Fatty acid-induced NF-κB activation and insulin resistance in skeletal muscle are chain length dependent

被引:71
|
作者
Hommelberg, Pascal P. H. [1 ,3 ]
Plat, Jogchum [1 ]
Langen, Ramon C. J. [2 ]
Schols, Annemie M. W. J. [2 ]
Mensink, Ronald P. [1 ,3 ]
机构
[1] Maastricht Univ, Dept Human Biol, NL-6200 MD Maastricht, Netherlands
[2] Maastricht Univ, Dept Resp Med, NL-6200 MD Maastricht, Netherlands
[3] Top Inst Food & Nutr, Wageningen, Netherlands
来源
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM | 2009年 / 296卷 / 01期
关键词
glucose transporter 4 translocation; nuclear factor-kappa B activation; fatty acid chain length; PROTEIN-KINASE-C; MYOGENIC DIFFERENTIATION; GLUCOSE-TRANSPORTER; ALPHA EXPRESSION; TNF-ALPHA; PALMITATE; CERAMIDE; INTERLEUKIN-6; INHIBITION; MECHANISM;
D O I
10.1152/ajpendo.00436.2007
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Hommelberg PP, Plat J, Langen RC, Schols AM, Mensink RP. Fatty acid-induced NF-kappa B activation and insulin resistance in skeletal muscle are chain length dependent. Am J Physiol Endocrinol Metab 296: E114-E120, 2009. First published October 28, 2008; doi: 10.1152/ajpendo.00436.2007.-The saturated fatty acid (SFA) palmitate induces insulin resistance in cultured skeletal muscle cells, which may be related to NF-kappa B activation. The aim of this study was to evaluate whether other SFAs also exert these effects on skeletal muscle and whether these relate to chain length. Therefore, we incubated L6 and C2C12 skeletal muscle cells with four different fatty acids, caprylate (C8:0), laurate (C12:0), palmitate (C16:0), and stearate (C18:0), to study effects on GLUT4 translocation, deoxyglucose uptake, and NF-kappa B activation. Incubation of L6 cells with the long-chain FAs C16:0 and C18:0 reduced insulin-stimulated GLUT4 translocation and deoxyglucose uptake, whereas L6 cells incubated with the medium-chain FAs C8:0 and C12:0 remained insulin sensitive. Besides increasing NF-kappa B DNA binding activity in both L6 and C2C12 cells, C16:0 also induced NF-kappa B transcriptional activity. C18:0 showed comparable effects, whereas the SFAs with shorter chain lengths were not able to elevate NF-kappa B transcriptional activity. Collectively, these results demonstrate that SFA-induced NF-kappa B activation coincides with insulin resistance and depends on FA chain length.
引用
收藏
页码:E114 / E120
页数:7
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