Structural Characterization and Antifatigue Activity of a Novel Exopolysaccharide Isolated from Marasmius androsaceus

被引:0
作者
Du, Peng [1 ]
Li, Nan [1 ,2 ]
Wang, Junqing [1 ]
Li, Piwu [1 ]
Song, Jia [2 ]
Geng, Xiaoqi [3 ]
Zhang, Ziyang [1 ]
Yang, Shuai [4 ]
Wang, Ruiming [1 ]
机构
[1] Qilu Univ Technol, State Key Lab Biobased Mat & Green Papermaking LBM, Jinan 250353, Shandong, Peoples R China
[2] Tianjin Univ Sci & Technol, Key Lab Ind Fermentat Microbiol, Minist Educ, Tianjin 300457, Peoples R China
[3] Dongxiao Bioengn Shandong Co Ltd, Jinan 250000, Shandong, Peoples R China
[4] Beijing Boxbio Sci & Technol Co Ltd, Beijing 101100, Peoples R China
关键词
ANTI-FATIGUE ACTIVITY; WATER-SOLUBLE POLYSACCHARIDES; IMMUNOMODULATORY ACTIVITY; FERMENTATION; PURIFICATION; ANTIOXIDANT; HEMICELLULOSES; FRACTIONS; PROPERTY;
D O I
10.1155/2023/2180179
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This study aimed at examining the structure-role modeling and antifatigue mechanism of polysaccharides, including M. androsaceus exopolysaccharide 3 (MEPS3), isolated from Marasmius androsaceus fermentation broth. The molecular weight of MEPS3 was 10.47 kDa. Furthermore, monosaccharide analysis showed the presence of mannose, glucose, and galactose in MEPS3 in a molar ratio of 0.08: 0.34 :1.46. Mannose, a-galactose, and a-d-glucose anomeric hydrogen signals were detected using nuclear magnetic resonance spectroscopy. MEPS3 was found to contain glyoxylic acid, forming rod-like chains that support high-purity polymerization. The weight-loaded swimming test results showed that MEPS3 treatment reduced lactic acid (LA) levels by 25.72% and increased the lactate dehydrogenase (LDH) activity by 5.67% in the plasma. Furthermore, it lowered malondialdehyde (MDA) levels by 47.09% and increased reactive oxygen species (ROS) and glutathione peroxidase (GSH-Px) levels by 52.42 and 97.03%, respectively, in the plasma. In addition, MEPS3 treatment reduced MDA and ROS levels in the liver by 28.85 and 18.64% while increasing superoxide dismutase (SOD) and GSH-Px levels by 17.41 and 38.13%, respectively. MEPS3 treatment increased the expression of nuclear factor-erythroid 2-related factor 2, glutamate-cysteine ligase, quinone oxidoreductase 1, and heme oxygenase 1 by 22.5, 24.8, 20.3, and 43.1%, respectively, in the liver. These findings demonstrate that MEPS3 efectively alleviates fatigue by removing harmful metabolites and indicate that the antifatigue mechanism is related to the Nrf-2 signaling pathway.
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页数:15
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