Xanthohumol, a chalcon derived from hops, inhibits hepatic inflammation and fibrosis

被引:85
作者
Dorn, Christoph [1 ]
Kraus, Birgit [2 ]
Motyl, Magdalena [2 ]
Weiss, Thomas S. [3 ]
Gehrig, Manfred [4 ]
Schoelmerich, Juergen [1 ]
Heilmann, Joerg [2 ]
Hellerbrand, Claus [1 ]
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.
引用
收藏
页码:S205 / S213
页数:9
相关论文
共 43 条
[1]   Mechanisms of the antiangiogenic activity by the hop flavonoid xanthohumol:: NF-κB and Akt as targets [J].
Albini, A ;
Dell'Eva, R ;
Vené, R ;
Ferrari, N ;
Buhler, DR ;
Noonan, DM ;
Fassina, G .
FASEB JOURNAL, 2005, 19 (14) :527-+
[2]   High-performance liquid chromatographic determination of xanthohumol in rat plasma, urine, and fecal samples [J].
Avula, B ;
Ganzera, M ;
Warnick, JE ;
Feltenstein, MW ;
Sufka, KJ ;
Khan, IA .
JOURNAL OF CHROMATOGRAPHIC SCIENCE, 2004, 42 (07) :378-382
[3]   Liver fibrosis [J].
Bataller, R ;
Brenner, DA .
JOURNAL OF CLINICAL INVESTIGATION, 2005, 115 (02) :209-218
[4]   Pharmacological IKK2 inhibition blocks liver steatosis and initiation of non-alcoholic steatohepatitis [J].
Beraza, N. ;
Malato, Y. ;
Borght, S. Vander ;
Liedtke, C. ;
Wasmuth, H. E. ;
Dreano, M. ;
de Vos, R. ;
Roskams, T. ;
Trautwein, C. .
GUT, 2008, 57 (05) :655-663
[5]   Cryptogenic cirrhosis: Clinical characterization and risk factors for underlying disease [J].
Caldwell, SH ;
Oelsner, DH ;
Iezzoni, JC ;
Hespenheide, EE ;
Battle, EH ;
Driscoll, CJ .
HEPATOLOGY, 1999, 29 (03) :664-669
[6]   The chalcone xanthohumol inhibits triglyceride and apolipoprotein B secretion in HepG2 cells [J].
Casaschi, A ;
Maiyoh, GK ;
Rubio, BK ;
Li, RW ;
Adeli, K ;
Theriault, AG .
JOURNAL OF NUTRITION, 2004, 134 (06) :1340-1346
[7]   Xanthohumol, a prenylflavonoid derived from hops induces apoptosis and inhibits NF-kappaB activation in prostate epithelial cells [J].
Colgate, Emily C. ;
Miranda, Cristobal L. ;
Stevens, Jan F. ;
Bray, Tammy M. ;
Ho, Emily .
CANCER LETTERS, 2007, 246 (1-2) :201-209
[8]   Free fatty acid-induced inhibition of glucose and insulin-like growth factor I-induced deoxyribonucleic acid synthesis in the pancreatic β-cell line INS-1 [J].
Cousin, SP ;
Hügl, SR ;
Wrede, CE ;
Kajio, H ;
Myers, MG ;
Rhodes, CJ .
ENDOCRINOLOGY, 2001, 142 (01) :229-240
[9]   AKT/NF-κB inhibitor xanthohumol targets cell growth and angiogenesis in hematologic malignancies [J].
Dell'Eva, Raffaella ;
Ambrosini, Claudia ;
Vannini, Nicola ;
Piaggio, Glovanna ;
Albini, Adriana ;
Ferrari, Nicoletta .
CANCER, 2007, 110 (09) :2007-2011
[10]   Anti-proliferative properties of prenylated flavonoids from hops (Humulus lupulus L.) in human prostate cancer cell lines [J].
Delmulle, L. ;
Bellahcene, A. ;
Dhooge, W. ;
Comhaire, F. ;
Roelens, F. ;
Huvaere, K. ;
Heyerick, A. ;
Castronovo, V. ;
De Keukeleire, D. .
PHYTOMEDICINE, 2006, 13 (9-10) :732-734