Fatty acid-induced NF-{kappa}B activation and insulin resistance in skeletal muscle are chain length dependent.

    Research output: Contribution to journalArticleAcademicpeer-review

    Abstract

    The saturated fatty acid (SFA) palmitate (C16:0) induces insulin resistance in cultured skeletal muscle cells, which may be related to NF-kappaB activation. The aim of this study was to evaluate if other SFA 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-kappaB activation. Incubation of L6 cells with the long-chain FA C16:0 and C18:0 resulted in a reduced insulin-stimulated GLUT4 translocation and deoxyglucose uptake, while L6 cells incubated with the medium-chain FA C8:0 and C12:0 remained insulin sensitive. Besides increasing NF-kappaB DNA binding activity in both L6 and C2C12 cells, C16:0 also induced NF-kappaB transcriptional activity. C18:0 showed comparable effects, while the SFA with shorter chain lengths were not able to elevate NF-kappaB transcriptional activity. Collectively, these results demonstrate that SFA-induced NF-kappaB activation coincides with insulin resistance and depends on FA chain length. Key words: GLUT4 translocation, NF-kappaB activation, fatty acid chain length, insulin resistance, skeletal muscle.
    Original languageEnglish
    Pages (from-to)E114-E120
    JournalAmerican Journal of Physiology : Endocrinology and Metabolism
    Volume296
    Issue number1
    DOIs
    Publication statusPublished - 1 Jan 2009

    Cite this