Transcriptional Metabolic Inflexibility in Skeletal Muscle Among Individuals With Increasing Insulin Resistance

• Published in: Obesity (Silver Spring, Md.) Md.), 2011-11, Vol.19 (11), p.2158-2166
• Main Authors: Jans, Anneke, Sparks, Lauren M., Hees, Anneke M.J., Gjelstad, Ingrid M.F., Tierney, Audrey C., Risérus, Ulf, Drevon, Christian A., Roche, Helen M., Schrauwen, Patrick, Blaak, Ellen E.
• Format: Article
• Language: English
• Subjects: Acetyl-CoA Carboxylase - metabolism; Adult; Aged; Carnitine O-Palmitoyltransferase - genetics; Carnitine O-Palmitoyltransferase - metabolism; Diacylglycerol O-Acyltransferase - metabolism; Fatty Acids - metabolism; Female; Gene Expression Regulation; Heat-Shock Proteins - genetics; Heat-Shock Proteins - metabolism; Humans; Hyperinsulinism - genetics; Hyperinsulinism - metabolism; Insulin - metabolism; Insulin Resistance; Lipid Metabolism; Lipoprotein Lipase - metabolism; Male; Metabolic Syndrome - genetics; Metabolic Syndrome - metabolism; Middle Aged; Muscle, Skeletal - metabolism; Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha; PPAR alpha - genetics; PPAR alpha - metabolism; RNA, Messenger; Sterol Regulatory Element Binding Protein 1 - genetics; Sterol Regulatory Element Binding Protein 1 - metabolism; Transcription Factors - genetics; Transcription Factors - metabolism
• ISSN: 1930-7381; 1930-739X; 1930-739X
• DOI: 10.1038/oby.2011.149

Disturbances in skeletal muscle lipid metabolism may play an important role in development of insulin resistance (IR). The aim was to investigate transcriptional control of skeletal muscle fatty acid (FA) metabolism in individuals with the metabolic syndrome (MetS) with varying degrees of insulin sensitivity (SI). 122 individuals with MetS (NCEP‐ATP III criteria) at age 35–70 years, BMI 27–38 kg/m2 were studied (subgroup EU‐LIPGENE study). Individuals were divided into quartiles of SI measured during a frequently sampled insulin modified intravenous glucose tolerance test. Skeletal muscle normalized mRNA expression levels of genes important in skeletal muscle FA handling were analyzed with quantitative real‐time PCR. The expression of sterol regulatory element binding protein 1c (SREBP1c), acetyl‐CoA carboxylase 2 (ACC2), diacylglycerol acyltransferase (DGAT1), and nuclear respiration factor (NRF) was higher in the lowest two quartiles of SI (50th). Interestingly, peroxisome proliferator‐activated receptor coactivator 1α (PGC1α), peroxisome proliferator‐activated receptor α (PPARα), and muscle carnitine palmitoyl transferase 1b (mCPT1), important for oxidative metabolism, showed a complex mRNA expression profile; levels were lower in both the most “insulin sensitive” (IS) as well as the most “IR” individuals. Lipoprotein lipase (LPL) mRNA was reduced in the lowest quartile of SI. Enhanced gene expression of SREBP1c and ACC2 in the IR state suggests a tendency towards FA storage rather than oxidation. From the lower expression of PGC1α, PPARα, and mCPT1 in both the most “IS” as well as the most “IR” individuals, it may be speculated that “IS” subjects do not need to upregulate these genes to have a normal FA oxidation, whereas the most “IR” individuals are inflexible in upregulating these genes.