The use of adipose tissue-conditioned media to demonstrate the differential effects of fat depots on insulin-stimulated glucose uptake in a skeletal muscle cell line

被引:13
作者
Lam, Yan Y. [1 ,2 ]
Janovska, Alena [2 ]
McAinch, Andrew J. [2 ,3 ]
Belobrajdic, Damien P. [4 ]
Hatzinikolas, George [2 ]
Game, Philip [5 ]
Wittert, Gary A. [2 ]
机构
[1] Univ Sydney, Boden Inst Obes Nutr & Exercise, Sydney, NSW 2006, Australia
[2] Univ Adelaide, Discipline Med, Adelaide, SA 5005, Australia
[3] Victoria Univ, Sch Biomed & Hlth Sci, Melbourne, Vic 3000, Australia
[4] CSIRO Food & Nutr Sci, Adelaide, SA 5000, Australia
[5] Univ Adelaide, Discipline Surg, Adelaide, SA 5005, Australia
关键词
Adipokines; Skeletal muscle; Insulin resistance; NECROSIS-FACTOR-ALPHA; FACTOR-KAPPA-B; GLUT4; TRANSLOCATION; DIABETES-MELLITUS; RESISTANCE; OBESITY; METABOLISM; WOMEN; ADIPONECTIN; ADIPOCYTES;
D O I
10.1016/j.orcp.2010.12.002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We aimed to study the depot-specific effect of adipose tissue on insulin sensitivity of skeletal muscle in vitro. Adipose tissue-conditioned medium (CM) was generated from visceral and subcutaneous fat from obese subjects. CM from visceral as compared to subcutaneous fat had higher concentrations of interleukin (IL)-6 (15-fold; P < 0.05) and IL-8 (8-fold; P < 0.05). CM from visceral fat (1: 128 dilution) reduced insulin-stimulated glucose uptake in L6 myotubes by 19% (P < 0.05), an effect mediated by a nuclear factor kappa B (NF kappa B)/mammalian target of rapamycin complex 1 (mTORC1)-dependent pathway and partially reversed by neutralizing IL-6. IL-6 at a concentration comparable to that in CM from visceral fat reduced insulin-stimulated glucose uptake by 53% (P < 0.05), an effect abolished by inhibiting NF kappa B or mTORC1. We demonstrated the utility of the CM-myotube system and identified IL-6 as a major cytokine mediating visceral fat-induced muscle insulin resistance. (C) 2010 Asian Oceanian Association for the Study of Obesity. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:E43 / E54
页数:12
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