat 80% ethanol extracts had 26.9 and 24.1 mg/100 g γ-oryzanols, 7.69 and 8.38 mg/100 g α-tocotrienol, 1.25 and 0.34 mg/100 g of lutein and 1.20 and 0.17 mg/100 g of zeaxanthin, respectively. The oat 80% ethanol extract treatment (Avena sativa cv. Daeyang) had a protective effect on oxidative stress-induced cell death in HaCaT cells. In addition, the oat 80% ethanol extracts led to a significant decrease in the intracellular ROS level at a concentration of 50–200 μg/mL, the attenuation of DNA damage mediating genes and the inhibition of apoptotic caspase activities in a dose dependent manner (50–200 μg/mL). Thus, the current study indicates that an oat (Avena sativa cv. Daeyang) extract rich in antioxidants, such as polyphenols, avenanthramides, γ-oryzanols, tocotrienols and carotenoids, has a protective role against oxidative stress-induced keratinocyte injuries and that oat may a useful source for oxidative stress-associated skin damage.
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spelling pubmed-84649382021-09-27 Oat (Avena sativa) Extract against Oxidative Stress-Induced Apoptosis in Human Keratinocytes Song, Sooji Lee, Yoon-Mi Lee, Yu Young Yeum, Kyung-Jin Molecules Article Oat (Avena sativa) is well known for its various health benefits. The protective effect of oat extract against oxidative stress-induced apoptosis in human keratinocytes HaCaT was determined. First, extracts of two varieties of oat, Daeyang and Choyang, were analyzed for fat-soluble antioxidants such as α-tocotrienol, γ-oryzanols, lutein and zeaxanthin using an UPLC system and for antioxidant activity using a DPPH assay. Specifically, an 80% ethanol extract of Daeyang oat (Avena sativa cv. Daeyang), which had high amounts of antioxidants and potent radical scavenging activity, was further evaluated for protective effect against oxidative stress-induced cell death, intracellular reactive oxygen species levels, the phosphorylation of DNA damage mediating genes such as H2AX, checkpoint kinase 1 and 2, and p53 and the activation of apoptotic genes such as cleaved caspase-3 and 7 and poly (ADP-ribose) polymerase in HaCaT cells. The Daeyang and Choyang oat 80% ethanol extracts had 26.9 and 24.1 mg/100 g γ-oryzanols, 7.69 and 8.38 mg/100 g α-tocotrienol, 1.25 and 0.34 mg/100 g of lutein and 1.20 and 0.17 mg/100 g of zeaxanthin, respectively. The oat 80% ethanol extract treatment (Avena sativa cv. Daeyang) had a protective effect on oxidative stress-induced cell death in HaCaT cells. In addition, the oat 80% ethanol extracts led to a significant decrease in the intracellular ROS level at a concentration of 50–200 μg/mL, the attenuation of DNA damage mediating genes and the inhibition of apoptotic caspase activities in a dose dependent manner (50–200 μg/mL). Thus, the current study indicates that an oat (Avena sativa cv. Daeyang) extract rich in antioxidants, such as polyphenols, avenanthramides, γ-oryzanols, tocotrienols and carotenoids, has a protective role against oxidative stress-induced keratinocyte injuries and that oat may a useful source for oxidative stress-associated skin damage. MDPI 2021-09-13 /pmc/articles/PMC8464938/ /pubmed/34577035 http://dx.doi.org/10.3390/molecules26185564 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Song, Sooji
Lee, Yoon-Mi
Lee, Yu Young
Yeum, Kyung-Jin
Oat (Avena sativa) Extract against Oxidative Stress-Induced Apoptosis in Human Keratinocytes
title Oat (Avena sativa) Extract against Oxidative Stress-Induced Apoptosis in Human Keratinocytes
title_full Oat (Avena sativa) Extract against Oxidative Stress-Induced Apoptosis in Human Keratinocytes
title_fullStr Oat (Avena sativa) Extract against Oxidative Stress-Induced Apoptosis in Human Keratinocytes
title_full_unstemmed Oat (Avena sativa) Extract against Oxidative Stress-Induced Apoptosis in Human Keratinocytes
title_short Oat (Avena sativa) Extract against Oxidative Stress-Induced Apoptosis in Human Keratinocytes
title_sort oat (avena sativa) extract against oxidative stress-induced apoptosis in human keratinocytes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8464938/
https://www.ncbi.nlm.nih.gov/pubmed/34577035
http://dx.doi.org/10.3390/molecules26185564
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