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鉴定热量摄入调节的脂肪细胞基因。

Identification of adipocyte genes regulated by caloric intake.

机构信息

Department of Medical and Health Sciences, Linköping University, 581 85 Linköping, Sweden.

出版信息

J Clin Endocrinol Metab. 2011 Feb;96(2):E413-8. doi: 10.1210/jc.2009-2534. Epub 2010 Nov 3.

Abstract

CONTEXT

Changes in energy intake have marked and rapid effects on metabolic functions, and some of these effects may be due to changes in adipocyte gene expression that precede alterations in body weight.

OBJECTIVE

The aim of the study was to identify adipocyte genes regulated by changes in caloric intake independent of alterations in body weight.

RESEARCH DESIGN AND METHODS

Obese subjects given a very low-caloric diet followed by gradual reintroduction of ordinary food and healthy subjects subjected to overfeeding were investigated. Adipose tissue biopsies were taken at multiple time-points, and gene expression was measured by DNA microarray. Genes regulated in the obese subjects undergoing caloric restriction followed by refeeding were identified using two-way ANOVA corrected with Bonferroni. From these, genes regulated by caloric restriction and oppositely during the weight-stable refeeding phase were identified in the obese subjects. The genes that were also regulated, in the same direction as the refeeding phase, in the healthy subjects after overfeeding were defined as being regulated by caloric intake. Results were confirmed using real-time PCR or immunoassay.

RESULTS

Using a significance level of P < 0.05 for all comparisons, 52 genes were down-regulated, and 50 were up-regulated by caloric restriction and regulated in the opposite direction by refeeding and overfeeding. Among these were genes involved in lipogenesis (ACLY, ACACA, FASN, SCD), control of protein synthesis (4EBP1, 4EBP2), β-oxidation (CPT1B), and insulin resistance (PEDF, SPARC).

CONCLUSIONS

Metabolic genes involved in lipogenesis, protein synthesis, and insulin resistance are central in the transcriptional response of adipocytes to changes in caloric intake.

摘要

背景

能量摄入的变化对代谢功能有显著而迅速的影响,其中一些影响可能是由于体重变化之前脂肪细胞基因表达的改变。

目的

本研究旨在鉴定与体重变化无关的热量摄入变化调节的脂肪细胞基因。

研究设计和方法

研究了接受极低热量饮食然后逐渐重新引入普通食物的肥胖患者和接受过饱饮食的健康受试者。在多个时间点采集脂肪组织活检,并通过 DNA 微阵列测量基因表达。使用双向方差分析(ANOVA)对肥胖患者进行校正,Bonferroni 校正后确定热量限制后再喂养时调节的基因。从这些肥胖患者中,确定了在体重稳定再喂养阶段热量限制和相反调节的基因。在过饱饮食后,健康受试者中与再喂养阶段方向相同调节的基因被定义为受热量摄入调节。使用实时 PCR 或免疫测定法确认结果。

结果

使用所有比较的 P < 0.05 显著性水平,52 个基因下调,50 个基因上调,热量限制和再喂养及过饱饮食调节的方向相反。其中包括参与脂肪生成(ACLY、ACACA、FASN、SCD)、蛋白质合成控制(4EBP1、4EBP2)、β-氧化(CPT1B)和胰岛素抵抗(PEDF、SPARC)的基因。

结论

参与脂肪生成、蛋白质合成和胰岛素抵抗的代谢基因是脂肪细胞对热量摄入变化的转录反应的核心。

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