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原花青素和根皮苷对人 THP-1 巨噬细胞免疫调节活性的代谢组学研究

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

机构信息

Department of Analytical and Food Chemistry, Facultade de Ciencias, Universidade de Vigo, Campus da Auga, 32004 Ourense, Spain.

Department of Chemistry and Biochemistry, Faculty of Sciences, LAQV/REQUIMTE, University of Porto, E-4169-007 Porto, Portugal.

出版信息

Molecules. 2021 Feb 3;26(4):787. doi: 10.3390/molecules26040787.

Abstract

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.

摘要

二氢查尔酮、根皮苷(PZ)及其苷元根皮素(PT)通过多种机制显示出免疫调节作用。然而,导致这些特性的差异代谢特征在很大程度上尚不清楚。由于巨噬细胞在免疫反应中起着重要作用,我们的研究旨在描述 PZ 和 PT 暴露下的人 THP-1 巨噬细胞。首次使用基于多平台的非靶向代谢组学方法来揭示与二氢查尔酮在 LPS 刺激的巨噬细胞中触发的抗炎机制相关的代谢物。结果表明,所有处理均导致巨噬细胞表现出不同的表型反应。二氢查尔酮处理 LPS 刺激的巨噬细胞模拟了正常条件下的反应,表明抑制了 LPS 反应。除了促进氨基酸生物合成外,二氢查尔酮对 LPS 的拮抗作用主要表现在甘油磷脂和鞘脂代谢中。此外,PT 比 PZ 表现出更大的代谢活性。总的来说,这项研究的结果提供了关于 PZ 和 PT 在调节人类细胞炎症反应的作用机制的代谢水平的知识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ea1/7913540/f1e90201b6be/molecules-26-00787-g001.jpg

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