首页> 外文期刊>Phytochemistry >Xanthohumol lowers body weight and fasting plasma glucose in obese male Zucker fa/fa rats.
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Xanthohumol lowers body weight and fasting plasma glucose in obese male Zucker fa/fa rats.

机译:Xanthohumol可以降低肥胖的雄性Zucker fa / fa大鼠的体重和空腹血糖。

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摘要

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
机译:肥胖会增加几种慢性疾病的风险,包括心血管疾病和2型糖尿病。 Xanthohumol是一种来自蛇麻草的异黄酮类黄酮,已在4周大的Zucker fa / fa大鼠(一种肥胖的啮齿动物模型)中对代谢综合征的生物标志物进行了测试。大鼠在0、1.86、5.64和16.9 mg / kg BW的剂量下每天口服黄嘌呤酚,持续6周。在研究的最后三周,将所有大鼠维持在高脂肪(60%kcal)AIN-93G饮食中诱导严重肥胖,然后再进行正常AIN-93G(15%kcal脂肪)饮食。记录每周食物摄入量和体重。使用商业化验试剂盒评估血浆胆固醇,葡萄糖,胰岛素,甘油三酸酯和单核细胞趋化蛋白-1(MCP-1)的水平。 XN及其代谢产物的血浆和肝组织水平通过液相色谱串联质谱法测定。在低剂量和中等剂量组之间,黄腐酚的血浆和肝组织水平相似,在最高剂量组中显着(p <0.05)升高。对体重和血浆葡萄糖水平有剂量依赖性的影响。在雄性大鼠而非雌性大鼠中,最高剂量组(n = 6)的血浆葡萄糖水平明显低于对照组(n = 6)。与未接受黄腐酚的大鼠相比,最高剂量组(16.9 mg / kg体重)的雄性大鼠体重也显着降低,雌性大鼠也未见到。血浆胆固醇,胰岛素,甘油三酸酯和MCP-1以及食物摄入量均不受治疗的影响。这些发现表明黄腐酚对代谢综合征的标志物具有有益作用

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