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Fermentation of Panax notoginseng root extract polysaccharides attenuates oxidative stress and promotes type I procollagen synthesis in human dermal fibroblast cells

BACKGROUND: Panax notoginseng is one of the most valuable traditional Chinese medicines. Polysaccharides in P. notoginseng has been shown to significantly reduce the incidence of human diseases. However the application of fermentation technology in Panax notoginseng is not common, and the mechanism...

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Autores principales: You, Shiquan, Shi, Xiuqin, Yu, Dan, Zhao, Dan, An, Quan, Wang, Dongdong, Zhang, Jiachan, Li, Meng, Wang, Changtao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7807718/
https://www.ncbi.nlm.nih.gov/pubmed/33446178
http://dx.doi.org/10.1186/s12906-020-03197-8
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author You, Shiquan
Shi, Xiuqin
Yu, Dan
Zhao, Dan
An, Quan
Wang, Dongdong
Zhang, Jiachan
Li, Meng
Wang, Changtao
author_facet You, Shiquan
Shi, Xiuqin
Yu, Dan
Zhao, Dan
An, Quan
Wang, Dongdong
Zhang, Jiachan
Li, Meng
Wang, Changtao
author_sort You, Shiquan
collection PubMed
description BACKGROUND: Panax notoginseng is one of the most valuable traditional Chinese medicines. Polysaccharides in P. notoginseng has been shown to significantly reduce the incidence of human diseases. However the application of fermentation technology in Panax notoginseng is not common, and the mechanism of action of P. notoginseng polysaccharides produced by fermentation is still unclear. The specific biological mechanisms of fermented P. notoginseng polysaccharides (FPNP) suppresses H(2)O(2)-induced apoptosis in human dermal fibroblast (HDF) and the underlying mechanism are not well understood. METHODS: In this study, the effects of water extracted and fermentation on concentration of polysaccharides in P. notoginseng extracts were analyzed. After the H(2)O(2)-induced HDF model of oxidative damage was established, and then discussed by the expression of cell markers, including ROS, MDA, SOD, CAT, GSH-Px and MMP-1, COL-I, ELN, which were detected by related ELISA kits. The expression of TGF-β/Smad pathway markers were tested by qRT-PCR to determine whether FPNP exerted antioxidant activity through TGF-β signaling in HDF cells. RESULTS: The polysaccharide content of Panax notoginseng increased after Saccharomyces cerevisiae CGMCC 17452 fermentation. In the FPNP treatment group, ROS and MDA contents were decreased, reversed the down-regulation of the antioxidant activity and expression of antioxidant enzyme (CAT, GSH-Px and SOD) induced by H(2)O(2). Furthermore, the up-regulation in expression of TGF-β, Smad2/3 and the down-regulation in the expression of Smad7 in FPNP treated groups revealed that FPNP can inhibit H(2)O(2)-induced collagen and elastin injury by activating TGF-β/Smad signaling pathway. CONCLUSION: It was shown that FPNP could inhibit the damage of collagen and elastin induced by H(2)O(2) by activating the TGF-β/Smad signaling pathway, thereby protecting against the oxidative damage induced by hydrogen peroxide. FPNP may be an effective attenuating healing agent that protects the skin from oxidative stress and wrinkles.
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spelling pubmed-78077182021-01-15 Fermentation of Panax notoginseng root extract polysaccharides attenuates oxidative stress and promotes type I procollagen synthesis in human dermal fibroblast cells You, Shiquan Shi, Xiuqin Yu, Dan Zhao, Dan An, Quan Wang, Dongdong Zhang, Jiachan Li, Meng Wang, Changtao BMC Complement Med Ther Research Article BACKGROUND: Panax notoginseng is one of the most valuable traditional Chinese medicines. Polysaccharides in P. notoginseng has been shown to significantly reduce the incidence of human diseases. However the application of fermentation technology in Panax notoginseng is not common, and the mechanism of action of P. notoginseng polysaccharides produced by fermentation is still unclear. The specific biological mechanisms of fermented P. notoginseng polysaccharides (FPNP) suppresses H(2)O(2)-induced apoptosis in human dermal fibroblast (HDF) and the underlying mechanism are not well understood. METHODS: In this study, the effects of water extracted and fermentation on concentration of polysaccharides in P. notoginseng extracts were analyzed. After the H(2)O(2)-induced HDF model of oxidative damage was established, and then discussed by the expression of cell markers, including ROS, MDA, SOD, CAT, GSH-Px and MMP-1, COL-I, ELN, which were detected by related ELISA kits. The expression of TGF-β/Smad pathway markers were tested by qRT-PCR to determine whether FPNP exerted antioxidant activity through TGF-β signaling in HDF cells. RESULTS: The polysaccharide content of Panax notoginseng increased after Saccharomyces cerevisiae CGMCC 17452 fermentation. In the FPNP treatment group, ROS and MDA contents were decreased, reversed the down-regulation of the antioxidant activity and expression of antioxidant enzyme (CAT, GSH-Px and SOD) induced by H(2)O(2). Furthermore, the up-regulation in expression of TGF-β, Smad2/3 and the down-regulation in the expression of Smad7 in FPNP treated groups revealed that FPNP can inhibit H(2)O(2)-induced collagen and elastin injury by activating TGF-β/Smad signaling pathway. CONCLUSION: It was shown that FPNP could inhibit the damage of collagen and elastin induced by H(2)O(2) by activating the TGF-β/Smad signaling pathway, thereby protecting against the oxidative damage induced by hydrogen peroxide. FPNP may be an effective attenuating healing agent that protects the skin from oxidative stress and wrinkles. BioMed Central 2021-01-14 /pmc/articles/PMC7807718/ /pubmed/33446178 http://dx.doi.org/10.1186/s12906-020-03197-8 Text en © The Author(s) 2021 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
You, Shiquan
Shi, Xiuqin
Yu, Dan
Zhao, Dan
An, Quan
Wang, Dongdong
Zhang, Jiachan
Li, Meng
Wang, Changtao
Fermentation of Panax notoginseng root extract polysaccharides attenuates oxidative stress and promotes type I procollagen synthesis in human dermal fibroblast cells
title Fermentation of Panax notoginseng root extract polysaccharides attenuates oxidative stress and promotes type I procollagen synthesis in human dermal fibroblast cells
title_full Fermentation of Panax notoginseng root extract polysaccharides attenuates oxidative stress and promotes type I procollagen synthesis in human dermal fibroblast cells
title_fullStr Fermentation of Panax notoginseng root extract polysaccharides attenuates oxidative stress and promotes type I procollagen synthesis in human dermal fibroblast cells
title_full_unstemmed Fermentation of Panax notoginseng root extract polysaccharides attenuates oxidative stress and promotes type I procollagen synthesis in human dermal fibroblast cells
title_short Fermentation of Panax notoginseng root extract polysaccharides attenuates oxidative stress and promotes type I procollagen synthesis in human dermal fibroblast cells
title_sort fermentation of panax notoginseng root extract polysaccharides attenuates oxidative stress and promotes type i procollagen synthesis in human dermal fibroblast cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7807718/
https://www.ncbi.nlm.nih.gov/pubmed/33446178
http://dx.doi.org/10.1186/s12906-020-03197-8
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