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黄腐酚可改善饮食诱导的肥胖C57BL/6J小鼠的葡萄糖和脂质代谢功能障碍。

Xanthohumol improves dysfunctional glucose and lipid metabolism in diet-induced obese C57BL/6J mice.

作者信息

Miranda Cristobal L, Elias Valerie D, Hay Joshua J, Choi Jaewoo, Reed Ralph L, Stevens Jan F

机构信息

Linus Pauling Institute and Department of Pharmaceutical Sciences, College of Pharmacy, Oregon State University, Corvallis, OR, USA.

Linus Pauling Institute and Department of Pharmaceutical Sciences, College of Pharmacy, Oregon State University, Corvallis, OR, USA.

出版信息

Arch Biochem Biophys. 2016 Jun 1;599:22-30. doi: 10.1016/j.abb.2016.03.008. Epub 2016 Mar 11.

Abstract

Xanthohumol (XN) is a prenylated flavonoid found in hops (Humulus lupulus) and beer. The dose-dependent effects of XN on glucose and lipid metabolism in a preclinical model of metabolic syndrome were the focus of our study. Forty-eight male C57BL/6J mice, 9 weeks of age, were randomly divided into three XN dose groups of 16 animals. The mice were fed a high-fat diet (60% kcal as fat) supplemented with XN at dose levels of 0, 30, or 60 mg/kg body weight/day, for 12 weeks. Dietary XN caused a dose-dependent decrease in body weight gain. Plasma levels of glucose, total triglycerides, total cholesterol, and MCP-1 were significantly decreased in mice on the 60 mg/kg/day treatment regimen. Treatment with XN at 60 mg/kg/day resulted in reduced plasma LDL-cholesterol (LDL-C), IL-6, insulin and leptin levels by 80%, 78%, 42%, and 41%, respectively, compared to the vehicle control group. Proprotein Convertase Subtilisin Kexin 9 (PCSK-9) levels were 44% lower in the 60 mg/kg dose group compared to the vehicle control group (p ≤ 0.05) which may account for the LDL-C lowering activity of XN. Our results show that oral administration of XN improves markers of systemic inflammation and metabolic syndrome in diet-induced obese C57BL/6J mice.

摘要

黄腐酚(XN)是一种异戊烯基黄酮,存在于啤酒花(Humulus lupulus)和啤酒中。本研究聚焦于XN在代谢综合征临床前模型中对葡萄糖和脂质代谢的剂量依赖性影响。将48只9周龄的雄性C57BL/6J小鼠随机分为三个XN剂量组,每组16只动物。给小鼠喂食高脂肪饮食(脂肪提供60%的千卡热量),并分别补充剂量为0、30或60毫克/千克体重/天的XN,持续12周。饮食中的XN导致体重增加呈剂量依赖性下降。在60毫克/千克/天的治疗方案下,小鼠血浆中的葡萄糖、总甘油三酯、总胆固醇和MCP-1水平显著降低。与溶剂对照组相比,60毫克/千克/天的XN治疗使血浆低密度脂蛋白胆固醇(LDL-C)、白细胞介素-6、胰岛素和瘦素水平分别降低了80%、78%、42%和41%。与溶剂对照组相比,60毫克/千克剂量组的前蛋白转化酶枯草杆菌蛋白酶9(PCSK-9)水平降低了44%(p≤0.05),这可能是XN降低LDL-C活性的原因。我们的结果表明,口服XN可改善饮食诱导肥胖的C57BL/6J小鼠的全身炎症和代谢综合征指标。

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