Committee on Molecular Metabolism and Nutrition, University of Chicago, Chicago, Illinois.
Section of Endocrinology, Diabetes and Metabolism, Department of Medicine, University of Chicago, Chicago, Illinois.
Am J Physiol Regul Integr Comp Physiol. 2022 Aug 1;323(2):R255-R266. doi: 10.1152/ajpregu.00174.2021. Epub 2022 May 17.
Increased human consumption of high-fructose corn syrup has been linked to the marked increase in obesity and metabolic syndrome. Previous studies on the rapid effects of a high-fructose diet in mice have largely been confined to the C57BL/6 strains. In the current study, the FVB/N strain of mice that are resistant to diet-induced weight gain were used and fed a control or high-fructose diet for 48 h or for 12 wk. Many of the previously reported changes that occurred upon high-fructose feeding for 48 h in C57BL/6 mice were recapitulated in the FVB/N mice. However, the acute increases in fructolytic and lipogenic gene expression were completely lost during the 12-wk dietary intervention protocol. Furthermore, there was no significant weight gain in FVB/N mice fed a high-fructose diet for 12 wk, despite an overall increase in caloric consumption and an increase in average epididymal adipocyte cell size. These findings may be in part explained by a commensurate increase in energy expenditure and in carbohydrate utilization in high-fructose-fed animals. Overall, these findings demonstrate that FVB/N mice are a suitable model for the study of the effects of dietary intervention on metabolic and molecular parameters. Furthermore, the rapid changes in hepatic gene expression that have been widely reported were not sustained over a longer time course. Compensatory changes in energy expenditure and utilization may be in part responsible for the differences obtained between acute and chronic high-fructose feeding protocols.
人类对高果糖玉米糖浆的消费增加与肥胖和代谢综合征的显著增加有关。先前关于高果糖饮食对小鼠的快速影响的研究主要局限于 C57BL/6 品系。在目前的研究中,使用了对饮食诱导的体重增加具有抗性的 FVB/N 品系小鼠,并在 48 小时或 12 周内用对照或高果糖饮食喂养。在 C57BL/6 小鼠中,在高果糖喂养 48 小时后发生的许多先前报道的变化在 FVB/N 小鼠中得到了重现。然而,在 12 周的饮食干预方案中,急性增加的果糖分解和脂肪生成基因表达完全丧失。此外,尽管 FVB/N 小鼠的总热量消耗增加且附睾脂肪细胞平均大小增加,但在 12 周的高果糖饮食喂养中,它们的体重没有明显增加。这些发现部分可以通过高果糖喂养动物的能量消耗和碳水化合物利用率的相应增加来解释。总的来说,这些发现表明 FVB/N 小鼠是研究饮食干预对代谢和分子参数影响的合适模型。此外,广泛报道的肝脏基因表达的快速变化在较长的时间过程中并没有持续。能量消耗和利用的代偿性变化可能部分解释了急性和慢性高果糖喂养方案之间获得的差异。