Liquid fructose in Western-diet-fed mice impairs liver insulin signaling and causes cholesterol and triglyceride loading without changing calorie intake and body weight

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• 作者：Miguel Baena^a ; ^b ; ¹ ; Gemma Sangü ; esa^a ; ^b ; ¹ ; Natalia Hutter^a ; José ; Marí ; a Beltrá ; n^a ; Rosa Marí ; a Sá ; nchez^a ; ^b ; ^c ; Nú ; ria Roglans^a ; ^b ; ^c ; Marta Alegret^a ; ^b ; ^c ; ¹ ; ^{alegret@ub.edu} ; Juan Carlos Laguna^a ; ^b ; ^c ; ¹ ; ^{jclagunae@ub.edu}
• 关键词：ChREBP ; IRS2 ; PPARγ ; CD36 ; mTOR ; Visceral adipose tissue ; Leptin
• 刊名：The Journal of Nutritional Biochemistry
• 出版年：2017
• 出版时间：February 2017
• 年：2017
• 卷：40
• 期：Complete
• 页码：105-115
• 全文大小：1433 K
• 卷排序：40

文摘

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).MethodsC57BL/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.ResultsWestern 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.ConclusionsLFS 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.