Xanthohumol, a hop-derived prenylated flavonoid, promotes macrophage reverse cholesterol transport

被引:27
作者
Hirata, Hiroshi [1 ]
Uto-Kondo, Harumi [2 ,4 ]
Ogura, Masatsune [2 ,5 ]
Ayaori, Makoto [3 ]
Shiotani, Kazusa [2 ]
Ota, Ami [1 ]
Tsuchiya, Youichi [1 ]
Ikewaki, Katsunori [2 ]
机构
[1] SAPPORO HOLDINGS LTD, Frontier Labs Value Creat, 10 Okatome, Yaizu, Shizuoka 4250013, Japan
[2] Natl Def Med Coll, Dept Internal Med, Div Neurol Antiaging & Vasc Med, 3-2 Namiki, Tokorozawa, Saitama 3598513, Japan
[3] Tokorozawa Heart Ctr, 1-4-1-101 Midoricho, Tokorozawa, Saitama 3591111, Japan
[4] Nihon Univ, Dept Biosci Daily Life, Coll Bioresource Sci, 1866 Kameino, Fujisawa, Kanagawa 2520880, Japan
[5] Natl Cerebral & Cardiovasc Ctr, Res Inst, Dept Mol Innovat Lipidol, 5-7-1 Fujishirodai, Suita, Osaka 5658565, Japan
关键词
Xanthohumol; Reverse cholesterol transport; Cholesterol efflux; HDL cholesterol; Hop; HIGH-DENSITY-LIPOPROTEIN; ESTER TRANSFER PROTEIN; LIVER-X-RECEPTOR; BILE-SALT TRANSPORTERS; HUMULUS-LUPULUS L; HDL-CHOLESTEROL; GLUCOSE-METABOLISM; HEPATIC STEATOSIS; LDL CHOLESTEROL; IN-VITRO;
D O I
10.1016/j.jnutbio.2017.04.011
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
Xanthohumol, a prominent prenyl flavonoid from the hop plant (Humulus lupulus L.), is suggested to be antiatherogenic since it reportedly increases high-density lipoprotein (HDL) cholesterol levels. It is not clear whether xanthohumol promotes reverse cholesterol transport (RCT), the most important antiatherogenic property of HDL; therefore, we investigated the effects of xanthohumol on macrophage-to-feces RCT using a hamster model as a CETP-expressing species. In vivo RCT experiments showed that xanthohumol significantly increased fecal appearance of the tracer derived from intraperitoneally injected [H-3]-cholesterol-labeled macrophages. Ex vivo experiments were then employed to investigate the detailed mechanism by which xanthohumol enhanced RCT. Cholesterol efflux capacity from macrophages was 1.5-fold higher in xanthohumol-fed hamsters compared with the control group. In addition, protein expression and lecithin-cholesterol acyltransferase activity in the HDL fraction were significantly higher in xanthohumol-fed hamsters compared with the control, suggesting that xanthohumol promoted HDL maturation. Hepatic transcript analysis revealed that xanthohumol increased mRNA expression of abcg8 and cyp7a1. In addition, protein expressions of liver X receptor alpha and bile pump export protein were increased in the liver by xanthohumol administration when compared with the control, implying that it stimulated bile acid synthesis and cholesterol excretion to feces. In conclusion, our data demonstrate that xanthohumol improves RCT in vivo through cholesterol efflux from macrophages and excretion to feces, leading to antiatheroscierosis effects. It remains to be elucidated whether enhancement of RCT by xanthohumol could prove valuable in humans. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:29 / 34
页数:6
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