共 43 条
Xanthohumol, a chalcon derived from hops, inhibits hepatic inflammation and fibrosis
被引:85
作者:

Dorn, Christoph
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机构:
Univ Hosp Regensburg, Dept Internal Med 1, D-93042 Regensburg, Germany Univ Hosp Regensburg, Dept Internal Med 1, D-93042 Regensburg, Germany

Kraus, Birgit
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Univ Regensburg, Inst Pharm, D-8400 Regensburg, Germany Univ Hosp Regensburg, Dept Internal Med 1, D-93042 Regensburg, Germany

Motyl, Magdalena
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Univ Regensburg, Inst Pharm, D-8400 Regensburg, Germany Univ Hosp Regensburg, Dept Internal Med 1, D-93042 Regensburg, Germany

Weiss, Thomas S.
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h-index: 0
机构:
Univ Hosp Regensburg, Dept Surg, Ctr Liver Cell Res, D-93042 Regensburg, Germany Univ Hosp Regensburg, Dept Internal Med 1, D-93042 Regensburg, Germany

Gehrig, Manfred
论文数: 0 引用数: 0
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机构:
Nateco, Wolnzach, Germany Univ Hosp Regensburg, Dept Internal Med 1, D-93042 Regensburg, Germany

Schoelmerich, Juergen
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机构:
Univ Hosp Regensburg, Dept Internal Med 1, D-93042 Regensburg, Germany Univ Hosp Regensburg, Dept Internal Med 1, D-93042 Regensburg, Germany

Heilmann, Joerg
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机构:
Univ Regensburg, Inst Pharm, D-8400 Regensburg, Germany Univ Hosp Regensburg, Dept Internal Med 1, D-93042 Regensburg, Germany

Hellerbrand, Claus
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h-index: 0
机构:
Univ Hosp Regensburg, Dept Internal Med 1, D-93042 Regensburg, Germany Univ Hosp Regensburg, Dept Internal Med 1, D-93042 Regensburg, Germany
机构:
[1] Univ Hosp Regensburg, Dept Internal Med 1, D-93042 Regensburg, Germany
[2] Univ Regensburg, Inst Pharm, D-8400 Regensburg, Germany
[3] Univ Hosp Regensburg, Dept Surg, Ctr Liver Cell Res, D-93042 Regensburg, Germany
[4] Nateco, Wolnzach, Germany
关键词:
Chalcon;
Fibrosis;
NASH;
Steatosis;
Xanthohumol;
HUMULUS-LUPULUS L;
FACTOR-KAPPA-B;
NONALCOHOLIC STEATOHEPATITIS;
PRENYLATED FLAVONOIDS;
LIVER STEATOSIS;
CELL APOPTOSIS;
RAT;
EXPRESSION;
ACID;
BEER;
D O I:
10.1002/mnfr.200900314
中图分类号:
TS2 [食品工业];
学科分类号:
0832 ;
摘要:
Xanthohumol (XN) is a major prenylated chalcone found in hops, which is used to add bitterness and flavor to beer. In this study, we first investigated the effects of XN on hepatocytes and hepatic stellate cells (HSC), the central mediators of liver fibrogenesis. XN inhibited the activation of primary human HSC and induced apoptosis in activated HSC in vitro in a dose dependent manner (0-20 mu M). In contrast, XN doses as high as 50 mM did not impair viability of primary human hepatocytes. However, in both cell types XN inhibited activation of the transcription factor NF kappa B and expression of NF kappa B dependent proinflammatory genes. In vivo, feeding of XN reduced hepatic inflammation and expression of profibrogenic genes in a murine model of non-alcoholic steatohepatitis. These data indicate that XN has the potential as functional nutrient for the prevention or treatment of nonalcoholic steatohepatitis or other chronic liver disease.
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收藏
页码:S205 / S213
页数:9
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