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This version published online on October 29, 2009
Journal of Clinical Endocrinology & Metabolism , doi:10.1210/jc.2009-1147
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Submitted on May 28, 2009
Accepted on September 29, 2009

Dissociation between Skeletal Muscle Inhibitor-{kappa}B Kinase/Nuclear Factor-{kappa}B Pathway Activity and Insulin Sensitivity in Nondiabetic Twins

Martin Friedrichsen*, Rasmus Ribel-Madsen, Jørgen Wojtaszewski, Louise Grunnet, Erik A. Richter, Nils Billestrup, Thorkil Ploug, Allan Vaag, and Pernille Poulsen

Steno Diabetes Center (M.F., R.R.-M., L.G., N.B., A.V., P.P.), DK-2820 Gentofte, Denmark; Section of Systems Biology Research (M.F., T.P.), Department of Biomedical Sciences, The Panum Institute, University of Copenhagen, DK-2200 Copenhagen, Denmark; Copenhagen Muscle Research Centre (J.W., E.A.R.), Department of Exercise and Sport Sciences, University of Copenhagen, DK-2100 Copenhagen, Denmark; and Department of Clinical Sciences (A.V.), Lund University, Malmö University Hospital, S-205 02 Malmö, Sweden

* To whom correspondence should be addressed. E-mail: mfrc{at}steno.dk.

Context: Several studies suggest a link between increased activity of the inflammatory inhibitor-{kappa}B kinase/nuclear factor-{kappa}B (IKK/NF-{kappa}B) pathway in skeletal muscle and insulin resistance.

Objective: We aimed to study the regulation of skeletal muscle IKK/NF-{kappa}B pathway activity as well as the association with glucose metabolism and skeletal muscle insulin signaling.

Methods: The study population included a metabolically well-characterized cohort of young and elderly predominantly nondiabetic twins (n = 181). Inhibitor-{kappa}B{beta} (I{kappa}B{beta}) protein levels are negatively associated with IKK/NF-{kappa}B pathway activity and were used to evaluate pathway activity with p65 levels included as loading control. This indirect measure for IKK/NF-{kappa}B pathway activity was validated by a p65 binding assay.

Results: Evaluating the effects of heritability, age, sex, obesity, aerobic capacity, and several hormonal factors (eg insulin and TNF-{alpha}), only sex and age were significant predictors of I{kappa}B{beta} to p65 ratio (28% decreased ratio in the elderly, P < 0.01, and 49% increased in males P < 0.01). I{kappa}B{beta} to p65 ratio was unrelated to peripheral insulin sensitivity (P = 0.51) and in accordance with this also unrelated to proximal insulin signaling (P = 0.81). Although no association was seen with plasma glucose after oral glucose challenge, there was a tendency for lower I{kappa}B{beta} to p65 ratio (adjusted for age and sex) in subjects with impaired as opposed to normal glucose tolerance (P = 0.055).

Conclusions: Altogether the subtle elevated IKK/NF-{kappa}B pathway activity seen in glucose-intolerant subjects suggests that IKK/NF-{kappa}B pathway activation may be secondary to impaired glucose tolerance and that skeletal muscle IKK/NF-{kappa}B pathway activity is unlikely to play any major role in the control of skeletal muscle insulin action in nondiabetic subjects.







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