Fearnside Jane F, Dumas Marc-Emmanuel, Rothwell Alice R, Wilder Steven P, Cloarec Olivier, Toye Ayo, Blancher Christine, Holmes Elaine, Tatoud Roger, Barton Richard H, Scott James, Nicholson Jeremy K, Gauguier Dominique
The Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.
PLoS One. 2008 Feb 27;3(2):e1668. doi: 10.1371/journal.pone.0001668.
Insulin resistance plays a central role in type 2 diabetes and obesity, which develop as a consequence of genetic and environmental factors. Dietary changes including high fat diet (HFD) feeding promotes insulin resistance in rodent models which present useful systems for studying interactions between genetic background and environmental influences contributing to disease susceptibility and progression. We applied a combination of classical physiological, biochemical and hormonal studies and plasma (1)H NMR spectroscopy-based metabonomics to characterize the phenotypic and metabotypic consequences of HFD (40%) feeding in inbred mouse strains (C57BL/6, 129S6, BALB/c, DBA/2, C3H) frequently used in genetic studies. We showed the wide range of phenotypic and metabonomic adaptations to HFD across the five strains and the increased nutrigenomic predisposition of 129S6 and C57BL/6 to insulin resistance and obesity relative to the other strains. In contrast mice of the BALB/c and DBA/2 strains showed relative resistance to HFD-induced glucose intolerance and obesity. Hierarchical metabonomic clustering derived from (1)H NMR spectral data of the strains provided a phylometabonomic classification of strain-specific metabolic features and differential responses to HFD which closely match SNP-based phylogenetic relationships between strains. Our results support the concept of genomic clustering of functionally related genes and provide important information for defining biological markers predicting spontaneous susceptibility to insulin resistance and pathological adaptations to fat feeding.
胰岛素抵抗在2型糖尿病和肥胖症中起着核心作用,这两种疾病是由遗传和环境因素共同导致的。包括高脂饮食(HFD)喂养在内的饮食变化会促进啮齿动物模型中的胰岛素抵抗,这些模型为研究遗传背景与环境影响之间的相互作用提供了有用的系统,而这种相互作用会影响疾病易感性和进展。我们综合运用经典生理学、生物化学和激素研究以及基于血浆氢核磁共振波谱的代谢组学,来表征在遗传研究中常用的近交小鼠品系(C57BL/6、129S6、BALB/c、DBA/2、C3H)中高脂饮食(40%)喂养后的表型和代谢型后果。我们发现,这五个品系对高脂饮食有广泛的表型和代谢组学适应性,并且相对于其他品系,129S6和C57BL/6对胰岛素抵抗和肥胖症的营养基因组易感性增加。相比之下,BALB/c和DBA/2品系的小鼠对高脂饮食诱导的葡萄糖不耐受和肥胖表现出相对抗性。从这些品系的氢核磁共振波谱数据得出的分层代谢组学聚类,提供了菌株特异性代谢特征的系统发育代谢组学分类以及对高脂饮食的差异反应,这些反应与基于单核苷酸多态性的品系间系统发育关系密切匹配。我们的结果支持功能相关基因的基因组聚类概念,并为定义预测胰岛素抵抗自发易感性和对脂肪喂养的病理适应性的生物标志物提供了重要信息。