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健康人短期过量进食后骨骼肌细胞外基质重塑

Skeletal muscle extracellular matrix remodeling after short-term overfeeding in healthy humans.

作者信息

Tam Charmaine S, Chaudhuri Rima, Hutchison Amy T, Samocha-Bonet Dorit, Heilbronn Leonie K

机构信息

Charles Perkins Centre and School of Life and Environmental Sciences, University of Sydney, New South Wales, Australia.

Charles Perkins Centre, School of Molecular Bioscience, School of Medicine, University of Sydney, Sydney, New South Wales, Australia.

出版信息

Metabolism. 2017 Feb;67:26-30. doi: 10.1016/j.metabol.2016.10.009. Epub 2016 Oct 28.

Abstract

BACKGROUND

Skeletal muscle extracellular matrix (ECM) remodeling has been proposed as a feature of the pathogenic milieu associated with obesity and metabolic dysfunction. The aim of the current study was to examine the timeline of this response and determine whether 3 and 28days of overfeeding alters markers of ECM turnover.

METHODS

Forty healthy individuals were overfed by 1250kcal/day for 28days. Hyperinsulinemic-euglycemic clamps and abdominal fat distribution were performed at baseline and day 28 of overfeeding and skeletal muscle biopsies taken at baseline, day 3 and day 28. mRNA expression (COL1a1, COL3a1, MMP2, MMP9, TIMP1, CD68, Integrin) was performed in 19 subjects that consented to having all biopsies performed and microarray analysis was performed in 8 participants at baseline and day 28.

RESULTS

In the whole cohort, body weight increased by 0.6±0.1 and 2.7±0.3kg at days 3 and 28 (both P<0.001), respectively. Glucose infusion rate during the hyperinsulinemic-euglycemic clamp decreased from 54.8±2.8 at baseline to 50.3±2.5μmol/min/kg FFM at day 28 of overfeeding (P=0.03). Muscle COL1 and COL3 and MMP2 mRNA levels were significantly higher 28days after overfeeding (all P<0.05), with no significant changes in MMP9, TIMP1, CD68 and integrin expression. Microarray based gene set tests revealed that pathways related to ECM receptor interaction, focal adhesion and adherens junction were differentially altered.

CONCLUSIONS

Skeletal muscle ECM remodeling occurs early in response to over-nutrition with as little as 3% body weight gain. Our findings contribute to the growing evidence linking muscle ECM remodeling and accumulation as another sequela of obesity-related insulin resistance.

摘要

背景

骨骼肌细胞外基质(ECM)重塑被认为是与肥胖和代谢功能障碍相关的致病环境的一个特征。本研究的目的是研究这种反应的时间进程,并确定3天和28天的过度喂养是否会改变ECM周转的标志物。

方法

40名健康个体每天额外摄入1250千卡热量,持续28天。在基线和过度喂养的第28天进行高胰岛素-正常血糖钳夹试验和腹部脂肪分布测量,并在基线、第3天和第28天采集骨骼肌活检样本。对19名同意进行所有活检的受试者进行mRNA表达(COL1a1、COL3a1、MMP2、MMP9、TIMP1、CD68、整合素)检测,并对8名参与者在基线和第28天进行微阵列分析。

结果

在整个队列中,第3天和第28天体重分别增加了0.6±0.1千克和2.7±0.3千克(均P<0.001)。高胰岛素-正常血糖钳夹试验期间的葡萄糖输注率从基线时的54.8±2.8降至过度喂养第28天的50.3±2.5微摩尔/分钟/千克去脂体重(P=0.03)。过度喂养28天后,肌肉COL1、COL3和MMP2的mRNA水平显著升高(均P<0.05),而MMP9、TIMP1、CD68和整合素的表达无显著变化。基于微阵列的基因集测试显示,与ECM受体相互作用、粘着斑和紧密连接相关的通路有差异改变。

结论

骨骼肌ECM重塑在对营养过剩的早期反应中就会发生,体重增加仅3%。我们的研究结果为将肌肉ECM重塑和积累与肥胖相关胰岛素抵抗的另一个后遗症联系起来的越来越多的证据做出了贡献。

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