Colonic Coffee Phenols Metabolites, Dihydrocaffeic, Dihydroferulic, and Hydroxyhippuric Acids Protect Hepatic Cells from TNF-α-Induced Inflammation and Oxidative Stress.
Andrea Sánchez-MedinaMónica Redondo-PuenteRudolf DupakLaura Bravo-ClementeLuis GoyaBeatriz SarriáPublished in: International journal of molecular sciences (2023)
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.
Keyphrases
- oxidative stress
- diabetic rats
- rheumatoid arthritis
- ischemia reperfusion injury
- dna damage
- induced apoptosis
- endothelial cells
- reactive oxygen species
- healthcare
- high glucose
- human health
- mental health
- dendritic cells
- health information
- risk assessment
- drug induced
- small molecule
- nitric oxide
- induced pluripotent stem cells
- solid phase extraction
- molecularly imprinted
- heat stress
- replacement therapy