Suppr超能文献

在曾经肥胖的小鼠中,脂肪细胞基因表达会发生改变,并且这种改变是饮食组成的函数。

Adipocyte gene expression is altered in formerly obese mice and as a function of diet composition.

作者信息

Miller Ryan S, Becker Kevin G, Prabhu Vinayakumar, Cooke David W

机构信息

Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.

出版信息

J Nutr. 2008 Jun;138(6):1033-8. doi: 10.1093/jn/138.6.1033.

Abstract

In the development of obesity, the source of excess energy may influence appetite and metabolism. To determine the effects of differences in diet composition in obesity, mice were fed either a high-carbohydrate diet (HC; 10% fat energy) or a high-fat energy-restricted diet (HFR; 60% fat energy) over 18 wk in weight-matched groups of mice. To identify obesity-associated genes with persistently altered expression following weight reduction, mice were fed either a standard low-fat diet (LF; 10% fat energy), an unrestricted high-fat diet (HF; 60% fat energy), or a HF diet followed by weight reduction (WR). Mice fed a HF diet had significantly greater gonadal fat mass and higher whole blood glucose concentrations than mice fed an HC diet. Of the mice fed a high-fat diet, total body weight and serum insulin concentrations were greater in HF than in HFR. Microarray analysis revealed that HF vs. HC feeding resulted in global differences in adipocyte gene expression patterns. Although we identified genes whose expression was altered in both moderately and severely obese mice, there were also a large number of genes with altered expression only in severe obesity. Formerly obese, WR mice did not differ significantly from lean controls in total body weight or physiological measures. However, microarray analysis revealed distinctly different patterns of adipocyte gene expression. Furthermore, there were 398 genes with altered expression in HF mice that persisted in WR mice. Genes with persistently altered expression following obesity may play a role in rebound weight gain following weight reduction.

摘要

在肥胖症的发展过程中,多余能量的来源可能会影响食欲和新陈代谢。为了确定肥胖症中饮食成分差异的影响,在体重匹配的小鼠组中,让小鼠在18周内分别食用高碳水化合物饮食(HC;10%脂肪能量)或高脂肪能量限制饮食(HFR;60%脂肪能量)。为了识别体重减轻后表达持续改变的肥胖相关基因,让小鼠分别食用标准低脂饮食(LF;10%脂肪能量)、无限制高脂肪饮食(HF;60%脂肪能量)或先食用高脂肪饮食然后减重(WR)。与食用HC饮食的小鼠相比,食用HF饮食的小鼠性腺脂肪量显著更高,全血葡萄糖浓度也更高。在食用高脂肪饮食的小鼠中,HF组的总体重和血清胰岛素浓度高于HFR组。微阵列分析显示,HF喂养与HC喂养导致脂肪细胞基因表达模式存在整体差异。虽然我们鉴定出了在中度和重度肥胖小鼠中表达均发生改变的基因,但也有大量基因仅在重度肥胖时表达发生改变。曾经肥胖的WR小鼠在总体重或生理指标上与瘦对照组没有显著差异。然而,微阵列分析显示脂肪细胞基因表达模式明显不同。此外,在HF小鼠中表达改变的398个基因在WR小鼠中持续存在。肥胖后表达持续改变的基因可能在体重减轻后的体重反弹中起作用。

相似文献

3
At similar weight loss, dietary composition determines the degree of glycemic improvement in diet-induced obese C57BL/6 mice.
PLoS One. 2018 Jul 23;13(7):e0200779. doi: 10.1371/journal.pone.0200779. eCollection 2018.
9
Fat, carbohydrate, and calories in the development of diabetes and obesity in the C57BL/6J mouse.
Metabolism. 2004 Apr;53(4):454-7. doi: 10.1016/j.metabol.2003.11.018.
10
High-fat hypocaloric diet modifies carbohydrate utilization of obese rats during weight loss.
Am J Physiol Endocrinol Metab. 2001 May;280(5):E797-803. doi: 10.1152/ajpendo.2001.280.5.E797.

引用本文的文献

1
Ceramide-induced FGF13 impairs systemic metabolic health.
Cell Metab. 2025 May 6;37(5):1206-1222.e8. doi: 10.1016/j.cmet.2025.03.002. Epub 2025 Mar 31.
3
4
5
Weight Regain in Formerly Obese Mice Hastens Development of Hepatic Steatosis Due to Impaired Adipose Tissue Function.
Obesity (Silver Spring). 2020 Jun;28(6):1086-1097. doi: 10.1002/oby.22788. Epub 2020 Apr 13.
8
Macrophage Proliferation Sustains Adipose Tissue Inflammation in Formerly Obese Mice.
Diabetes. 2017 Feb;66(2):392-406. doi: 10.2337/db16-0500. Epub 2016 Nov 8.

本文引用的文献

1
Brain adipocytokine action and metabolic regulation.
Diabetes. 2006 Dec;55 Suppl 2:S145-54. doi: 10.2337/db06-s018.
2
A rapid method for microarray cross platform comparisons using gene expression signatures.
Mol Cell Probes. 2007 Feb;21(1):35-46. doi: 10.1016/j.mcp.2006.07.004. Epub 2006 Aug 10.
4
Prevalence of overweight and obesity in the United States, 1999-2004.
JAMA. 2006 Apr 5;295(13):1549-55. doi: 10.1001/jama.295.13.1549.
5
A network-based analysis of systemic inflammation in humans.
Nature. 2005 Oct 13;437(7061):1032-7. doi: 10.1038/nature03985. Epub 2005 Aug 31.
6
Different forms of obesity as a function of diet composition.
Int J Obes (Lond). 2005 Nov;29(11):1368-78. doi: 10.1038/sj.ijo.0803017.
7
Endocrine and signalling role of adipose tissue: new perspectives on fat.
Acta Physiol Scand. 2005 Aug;184(4):285-93. doi: 10.1111/j.1365-201X.2005.01468.x.
9
Obesity-related differential gene expression in the visceral adipose tissue.
Obes Surg. 2005 Jun-Jul;15(6):758-65. doi: 10.1381/0960892054222876.
10
Weight loss regulates inflammation-related genes in white adipose tissue of obese subjects.
FASEB J. 2004 Nov;18(14):1657-69. doi: 10.1096/fj.04-2204com.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验