Hypnea musciformis Seaweed Extract Protected Human Mesenchymal Stem Cells From Oxidative Stress Through NRF2 Activation

被引:0
作者
Goutas, Andreas [1 ,2 ]
Goutzourelas, Nikolaos [1 ]
Kevrekidou, Alkistis [3 ,4 ]
Kevrekidis, Dimitrios Phaedon [5 ]
Malea, Paraskevi [6 ]
Virgiliou, Christina [7 ]
Assimopoulou, Andreana N. [3 ]
Trachana, Varvara [2 ]
Kollatos, Nikolaos [1 ]
Moustafa, Tafa [1 ]
Liu, Ming [8 ,9 ]
Lin, Xiukun [10 ]
Komiotis, Dimitrios [1 ]
Stagos, Dimitrios [1 ]
机构
[1] Univ Thessaly, Sch Hlth Sci, Dept Biochem & Biotechnol, Larisa, Greece
[2] Univ Thessaly, Fac Med, Dept Biol, Larisa, Greece
[3] Aristotle Univ Thessaloniki, Sch Chem Engn, Lab Organ Chem, Thessaloniki, Greece
[4] Aristotle Univ Thessaloniki, Dept Chem Engn, Environm Engn Lab, Thessaloniki, Greece
[5] Aristotle Univ Thessaloniki, Dept Med, Lab Forens Med & Toxicol, Thessaloniki, Greece
[6] Aristotle Univ Thessaloniki, Sch Biol, Dept Bot, Thessaloniki, Greece
[7] Aristotle Univ Thessaloniki, Sch Chem Engn, Lab Analyt Chem, Thessaloniki, Greece
[8] Ocean Univ China, Sch Med & Pharm, Key Lab Marine Drugs, Minist Educ, Qingdao, Peoples R China
[9] Qingdao Natl Lab Marine Sci & Technol, Lab Marine Drugs & Bioprod, Qingdao, Peoples R China
[10] Southwest Med Univ, Sch Pharm, Dept Pharmacol, Luzhou, Peoples R China
关键词
antioxidant; <fixed-case>Hypnea musciformis</fixed-case>; macroalgae; mesenchymal cells; NRF2; seaweeds; LIPID-PEROXIDATION; SULFATED POLYSACCHARIDE; RED SEAWEED; DNA-DAMAGE; ANTIOXIDANT; RHODOPHYTA; ENZYMES; ACID;
D O I
10.1002/fsn3.4615
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Previous studies have shown that Hypnea musciformis seaweed extracts (HMEs) possess antioxidant properties, but the molecular mechanisms accounting for this activity are not known. Thus, the present study investigated the molecular mechanisms through which HME exerted its antioxidant activity in human mesenchymal stem cells (WJ-MSCs). After the isolation of HME, its chemical composition was analyzed with gas chromatography mass spectrometry, indicating that it contained amino acids, organic acids, organic amides, sugar alcohols, saturated fatty acids, hydrogenated diterpene alcohols, and other organic compounds. Afterward, HME was shown in vitro to scavenge DPPH<middle dot>, ABTS<middle dot>+, <middle dot>OH, and O2<middle dot>- radicals, possess reducing activity, and protect from ROO<middle dot>-induced DNA strand breakage. Finally, the results showed that HME treatment of WJ-MSCs prevented H2O2-induced oxidative stress by decreasing lipid peroxidation, protein oxidation, reactive oxygen species levels, and DNA damage and by increasing glutathione levels. Moreover, our findings showed for the first time that HME's antioxidant activity in WJ-MSCs was mediated through the activation of NRF2, which upregulated the expression of the antioxidant proteins GCLC, GSR, HMOX1, SOD1, TXN, and GPX1. These results provide new insights into H. musciformis' antioxidant properties, which could help substantially its use as a food supplement or for developing biofunctional foods.
引用
收藏
页码:10816 / 10835
页数:20
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