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Effects of 7-MEGA(TM) 500 on Oxidative Stress, Inflammation, and Skin Regeneration in H(2)O(2)-Treated Skin Cells

Environmental stimuli can lead to the excessive accumulation of reactive oxygen species (ROS), which is one of the risk factors for premature skin aging. Here, we investigated the protective effects of 7-MEGA(TM) 500 (50% palmitoleic acid, 7-MEGA) against oxidative stress-induced cellular damage and...

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Autores principales: Song, In-Bong, Gu, Hyejung, Han, Hye-Ju, Lee, Na-Young, Cha, Ji-Yun, Son, Yeon-Kyong, Kwon, Jungkee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Toxicology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5903135/
https://www.ncbi.nlm.nih.gov/pubmed/29686772
http://dx.doi.org/10.5487/TR.2018.34.2.103
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author Song, In-Bong
Gu, Hyejung
Han, Hye-Ju
Lee, Na-Young
Cha, Ji-Yun
Son, Yeon-Kyong
Kwon, Jungkee
author_facet Song, In-Bong
Gu, Hyejung
Han, Hye-Ju
Lee, Na-Young
Cha, Ji-Yun
Son, Yeon-Kyong
Kwon, Jungkee
author_sort Song, In-Bong
collection PubMed
description Environmental stimuli can lead to the excessive accumulation of reactive oxygen species (ROS), which is one of the risk factors for premature skin aging. Here, we investigated the protective effects of 7-MEGA(TM) 500 (50% palmitoleic acid, 7-MEGA) against oxidative stress-induced cellular damage and its underlying therapeutic mechanisms in the HaCaT human skin keratinocyte cell line (HaCaT cells). Our results showed that treatment with 7-MEGA prior to hydrogen peroxide (H(2)O(2))-induced damage significantly increased the viability of HaCaT cells. 7-MEGA effectively attenuated generation of H(2)O(2)-induced reactive oxygen species (ROS), and inhibited H(2)O(2)-induced inflammatory factors, such as prostaglandin E(2) (PGE(2)), tumor necrosis factor-α (TNF-α), and interleukin-1β (IL-1β). In addition, cells treated with 7-MEGA exhibited significantly decreased expression of matrix metalloproteinase-1 (MMP-1) and increased expression of procollagen type 1 (PCOL1) and Elastin against oxidative stress by H(2)O(2). Interestingly, these protective activities of 7-MEGA were similar in scope and of a higher magnitude than those seen with 98.5% palmitoleic acid (PA) obtained from Sigma when given at the same concentration (100 nL/mL). According to our data, 7-MEGA is able to protect HaCaT cells from H(2)O(2)-induced damage through inhibiting cellular oxidative stress and inflammation. Moreover, 7-MEGA may affect skin elasticity maintenance and improve skin wrinkles. These findings indicate that 7-MEGA may be useful as a food supplement for skin health.
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spelling pubmed-59031352018-04-23 Effects of 7-MEGA(TM) 500 on Oxidative Stress, Inflammation, and Skin Regeneration in H(2)O(2)-Treated Skin Cells Song, In-Bong Gu, Hyejung Han, Hye-Ju Lee, Na-Young Cha, Ji-Yun Son, Yeon-Kyong Kwon, Jungkee Toxicol Res Original Article Environmental stimuli can lead to the excessive accumulation of reactive oxygen species (ROS), which is one of the risk factors for premature skin aging. Here, we investigated the protective effects of 7-MEGA(TM) 500 (50% palmitoleic acid, 7-MEGA) against oxidative stress-induced cellular damage and its underlying therapeutic mechanisms in the HaCaT human skin keratinocyte cell line (HaCaT cells). Our results showed that treatment with 7-MEGA prior to hydrogen peroxide (H(2)O(2))-induced damage significantly increased the viability of HaCaT cells. 7-MEGA effectively attenuated generation of H(2)O(2)-induced reactive oxygen species (ROS), and inhibited H(2)O(2)-induced inflammatory factors, such as prostaglandin E(2) (PGE(2)), tumor necrosis factor-α (TNF-α), and interleukin-1β (IL-1β). In addition, cells treated with 7-MEGA exhibited significantly decreased expression of matrix metalloproteinase-1 (MMP-1) and increased expression of procollagen type 1 (PCOL1) and Elastin against oxidative stress by H(2)O(2). Interestingly, these protective activities of 7-MEGA were similar in scope and of a higher magnitude than those seen with 98.5% palmitoleic acid (PA) obtained from Sigma when given at the same concentration (100 nL/mL). According to our data, 7-MEGA is able to protect HaCaT cells from H(2)O(2)-induced damage through inhibiting cellular oxidative stress and inflammation. Moreover, 7-MEGA may affect skin elasticity maintenance and improve skin wrinkles. These findings indicate that 7-MEGA may be useful as a food supplement for skin health. Korean Society of Toxicology 2018-04 2018-04-15 /pmc/articles/PMC5903135/ /pubmed/29686772 http://dx.doi.org/10.5487/TR.2018.34.2.103 Text en Copyright © 2018 The Korean Society Of Toxicology http://creativecommons.org/licenses/by-nc/3.0 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 non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Song, In-Bong
Gu, Hyejung
Han, Hye-Ju
Lee, Na-Young
Cha, Ji-Yun
Son, Yeon-Kyong
Kwon, Jungkee
Effects of 7-MEGA(TM) 500 on Oxidative Stress, Inflammation, and Skin Regeneration in H(2)O(2)-Treated Skin Cells
title Effects of 7-MEGA(TM) 500 on Oxidative Stress, Inflammation, and Skin Regeneration in H(2)O(2)-Treated Skin Cells
title_full Effects of 7-MEGA(TM) 500 on Oxidative Stress, Inflammation, and Skin Regeneration in H(2)O(2)-Treated Skin Cells
title_fullStr Effects of 7-MEGA(TM) 500 on Oxidative Stress, Inflammation, and Skin Regeneration in H(2)O(2)-Treated Skin Cells
title_full_unstemmed Effects of 7-MEGA(TM) 500 on Oxidative Stress, Inflammation, and Skin Regeneration in H(2)O(2)-Treated Skin Cells
title_short Effects of 7-MEGA(TM) 500 on Oxidative Stress, Inflammation, and Skin Regeneration in H(2)O(2)-Treated Skin Cells
title_sort effects of 7-mega(tm) 500 on oxidative stress, inflammation, and skin regeneration in h(2)o(2)-treated skin cells
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5903135/
https://www.ncbi.nlm.nih.gov/pubmed/29686772
http://dx.doi.org/10.5487/TR.2018.34.2.103
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