在喂食西方饮食的小鼠中,液态果糖会损害肝脏胰岛素信号传导,并导致胆固醇和甘油三酯堆积,而不会改变热量摄入和体重。
Liquid fructose in Western-diet-fed mice impairs liver insulin signaling and causes cholesterol and triglyceride loading without changing calorie intake and body weight.
作者信息
Baena Miguel, Sangüesa Gemma, Hutter Natalia, Beltrán José María, Sánchez Rosa María, Roglans Núria, Alegret Marta, Laguna Juan Carlos
机构信息
Department of Pharmacology, Toxicology and Therapeutic Chemistry, School of Pharmacy and Food Science, University of Barcelona, Spain; Institute of Biomedicine University of Barcelona, Spain.
Department of Pharmacology, Toxicology and Therapeutic Chemistry, School of Pharmacy and Food Science, University of Barcelona, Spain.
出版信息
J Nutr Biochem. 2017 Feb;40:105-115. doi: 10.1016/j.jnutbio.2016.10.015. Epub 2016 Nov 2.
BACKGROUND/OBJECTIVES: Liquid fructose associates with prevalence of type 2 diabetes mellitus and obesity. Intervention studies suggest that metabolically unfit individuals are more responsive than healthy individuals to liquid fructose. We determined whether mice consuming an obesogenic Western diet were more responsive than chow-fed mice to the alterations induced by liquid fructose supplementation (LFS).
METHODS
C57BL/6N mice were fed chow or Western diet±ad libitum 15% fructose solution for 12 weeks. Food and liquid intake and body weight were monitored. Plasma analytes and liver lipids, histology and the expression of genes related to lipid handling, endoplasmic reticulum stress, inflammation and insulin signaling were analyzed.
RESULTS
Western diet increased energy intake, visceral adipose tissue (vWAT), body weight, plasma and liver triglycerides and cholesterol, and inflammatory markers in vWAT vs. chow-fed mice. LFS did not change energy intake, vWAT or body weight. LFS significantly increased plasma and liver triglycerides and cholesterol levels only in Western-diet-fed mice. These changes associated with a potentiation of the increased liver expression of PPARγ and CD36 that was observed in Western-fed mice and related to the increased liver mTOR phosphorylation induced by LFS. Furthermore, LFS in Western-diet-fed mice induced the largest reduction in liver IRS2 protein and a significant decrease in whole-body insulin sensitivity.
CONCLUSIONS
LFS in mice, in a background of an unhealthy diet that already induces fatty liver visceral fat accretion and obesity, increases liver lipid burden, hinders hepatic insulin signaling and diminishes whole-body insulin sensitivity without changing energy intake.
背景/目的:液态果糖与2型糖尿病和肥胖症的患病率相关。干预研究表明,代谢不健康的个体比健康个体对液态果糖的反应更强烈。我们确定了食用致肥胖西方饮食的小鼠是否比食用普通饲料的小鼠对补充液态果糖(LFS)引起的变化更敏感。
方法
将C57BL/6N小鼠分为两组,分别喂食普通饲料或西方饮食,并随意给予15%果糖溶液,持续12周。监测食物和液体摄入量以及体重。分析血浆分析物、肝脏脂质、组织学以及与脂质处理、内质网应激、炎症和胰岛素信号相关的基因表达。
结果
与喂食普通饲料的小鼠相比,西方饮食增加了能量摄入、内脏脂肪组织(vWAT)、体重、血浆和肝脏甘油三酯及胆固醇,以及vWAT中的炎症标志物。LFS并未改变能量摄入、vWAT或体重。LFS仅在喂食西方饮食的小鼠中显著增加了血浆和肝脏甘油三酯及胆固醇水平。这些变化与西方饮食喂养小鼠中观察到的肝脏PPARγ和CD36表达增加的增强有关,并且与LFS诱导的肝脏mTOR磷酸化增加有关。此外,西方饮食喂养小鼠中的LFS导致肝脏IRS2蛋白的最大减少以及全身胰岛素敏感性的显著降低。
结论
在已经导致脂肪肝、内脏脂肪堆积和肥胖的不健康饮食背景下,小鼠中的LFS增加了肝脏脂质负担,阻碍了肝脏胰岛素信号传导,并降低了全身胰岛素敏感性,而没有改变能量摄入。