Oral arginine supplementation protects female mice from the onset of non-alcoholic steatohepatitis

被引:41
作者
Sellmann, Cathrin [1 ]
Degen, Christian [1 ]
Jin, Cheng Jun [1 ]
Nier, Anika [2 ]
Engstler, Anna Janina [1 ]
Alkhatib, Dana Hasan [3 ]
De Bandt, Jean-Pascal [4 ,5 ]
Bergheim, Ina [1 ,2 ]
机构
[1] Friedrich Schiller Univ Jena, Inst Nutr Sci, SD Model Syst Mol Nutr, Jena, Germany
[2] Univ Vienna, Dept Nutr Sci, Mol Nutr Sci, Althanstr 14 UZA 2, A-1090 Vienna, Austria
[3] United Arab Emirates Univ, Fac Food & Agr, Nutr & Hlth Dept, Abu Dhabi, U Arab Emirates
[4] Hop Univ Paris Ctr, AP HP, Sorbonne Paris Cite, EA4466, Paris, France
[5] Hop Univ Paris Ctr, AP HP, Dept Clin Chem, Paris, France
关键词
Arginine; Hepatic inflammation; Intestinal barrier function; Lipogenesis; Non-alcoholic steatohepatitis; FATTY LIVER-DISEASE; INTESTINAL BARRIER FUNCTION; NITRIC-OXIDE SYNTHASE; SKELETAL-MUSCLE; ADIPOSE-TISSUE; DIET; PERMEABILITY; METABOLISM; RATS; EXPRESSION;
D O I
10.1007/s00726-017-2423-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Dietary arginine (Arg) supplementation has been proposed to have positive effects on the development of liver diseases. In the present study, we investigate if an oral Arg supplementation in diet protects mice fed a fructose, fat and cholesterol enriched Western-style diet (WSD) from the development of non-alcoholic steatohepatitis (NASH). Female C57BL/6J mice were fed a liquid control diet or a liquid WSD +/- Arg (2.49 g/kg body weight/day) for 6 weeks. Indices of liver injury, glucose metabolism and intestinal permeability were determined. While Arg supplementation had no effects on body weight gain, fasting blood glucose levels were significantly lower in WSD+Arg-fed mice than in C+Arg-fed animals. WSD-fed mice developed liver steatosis accompanied with inflammation, both being significantly attenuated in WSD+Arg-fed mice. These effects of Arg supplementation went along with a protection against WSD-induced decreased tight junction protein levels in the upper parts of the small intestine, increased levels of bacterial endotoxin in portal plasma as well as increased hepatic toll-like receptor-4 mRNA and 4-hydroxynonenal protein adduct levels. In conclusion, Arg supplementation may protect mice from the development of NASH.
引用
收藏
页码:1215 / 1225
页数:11
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