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Ulmus macrocarpa Hance Extracts Attenuated H(2)O(2) and UVB-Induced Skin Photo-Aging by Activating Antioxidant Enzymes and Inhibiting MAPK Pathways

To protect from reactive oxygen species (ROS) damages, skin cells have evolved to have antioxidant enzymes, such as copper and zinc-dependent superoxide dismutase (SOD1), mitochondrial manganese-dependent superoxide dismutase (SOD2), catalase (CAT), glutathione peroxidase (GPX), and glutathione redu...

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Autores principales: Choi, Sun-Il, Lee, Jin-Ha, Kim, Jae-Min, Jung, Tae-Dong, Cho, Bong-Yeon, Choi, Seung-Hyun, Lee, Dae-Won, Kim, Jinkyung, Kim, Jong-Yea, Lee, Ok-Hawn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5486023/
https://www.ncbi.nlm.nih.gov/pubmed/28587261
http://dx.doi.org/10.3390/ijms18061200
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author Choi, Sun-Il
Lee, Jin-Ha
Kim, Jae-Min
Jung, Tae-Dong
Cho, Bong-Yeon
Choi, Seung-Hyun
Lee, Dae-Won
Kim, Jinkyung
Kim, Jong-Yea
Lee, Ok-Hawn
author_facet Choi, Sun-Il
Lee, Jin-Ha
Kim, Jae-Min
Jung, Tae-Dong
Cho, Bong-Yeon
Choi, Seung-Hyun
Lee, Dae-Won
Kim, Jinkyung
Kim, Jong-Yea
Lee, Ok-Hawn
author_sort Choi, Sun-Il
collection PubMed
description To protect from reactive oxygen species (ROS) damages, skin cells have evolved to have antioxidant enzymes, such as copper and zinc-dependent superoxide dismutase (SOD1), mitochondrial manganese-dependent superoxide dismutase (SOD2), catalase (CAT), glutathione peroxidase (GPX), and glutathione reductase (GR), and suppressed the expression of matrix metalloproteinases (MMPs) through the mitogen-activated protein kinase (MAPK) signaling pathways, such as c-Jun N-terminal kinase (JNK) and p38. Bioactive compounds analyses were performed using a high-performance liquid chromatography-photodiode array detector (HPLC-PDA) system. The antioxidant activity of Ulmus macrocarpa Hance (UMH) extracts was estimated in vitro. The anti-aging activity of UMH extracts was estimated in vivo using the SKH-1 hairless mice. The UMH extracts reduced the H(2)O(2)-induced intracellular ROS production and the cell damages in human dermal fibroblasts (HDFs). Moreover, the H(2)O(2)-induced phosphorylation of JNK and p38 was detected in HDF and UMH extracts blocked the phosphorylation. These results suggest that UMH extracts can reduce the expression of MMPs and the reduced MMPs lead to the inhibition of collagen degradation. In addition, oral administration of the UMH extracts decreased the depth, thickness, and length of wrinkles on UVB exposed hairless mice. Therefore, UMH extracts play an advantage of the functional materials in antioxidant and anti-aging of skin.
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spelling pubmed-54860232017-06-29 Ulmus macrocarpa Hance Extracts Attenuated H(2)O(2) and UVB-Induced Skin Photo-Aging by Activating Antioxidant Enzymes and Inhibiting MAPK Pathways Choi, Sun-Il Lee, Jin-Ha Kim, Jae-Min Jung, Tae-Dong Cho, Bong-Yeon Choi, Seung-Hyun Lee, Dae-Won Kim, Jinkyung Kim, Jong-Yea Lee, Ok-Hawn Int J Mol Sci Article To protect from reactive oxygen species (ROS) damages, skin cells have evolved to have antioxidant enzymes, such as copper and zinc-dependent superoxide dismutase (SOD1), mitochondrial manganese-dependent superoxide dismutase (SOD2), catalase (CAT), glutathione peroxidase (GPX), and glutathione reductase (GR), and suppressed the expression of matrix metalloproteinases (MMPs) through the mitogen-activated protein kinase (MAPK) signaling pathways, such as c-Jun N-terminal kinase (JNK) and p38. Bioactive compounds analyses were performed using a high-performance liquid chromatography-photodiode array detector (HPLC-PDA) system. The antioxidant activity of Ulmus macrocarpa Hance (UMH) extracts was estimated in vitro. The anti-aging activity of UMH extracts was estimated in vivo using the SKH-1 hairless mice. The UMH extracts reduced the H(2)O(2)-induced intracellular ROS production and the cell damages in human dermal fibroblasts (HDFs). Moreover, the H(2)O(2)-induced phosphorylation of JNK and p38 was detected in HDF and UMH extracts blocked the phosphorylation. These results suggest that UMH extracts can reduce the expression of MMPs and the reduced MMPs lead to the inhibition of collagen degradation. In addition, oral administration of the UMH extracts decreased the depth, thickness, and length of wrinkles on UVB exposed hairless mice. Therefore, UMH extracts play an advantage of the functional materials in antioxidant and anti-aging of skin. MDPI 2017-06-05 /pmc/articles/PMC5486023/ /pubmed/28587261 http://dx.doi.org/10.3390/ijms18061200 Text en © 2017 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Choi, Sun-Il
Lee, Jin-Ha
Kim, Jae-Min
Jung, Tae-Dong
Cho, Bong-Yeon
Choi, Seung-Hyun
Lee, Dae-Won
Kim, Jinkyung
Kim, Jong-Yea
Lee, Ok-Hawn
Ulmus macrocarpa Hance Extracts Attenuated H(2)O(2) and UVB-Induced Skin Photo-Aging by Activating Antioxidant Enzymes and Inhibiting MAPK Pathways
title Ulmus macrocarpa Hance Extracts Attenuated H(2)O(2) and UVB-Induced Skin Photo-Aging by Activating Antioxidant Enzymes and Inhibiting MAPK Pathways
title_full Ulmus macrocarpa Hance Extracts Attenuated H(2)O(2) and UVB-Induced Skin Photo-Aging by Activating Antioxidant Enzymes and Inhibiting MAPK Pathways
title_fullStr Ulmus macrocarpa Hance Extracts Attenuated H(2)O(2) and UVB-Induced Skin Photo-Aging by Activating Antioxidant Enzymes and Inhibiting MAPK Pathways
title_full_unstemmed Ulmus macrocarpa Hance Extracts Attenuated H(2)O(2) and UVB-Induced Skin Photo-Aging by Activating Antioxidant Enzymes and Inhibiting MAPK Pathways
title_short Ulmus macrocarpa Hance Extracts Attenuated H(2)O(2) and UVB-Induced Skin Photo-Aging by Activating Antioxidant Enzymes and Inhibiting MAPK Pathways
title_sort ulmus macrocarpa hance extracts attenuated h(2)o(2) and uvb-induced skin photo-aging by activating antioxidant enzymes and inhibiting mapk pathways
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5486023/
https://www.ncbi.nlm.nih.gov/pubmed/28587261
http://dx.doi.org/10.3390/ijms18061200
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