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高能消化效率和脂质代谢改变导致 BFMI 小鼠肥胖。

High energy digestion efficiency and altered lipid metabolism contribute to obesity in BFMI mice.

机构信息

Animal Physiology, Institute of Biology, Philipps-Universität Marburg, Marburg, Germany.

出版信息

Obesity (Silver Spring). 2009 Nov;17(11):1988-93. doi: 10.1038/oby.2009.124. Epub 2009 Apr 23.


DOI:10.1038/oby.2009.124
PMID:19390516
Abstract

To constitute a valuable resource to identify individual genes involved in the development of obesity, a novel mouse model, the Berlin Fat Mouse Inbred line 860 (BFMI860), was established. In order to characterize energy intake and energy expenditure in obese BFMI860 mice, we performed two independent sets of experiments in male BFMI860 and B6 control mice (10 per line). In experiment 1, we analyzed body fat content noninvasively by dual-energy X-ray absorptiometry and measured resting metabolic rate at thermoneutrality (RMRt) and respiratory quotient (RQ) in week 6, 10, and 18. In a second experiment, energy digested (energy intake minus fecal energy loss) was determined by bomb calorimetry from week 6 through week 12. BFMI860 mice were heavier and had higher fat mass (final body fat content was 24.7% compared with 14.6% in B6). They also showed fatty liver syndrome. High body fat accumulation in BFMI860 mice was restricted to weeks 6-10 and was accompanied by hyperphagia, higher energy digestion, higher RQs, and abnormally high blood triglyceride levels. Lean mass-adjusted RMRt was not altered between lines. These results indicate that in BFMI860 mice, the excessive accumulation of body fat is associated with altered lipid metabolism, high energy intake, and energy digestion. Assuming that BFMI860 mice and their obese phenotypes are of polygenic nature, this line is an excellent model for the study of obesity in humans, especially for juvenile obesity and hyperlipidemia.

摘要

为了确定与肥胖症发生有关的个体基因,我们建立了一种新的小鼠模型,即柏林肥胖易感近交系 860 号(BFMI860)。为了研究肥胖 BFMI860 小鼠的能量摄入和能量消耗,我们在雄性 BFMI860 和 B6 对照小鼠(每条线 10 只)中进行了两组独立的实验。在实验 1 中,我们通过双能 X 射线吸收仪非侵入性地分析体脂含量,并在第 6、10 和 18 周测量常温下的基础代谢率(RMRt)和呼吸商(RQ)。在第二项实验中,通过弹式热量计从第 6 周到第 12 周测定消化的能量(能量摄入减去粪便能量损失)。BFMI860 小鼠体重更重,体脂含量更高(最终体脂肪含量为 24.7%,而 B6 为 14.6%)。它们还表现出脂肪肝综合征。BFMI860 小鼠的体脂过度积累仅限于第 6-10 周,同时伴有食欲亢进、更高的能量消化、更高的 RQ 和异常高的血甘油三酯水平。两条线之间的去脂体重校正后的 RMRt 没有改变。这些结果表明,在 BFMI860 小鼠中,体脂肪的过度积累与脂质代谢改变、能量摄入增加和能量消化有关。假设 BFMI860 小鼠及其肥胖表型具有多基因性质,那么该系是研究人类肥胖症的理想模型,尤其是青少年肥胖症和高血脂症。

相似文献

[1]
High energy digestion efficiency and altered lipid metabolism contribute to obesity in BFMI mice.

Obesity (Silver Spring). 2009-4-23

[2]
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引用本文的文献

[1]
Strain and Depot-specific Differences in Adipose Tissues of Obese BFMI Mice.

In Vivo. 2023

[2]
Circadian PER1 controls daily fat absorption with the regulation of PER1-PKA on phosphorylation of bile acid synthetase.

J Lipid Res. 2023-6

[3]
A deletion containing a CTCF-element in intron 8 of the Bbs7 gene is partially responsible for juvenile obesity in the Berlin Fat Mouse.

Mamm Genome. 2022-9

[4]
Fine mapping a major obesity locus (jObes1) using a Berlin Fat Mouse × B6N advanced intercross population.

Int J Obes (Lond). 2016-11

[5]
The direction of cross affects [corrected] obesity after puberty in male but not female offspring.

BMC Genomics. 2015-11-6

[6]
Changes in metabolite profiles caused by genetically determined obesity in mice.

Metabolomics. 2014

[7]
The age of attaining highest body weight correlates with lifespan in a genetically obese mouse model.

Nutr Diabetes. 2013-3-18

[8]
Features of the metabolic syndrome in the Berlin Fat Mouse as a model for human obesity.

Obes Facts. 2011-7-26

[9]
Genetic and diet effects on Ppar-α and Ppar-γ signaling pathways in the Berlin Fat Mouse Inbred line with genetic predisposition for obesity.

Lipids Health Dis. 2010-9-10

[10]
High-fat diet leads to a decreased methylation of the Mc4r gene in the obese BFMI and the lean B6 mouse lines.

J Appl Genet. 2010

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