Cranberry extract attenuates hepatic inflammation in high-fat-fed obese mice

被引:29
|
作者
Glisan, Shannon L. [1 ]
Ryan, Caroline [2 ]
Neilson, Andrew P. [2 ]
Lambert, Joshua D. [1 ,3 ]
机构
[1] Penn State Univ, Dept Food Sci, 332 Rodney A Erickson Food Sci Bldg, University Pk, PA 16802 USA
[2] Virginia Polytech Inst & State Univ, Dept Food Sci & Technol, Blacksburg, VA 24060 USA
[3] Penn State Univ, Ctr Mol Toxicol & Carcinogenesis, University Pk, PA 16802 USA
来源
基金
美国农业部; 美国国家卫生研究院;
关键词
Vaccinium macrocarpon; Cranberry; Nonalcoholic fatty liver disease; Inflammation; Polyphenols; DIET-INDUCED OBESITY; LIVER-DISEASE; METABOLIC ENDOTOXEMIA; UNCOUPLING PROTEIN-2; COCOA PROCYANIDINS; INSULIN-RESISTANCE; GUT MICROBIOTA; CUTTING EDGE; CELLS; STEATOHEPATITIS;
D O I
10.1016/j.jnutbio.2016.07.009
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
Cranberry (Vaccinium macrocarpon) consumption has been associated with health beneficial effects. Nonalcoholic fatty liver disease (NAFLD) is a comorbidity of obesity. In the present study, we investigated the effect of a polyphenol-rich cranberry extract (CBE) on hepatic inflammation in high fat (HF)-fed obese C57BL/6J mice. Following dietary treatment with 0.8% CBE for 10 weeks, we observed no change in body weight or visceral fat mass in CBE-supplemented mice compared to HF-fed control mice. We did observe a significant decrease in plasma alanine aminotransferase (31%) and histological severity of NAFLD (33% decrease in area of involvement, 29% decrease in lipid droplet size) compared to HF-fed controls. Hepatic protein levels of tumor necrosis factor alpha and C-C chemokine ligand 2 were reduced by 28% and 19%, respectively, following CBE supplementation. CBE significantly decreased hepatic mRNA levels of toll-like receptor 4 (TLR4, 63%) and nuclear factor kappa B (NF kappa B, 24%), as well as a number of genes related to the nucleotide-binding domain, leucine-rich-containing family, pyrin domain-containing 3 inflammasome. In conclusion, CBE reduced NAFLD and hepatic inflammation in HF-fed obese C57BL/6J mice. These effects appear to be related to mitigation of TLR4-NF kappa B related signaling; however, further studies into the underlying mechanisms of these hepatoprotective effects are needed. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:60 / 66
页数:7
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