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PMID: 12646246 Published · ppublish English Journal Article

Interleukin-6 gene expression is increased in insulin-resistant rat skeletal muscle following insulin stimulation.

Biochemical and biophysical research communications ·Vol. 302 ·No. 4 ·2003-03-21 ·Pages 837-40

Carey AL, Lamont B, Andrikopoulos S, Koukoulas I, Proietto J, Febbraio MA

Abstract

IL-6 expression in skeletal muscle is stimulated by contractions. We sought to examine whether hyperinsulinaemia increases IL-6 mRNA in skeletal muscle and whether any increase is modified in insulin resistant muscle. We hypothesized that intramuscular IL-6 mRNA would be increased in response to insulin, but such an affect would be unaffected by insulin resistance because the primary insulin sensitive signalling protein responsible for activating IL-6 functions normally in insulin resistant muscle. Transgenic rats over-expressing the gluconeogenic regulatory enzyme phosphoenolpyruvate carboxykinase (PEPCK) were studied. White gastrocnemius muscle samples were obtained under hyperinsulinaemic, euglycaemic clamp (4 mU kg(-1)min(-1) insulin, plasma glucose concentration 4-6 mmol L(-1)) and basal conditions in both PEPCK (basal n=4; insulin n=5) and wild-type (CON) (basal n=5; insulin n=4) rats, which were previously injected with a bolus of 2-[1-14C]deoxyglucose (2-DG) into the carotid artery. Muscle samples were assayed for 2-DG uptake and IL-6 mRNA. No differences in 2-DG uptake or IL-6 mRNA were observed when comparing groups under basal conditions. Under clamp conditions, 2-DG uptake was lower (P<0.05) in PEPCK compared with CON. Insulin stimulation in CON did not change IL-6 mRNA compared with basal levels. In contrast, there was an approximately 8-fold increase (P<0.05) in IL-6 mRNA in insulin-stimulated PEPCK compared with CON basal levels. Insulin stimulation increases IL-6 gene expression in insulin resistant, but not healthy, skeletal muscle, suggesting that IL-6 expression in skeletal muscle is sensitive to changes in insulin in circumstances of insulin resistance. It is likely that the differences observed when comparing healthy with insulin resistant muscle are due to the differential activation of insulin sensitive signalling proteins responsible for activating IL-6.

MeSH Terms
Animals Animals, Genetically Modified Blood Glucose/metabolism Deoxyglucose/metabolism Humans Insulin/pharmacology Insulin Resistance/physiology Interleukin-6/genetics,metabolism MAP Kinase Signaling System/physiology Muscle Contraction/physiology Muscle, Skeletal/drug effects,physiology Protein Serine-Threonine Kinases/genetics,metabolism RNA, Messenger/metabolism Rats
Chemicals
Blood Glucose Insulin Interleukin-6 RNA, Messenger Deoxyglucose phosphoenolpyruvate carboxylase kinase Protein Serine-Threonine Kinases
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Carey A L
Department of Physiology, The University of Melbourne, Parkville 3010, Vic., Australia.
Lamont B
Andrikopoulos S
Koukoulas I
Proietto J
Febbraio M A
Article Info
Journal
Biochemical and biophysical research communications
Abbr.
Biochem Biophys Res Commun
ISSN
0006-291X
Published
2003-03-21
Pages
837-40
Language
English
Region
United States
NLM ID
0372516
Subset
IM
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