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Downregulation of AMPK Accompanies Leucine- and Glucose-Induced Increases in Protein Synthesis and Insulin Resistance in Rat Skeletal Muscle
- Source :
- Diabetes
- Publication Year :
- 2010
- Publisher :
- American Diabetes Association, 2010.
-
Abstract
- OBJECTIVE Branched-chain amino acids, such as leucine and glucose, stimulate protein synthesis and increase the phosphorylation and activity of the mammalian target of rapamycin (mTOR) and its downstream target p70S6 kinase (p70S6K). We examined in skeletal muscle whether the effects of leucine and glucose on these parameters and on insulin resistance are mediated by the fuel-sensing enzyme AMP-activated protein kinase (AMPK). RESEARCH DESIGN AND METHODS Rat extensor digitorum longus (EDL) muscle was incubated with different concentrations of leucine and glucose with or without AMPK activators. Muscle obtained from glucose-infused rats was also used as a model. RESULTS In the EDL, incubation with 100 or 200 μmol/l leucine versus no added leucine suppressed the activity of the α2 isoform of AMPK by 50 and 70%, respectively, and caused concentration-dependent increases in protein synthesis and mTOR and p70S6K phosphorylation. Very similar changes were observed in EDL incubated with 5.5 or 25 mmol/l versus no added glucose and in muscle of rats infused with glucose in vivo. Incubation of the EDL with the higher concentrations of both leucine and glucose also caused insulin resistance, reflected by a decrease in insulin-stimulated Akt phosphorylation. Coincubation with the AMPK activators AICAR and α-lipoic acid substantially prevented all of those changes and increased the phosphorylation of specific sites of mTOR inhibitors raptor and tuberous sclerosis complex 2 (TSC2). In contrast, decreases in AMPK activity induced by leucine and glucose were not associated with a decrease in raptor or TSC2 phosphorylation. CONCLUSIONS The results indicate that both leucine and glucose modulate protein synthesis and mTOR/p70S6 and insulin signaling in skeletal muscle by a common mechanism. They also suggest that the effects of both molecules are associated with a decrease in AMPK activity and that AMPK activation prevents them.
- Subjects :
- medicine.medical_specialty
Endocrinology, Diabetes and Metabolism
Down-Regulation
AMP-Activated Protein Kinases
Protein Serine-Threonine Kinases
Insulin resistance
AMP-activated protein kinase
Downregulation and upregulation
Leucine
Internal medicine
Internal Medicine
medicine
Animals
Phosphorylation
Muscle, Skeletal
Pyruvates
Dose-Response Relationship, Drug
biology
TOR Serine-Threonine Kinases
Adenylate Kinase
Intracellular Signaling Peptides and Proteins
Ribosomal Protein S6 Kinases, 70-kDa
Skeletal muscle
AMPK
Ribonucleotides
Aminoimidazole Carboxamide
Phosphoproteins
medicine.disease
Rats
Kinetics
Insulin receptor
Metabolism
Glucose
medicine.anatomical_structure
Endocrinology
Lactates
biology.protein
Insulin Resistance
Carrier Proteins
Subjects
Details
- ISSN :
- 1939327X and 00121797
- Volume :
- 59
- Database :
- OpenAIRE
- Journal :
- Diabetes
- Accession number :
- edsair.doi.dedup.....6116806723c90731eb4689472d869be1