(-)-Epigallocatechin-3-gallate decreases colonic inflammation and permeability in a mouse model of colitis, but reduces macronutrient digestion and exacerbates weight loss

被引:83
作者
Bitzer, Zachary T. [1 ]
Elias, Ryan J. [1 ]
Vijay-Kumar, Matam [2 ]
Lambert, Joshua D. [1 ,3 ]
机构
[1] Penn State Univ, Dept Food Sci, University Pk, PA 16802 USA
[2] Penn State Univ, Dept Nutr Sci, University Pk, PA 16802 USA
[3] Penn State Univ, Ctr Mol Toxicol & Carcinogenesis, University Pk, PA 16802 USA
基金
美国国家卫生研究院;
关键词
Antinutritional effects; (-)-Epigallocatechin-3-gallate; Gastrointestinal permeability; Green tea; Intestinal inflammation; GREEN TEA POLYPHENOLS; GUT-PERMEABILITY; EPIGALLOCATECHIN GALLATE; MICE; INHIBITION; METABOLISM; MICROBIOTA; SUCRALOSE; TOXICITY; DISEASE;
D O I
10.1002/mnfr.201501042
中图分类号
TS2 [食品工业];
学科分类号
100403 [营养与食品卫生学];
摘要
Scope: (-)-Epigallocatechin-3-gallate (EGCG) has been reported to have putative health effects including the prevention of inflammation and obesity. Historically, polyphenols have been regarded as antinutritionals and while such effects may be beneficial in obese subjects, they may be deleterious in nutritionally compromised individuals. Methods and results: We examined the effect of EGCG in the dextran sulfate sodium (DSS)-treated mouse model of ulcerative colitis. Following induction of colitis, mice were treated with EGCG (3.2 mg/g) as the sole source of drinking fluid for 3 days. EGCG treatment mitigated DSS-induced colon shortening and spleen enlargement. EGCG also decreased colonic protein levels of IL-1 beta, IL-6, and tumor necrosis factor-alpha, as well as colonic lipid peroxides compared to DSS-treated controls. We observed that EGCG reduced DSS-induced gastrointestinal permeability. These beneficial effects were offset by enhanced body weight loss in EGCG-treated mice compared to DSS-treated controls. These effects were related to decreased protein and lipid digestion in EGCG-treated mice compared to DSS-treated controls. Conclusions: Our results suggest that although EGCG may exert anti-inflammatory effects, its ability to modulate macronutrient digestion may represent a dose-limiting adverse effect that must be considered in the context of its use for treating inflammatory bowel disease.
引用
收藏
页码:2267 / 2274
页数:8
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