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Antioxidant Activity of Gracilaria lemaneiformis Polysaccharide Degradation Based on Nrf-2/Keap-1 Signaling Pathway in HepG2 Cells with Oxidative Stress Induced by H(2)O(2)

The objective of this research was to investigate the antioxidant activity of Gracilaria lemaneiformis polysaccharide degradation and its underlying mechanism involved in the Nrf-2/Keap-1 signaling pathway in HepG2 cells with oxidative stress induced by H(2)O(2). The result of the scavenging ability...

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Autores principales: Long, Xiaoshan, Hu, Xiao, Pan, Chuang, Xiang, Huan, Chen, Shengjun, Qi, Bo, Liu, Shucheng, Yang, Xianqing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9506308/
https://www.ncbi.nlm.nih.gov/pubmed/36135734
http://dx.doi.org/10.3390/md20090545
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author Long, Xiaoshan
Hu, Xiao
Pan, Chuang
Xiang, Huan
Chen, Shengjun
Qi, Bo
Liu, Shucheng
Yang, Xianqing
author_facet Long, Xiaoshan
Hu, Xiao
Pan, Chuang
Xiang, Huan
Chen, Shengjun
Qi, Bo
Liu, Shucheng
Yang, Xianqing
author_sort Long, Xiaoshan
collection PubMed
description The objective of this research was to investigate the antioxidant activity of Gracilaria lemaneiformis polysaccharide degradation and its underlying mechanism involved in the Nrf-2/Keap-1 signaling pathway in HepG2 cells with oxidative stress induced by H(2)O(2). The result of the scavenging ability of free radicals showed that GLP-HV (polysaccharide degraded by H(2)O(2)–vitamin C (Vc)) performed a better scavenging ability than GLP (G. lemaneiformis polysaccharide). Moreover, the scavenging ability of polysaccharide to these free radicals from strong to weak was as follows: superoxide radical, ferric ion, ABTS(+), and DPPH radical, and their IC(50) values were 3.56 ± 0.0028, 4.97 ± 0.18, 9.62 ± 0.35, and 23.85 ± 1.78 mg/mL, respectively. Furthermore, GLP-HV obviously relieved oxidative stress in HepG2 cells, which strengthened the activity of T-AOC, CAT, GSH-PX, and SOD, and diminished the intensity of MDA, intracellular ROS, and calcium ion based on the Nrf-2/Keap-1 signaling pathway. The PCR result revealed that polysaccharide upregulated the expression of the genes Nrf-2, HO-1, NQO-1, and ZO-1 and downregulated Keap-1. The correlation between chemical properties and antioxidant mechanism of GLP-HV was evaluated via a heat map. The results illustrated that reducing sugar and active groups presented a positive correlation, and molecular weight and viscosity exhibited a negative relation with antioxidant activity.
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spelling pubmed-95063082022-09-24 Antioxidant Activity of Gracilaria lemaneiformis Polysaccharide Degradation Based on Nrf-2/Keap-1 Signaling Pathway in HepG2 Cells with Oxidative Stress Induced by H(2)O(2) Long, Xiaoshan Hu, Xiao Pan, Chuang Xiang, Huan Chen, Shengjun Qi, Bo Liu, Shucheng Yang, Xianqing Mar Drugs Article The objective of this research was to investigate the antioxidant activity of Gracilaria lemaneiformis polysaccharide degradation and its underlying mechanism involved in the Nrf-2/Keap-1 signaling pathway in HepG2 cells with oxidative stress induced by H(2)O(2). The result of the scavenging ability of free radicals showed that GLP-HV (polysaccharide degraded by H(2)O(2)–vitamin C (Vc)) performed a better scavenging ability than GLP (G. lemaneiformis polysaccharide). Moreover, the scavenging ability of polysaccharide to these free radicals from strong to weak was as follows: superoxide radical, ferric ion, ABTS(+), and DPPH radical, and their IC(50) values were 3.56 ± 0.0028, 4.97 ± 0.18, 9.62 ± 0.35, and 23.85 ± 1.78 mg/mL, respectively. Furthermore, GLP-HV obviously relieved oxidative stress in HepG2 cells, which strengthened the activity of T-AOC, CAT, GSH-PX, and SOD, and diminished the intensity of MDA, intracellular ROS, and calcium ion based on the Nrf-2/Keap-1 signaling pathway. The PCR result revealed that polysaccharide upregulated the expression of the genes Nrf-2, HO-1, NQO-1, and ZO-1 and downregulated Keap-1. The correlation between chemical properties and antioxidant mechanism of GLP-HV was evaluated via a heat map. The results illustrated that reducing sugar and active groups presented a positive correlation, and molecular weight and viscosity exhibited a negative relation with antioxidant activity. MDPI 2022-08-24 /pmc/articles/PMC9506308/ /pubmed/36135734 http://dx.doi.org/10.3390/md20090545 Text en © 2022 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
Long, Xiaoshan
Hu, Xiao
Pan, Chuang
Xiang, Huan
Chen, Shengjun
Qi, Bo
Liu, Shucheng
Yang, Xianqing
Antioxidant Activity of Gracilaria lemaneiformis Polysaccharide Degradation Based on Nrf-2/Keap-1 Signaling Pathway in HepG2 Cells with Oxidative Stress Induced by H(2)O(2)
title Antioxidant Activity of Gracilaria lemaneiformis Polysaccharide Degradation Based on Nrf-2/Keap-1 Signaling Pathway in HepG2 Cells with Oxidative Stress Induced by H(2)O(2)
title_full Antioxidant Activity of Gracilaria lemaneiformis Polysaccharide Degradation Based on Nrf-2/Keap-1 Signaling Pathway in HepG2 Cells with Oxidative Stress Induced by H(2)O(2)
title_fullStr Antioxidant Activity of Gracilaria lemaneiformis Polysaccharide Degradation Based on Nrf-2/Keap-1 Signaling Pathway in HepG2 Cells with Oxidative Stress Induced by H(2)O(2)
title_full_unstemmed Antioxidant Activity of Gracilaria lemaneiformis Polysaccharide Degradation Based on Nrf-2/Keap-1 Signaling Pathway in HepG2 Cells with Oxidative Stress Induced by H(2)O(2)
title_short Antioxidant Activity of Gracilaria lemaneiformis Polysaccharide Degradation Based on Nrf-2/Keap-1 Signaling Pathway in HepG2 Cells with Oxidative Stress Induced by H(2)O(2)
title_sort antioxidant activity of gracilaria lemaneiformis polysaccharide degradation based on nrf-2/keap-1 signaling pathway in hepg2 cells with oxidative stress induced by h(2)o(2)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9506308/
https://www.ncbi.nlm.nih.gov/pubmed/36135734
http://dx.doi.org/10.3390/md20090545
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