Metabolomics Insights of the Immunomodulatory Activities of Phlorizin and Phloretin on Human THP-1 Macrophages

被引:6
|
作者
Cambeiro-Perez, Noelia [1 ]
Gonzalez-Gomez, Xiana [1 ]
Gonzalez-Barreiro, Carmen [1 ]
Rosa Perez-Gregorio, Maria [2 ]
Fernandes, Iva [2 ]
Mateus, Nuno [2 ]
de Freitas, Victor [2 ]
Sanchez, Borja [3 ]
Martinez-Carballo, Elena [1 ]
机构
[1] Univ Vigo, Fac Ciencias, Dept Analyt & Food Chem, Campus Auga, Orense 32004, Spain
[2] Univ Porto, Fac Sci, Dept Chem & Biochem, LAQV REQUIMTE, E-4169007 Porto, Portugal
[3] Spanish Natl Res Council IPLA CSIC, Dairy Res Inst Asturias, Dept Microbiol & Biochem, Paseo Rio Linares Sn, Villaviciosa 33300, Spain
来源
MOLECULES | 2021年 / 26卷 / 04期
关键词
untargeted metabolomics; THP-1; macrophages; phloretin; phlorizin; immunomodulation;
D O I
10.3390/molecules26040787
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
Dihydrochalcones, phlorizin (PZ) and its aglycone phloretin (PT), have evidenced immunomodulatory effects through several mechanisms. However, the differential metabolic signatures that lead to these properties are largely unknown. Since macrophages play an important role in the immune response, our study aimed to characterise human THP-1 macrophages under PZ and PT exposure. A multiplatform-based untargeted metabolomics approach was used to reveal metabolites associated with the anti-inflammatory mechanisms triggered by the dihydrochalcones in LPS-stimulated macrophages, for the first time. Results showed differential phenotypic response in macrophages for all treatments. Dihydrochalcone treatment in LPS-stimulated macrophages mimics the response under normal conditions, suggesting inhibition of LPS response. Antagonistic effects of dihydrochalcones against LPS was mainly observed in glycerophospholipid and sphingolipid metabolism besides promoting amino acid biosynthesis. Moreover, PT showed greater metabolic activity than PZ. Overall, the findings of this study yielded knowledge about the mechanisms of action PZ and PT at metabolic level in modulating inflammatory response in human cells.
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页数:13
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