4.7 Article

Green Tea Extract Treatment in Obese Mice with Nonalcoholic Steatohepatitis Restores the Hepatic Metabolome in Association with Limiting Endotoxemia-TLR4-NFκB-Mediated Inflammation

Journal

MOLECULAR NUTRITION & FOOD RESEARCH
Volume 63, Issue 24, Pages -

Publisher

WILEY
DOI: 10.1002/mnfr.201900811

Keywords

green tea; gut permeability; metabolic endotoxemia; nonalcoholic steatohepatitis; polar metabolomics

Funding

  1. NCI NIH HHS [P30 CA016058] Funding Source: Medline

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Scope Catechin-rich green tea extract (GTE) alleviates nonalcoholic steatohepatitis (NASH) by lowering endotoxin-TLR4 (Toll-like receptor-4)-NF kappa B (nuclear factor kappa-B) inflammation. This study aimed to define altered MS-metabolomic responses during high-fat (HF)-induced NASH that are restored by GTE utilizing livers from an earlier study in which GTE decreased endotoxin-TLR4-NF kappa B liver injury. Methods and results Mice are fed a low-fat (LF) or HF diet for 12 weeks and then randomized to LF or HF diets containing 0% or 2% GTE for an additional 8 weeks. Global MS-based metabolomics and targeted metabolite profiling of catechins/catechin metabolites are evaluated. GTE in HF mice restores hepatic metabolites implicated in dyslipidemia insulin resistance, and inflammation. These include 122 metabolites: amino acids, lipids, nucleotides, vitamins, bile acids, flavonoids, xenobiotics, and carbohydrates. Hepatic amino acids, B-vitamins, and bile acids are inversely correlated with biomarkers of insulin resistance, liver injury, steatosis, and inflammation. Further, phosphatidylcholine metabolites are positively correlated with biomarkers of liver injury and NF kappa B inflammation. Thirteen catechin metabolites are identified in livers of GTE-treated mice, mostly as phase II conjugates of parental catechins or microbial-derived valerolactones. Conclusion The defined anti-inflammatory/metabolic interactions advance an understanding of the mechanism by which GTE catechins protect against NF kappa B-mediated liver injury in NASH.

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