Linus Pauling Institute, Oregon State University, Corvallis, OR 97331, USA.
Phytochemistry. 2013 Jul;91:236-41. doi: 10.1016/j.phytochem.2012.04.018. Epub 2012 May 27.
Obesity contributes to increased risk for several chronic diseases including cardiovascular disease and type 2 diabetes. Xanthohumol, a prenylated flavonoid from hops (Humulus lupulus), was tested for efficacy on biomarkers of metabolic syndrome in 4 week old Zucker fa/fa rats, a rodent model of obesity. Rats received daily oral doses of xanthohumol at 0, 1.86, 5.64, and 16.9 mg/kg BW for 6 weeks. All rats were maintained on a high fat (60% kcal) AIN-93G diet for 3 weeks to induce severe obesity followed by a normal AIN-93G (15% kcal fat) diet for the last 3 weeks of the study. Weekly food intake and body weight were recorded. Plasma cholesterol, glucose, insulin, triglyceride, and monocyte chemoattractant protein-1 (MCP-1) levels were assessed using commercial assay kits. Plasma and liver tissue levels of XN and its metabolites were determined by liquid-chromatography tandem mass spectrometry. Plasma and liver tissue levels of xanthohumol were similar between low and medium dose groups and significantly (p<0.05) elevated in the highest dose group. There was a dose-dependent effect on body weight and plasma glucose levels. The highest dose group (n=6) had significantly lower plasma glucose levels compared to the control group (n=6) in male but not female rats. There was also a significant decrease in body weight for male rats in the highest dose group (16.9 mg/kg BW) compared to rats that received no xanthohumol, which was also not seen for female rats. Plasma cholesterol, insulin, triglycerides, and MCP-1 as well as food intake were not affected by treatment. The findings suggest that xanthohumol has beneficial effects on markers of metabolic syndrome.
肥胖会增加患多种慢性疾病的风险,包括心血管疾病和 2 型糖尿病。黄腐酚是一种来自啤酒花(Humulus lupulus)的类黄酮,研究人员对其在 4 周龄 Zucker fa/fa 大鼠(肥胖啮齿动物模型)的代谢综合征生物标志物中的功效进行了测试。大鼠接受了 6 周的每日口服黄腐酚剂量,剂量分别为 0、1.86、5.64 和 16.9mg/kg BW。所有大鼠均在高脂肪(60%卡路里)AIN-93G 饮食中维持 3 周,以诱导严重肥胖,然后在研究的最后 3 周中恢复正常 AIN-93G(15%卡路里脂肪)饮食。每周记录食物摄入量和体重。使用商业检测试剂盒评估血浆胆固醇、葡萄糖、胰岛素、甘油三酯和单核细胞趋化蛋白-1(MCP-1)水平。通过液-质联用色谱法测定血浆和肝组织中 XN 及其代谢物的水平。低剂量和中剂量组的血浆和肝组织中黄腐酚水平相似,高剂量组的水平显著升高(p<0.05)。体重和血浆葡萄糖水平呈剂量依赖性变化。最高剂量组(n=6)雄性大鼠的血浆葡萄糖水平明显低于对照组(n=6),而雌性大鼠则无差异。最高剂量组(16.9mg/kg BW)雄性大鼠的体重也明显下降,而雌性大鼠则无此现象。雄性大鼠的血浆胆固醇、胰岛素、甘油三酯和 MCP-1以及食物摄入量不受治疗影响。研究结果表明,黄腐酚对代谢综合征标志物有有益的影响。