Netherlands Nutrigenomics Centre, Top Institute Food and Nutrition, Wageningen, The Netherlands.
PLoS One. 2011 Apr 25;6(4):e19145. doi: 10.1371/journal.pone.0019145.
Excessive intake of dietary fat is known to be a contributing factor in the development of obesity. In this study, we determined the dose-dependent effects of dietary fat on the development of this metabolic condition with a focus on changes in gene expression in the small intestine. C57BL/6J mice were fed diets with either 10, 20, 30 or 45 energy% (E%) derived from fat for four weeks (n = 10 mice/diet). We found a significant higher weight gain in mice fed the 30E% and 45E% fat diet compared to mice on the control diet. These data indicate that the main shift towards an obese phenotype lies between a 20E% and 30E% dietary fat intake. Analysis of differential gene expression in the small intestine showed a fat-dose dependent gradient in differentially expressed genes, with the highest numbers in mice fed the 45E% fat diet. The main shift in fat-induced differential gene expression was found between the 30E% and 45E% fat diet. Furthermore, approximately 70% of the differentially expressed genes were changed in a fat-dose dependent manner. Many of these genes were involved in lipid metabolism-related processes and were already differentially expressed on a 30E% fat diet. Taken together, we conclude that up to 20E% of dietary fat, the small intestine has an effective 'buffer capacity' for fat handling. From 30E% of dietary fat, a switch towards an obese phenotype is triggered. We further speculate that especially fat-dose dependently changed lipid metabolism-related genes are involved in development of obesity.
已知膳食脂肪摄入过多是导致肥胖的一个因素。在这项研究中,我们通过关注小肠基因表达的变化,确定了膳食脂肪对这种代谢状况发展的剂量依赖性影响。C57BL/6J 小鼠喂食含 10%、20%、30%或 45%能量(E%)来源于脂肪的饮食 4 周(n=10 只/饮食)。我们发现,喂食 30E%和 45E%脂肪饮食的小鼠体重增加明显高于喂食对照饮食的小鼠。这些数据表明,向肥胖表型的主要转变发生在 20E%和 30E%的膳食脂肪摄入量之间。小肠差异基因表达分析显示,差异基因表达呈脂肪剂量依赖性梯度,喂食 45E%脂肪饮食的小鼠差异基因数量最多。脂肪诱导的差异基因表达的主要转变发生在 30E%和 45E%脂肪饮食之间。此外,大约 70%的差异表达基因呈脂肪剂量依赖性变化。这些基因中的许多与脂质代谢相关过程有关,在 30E%脂肪饮食时就已经有差异表达。综上所述,我们得出结论,小肠对脂肪处理有有效的“缓冲能力”,在摄入 20%的膳食脂肪以内。从 30%的膳食脂肪开始,会引发肥胖表型的转变。我们进一步推测,特别是脂肪剂量依赖性变化的与脂质代谢相关的基因可能参与了肥胖的发展。