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结肠咖啡酚代谢物、二羟咖啡酸、二羟阿魏酸和对羟基苯乙酸可保护肝细胞免受 TNF-α 诱导的炎症和氧化应激。

Colonic Coffee Phenols Metabolites, Dihydrocaffeic, Dihydroferulic, and Hydroxyhippuric Acids Protect Hepatic Cells from TNF-α-Induced Inflammation and Oxidative Stress.

机构信息

Department of Metabolism and Nutrition, Institute of Food Science, Technology and Nutrition (ICTAN-CSIC), Spanish National Research Council (CSIC), José Antonio Nováis 10, 28040 Madrid, Spain.

Department of Nutrition and Food Science, Faculty of Pharmacy, Universidad Complutense de Madrid (UCM), Plaza de Ramón y Cajal, s/n, 28040 Madrid, Spain.

出版信息

Int J Mol Sci. 2023 Jan 11;24(2):1440. doi: 10.3390/ijms24021440.

DOI:10.3390/ijms24021440
PMID:36674952
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9863622/
Abstract

Coffee presents beneficial health properties, including antiobesity effects. However, its effects on inflammation are controversial. Hydroxycinnamic acids are the main coffee phenolic bioactive compounds. In human bioavailability studies carried out with coffee, among the most abundant compounds found in urine and plasma were the colonic metabolites, dihydrocaffeic (DHCA), dihydroferulic (DHFA), and hydroxyhippuric (HHA) acids. To understand the hepato-protective potential of these three compounds, we tested whether treatment with realistic concentrations (0.5-10 µM) were effective to counteract inflammatory process and oxidative status induced by tumor necrosis factor α (TNF-α). First, we established a novel model of inflammation/oxidation using TNF-α and HepG2 cells. Afterwards, we evaluated the activity of DHCA, DHFA, and HHA against the inflammatory/oxidative challenge through the determination of the inflammatory mediators, interleukins (IL)-6, and IL-8 and chemokines, monocyte chemoattractant protein-1, and macrophage inflammatory protein-1, as well as the levels of biomarkers of oxidative stress, such as reactive oxygen species, reduced glutathione, and the antioxidant enzymes glutathione peroxidase and reductase. Results showed that all three compounds have a potential hepato-protective effect against the induced inflammatory/oxidative insult.

摘要

咖啡具有有益的健康特性,包括抗肥胖作用。然而,其对炎症的影响存在争议。羟基肉桂酸是咖啡中主要的酚类生物活性化合物。在对咖啡进行的人体生物利用度研究中,在尿液和血浆中发现的最丰富的化合物是结肠代谢物二羟咖啡酸(DHCA)、二羟阿魏酸(DHFA)和羟基马尿酸(HHA)。为了了解这三种化合物的保肝潜力,我们测试了用现实浓度(0.5-10 μM)治疗是否能有效对抗肿瘤坏死因子 α(TNF-α)诱导的炎症过程和氧化应激。首先,我们使用 TNF-α和 HepG2 细胞建立了一种新的炎症/氧化模型。然后,我们通过测定炎症介质白细胞介素(IL)-6 和 IL-8 以及趋化因子单核细胞趋化蛋白-1 和巨噬细胞炎症蛋白-1,以及氧化应激生物标志物如活性氧、还原型谷胱甘肽和抗氧化酶谷胱甘肽过氧化物酶和还原酶,评估了 DHCA、DHFA 和 HHA 对炎症/氧化应激的活性。结果表明,这三种化合物都具有潜在的保肝作用,可对抗诱导的炎症/氧化损伤。

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