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PMID: 15165992 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

AMP kinase is not required for the GLUT4 response to exercise and denervation in skeletal muscle.

American journal of physiology. Endocrinology and metabolism ·Vol. 287 ·No. 4 ·2004-10-00 ·Pages E739-43

Holmes BF, Lang DB, Birnbaum MJ, Mu J, Dohm GL

Abstract

An acute bout of exercise increases muscle GLUT4 mRNA in mice, and denervation decreases GLUT4 mRNA. AMP-activated protein kinase (AMPK) activity in skeletal muscle is also increased by exercise, and GLUT4 mRNA is increased in mouse skeletal muscle after treatment with AMPK activator 5-aminoimidazole-4-carboxamide-1-beta-D-ribofuranoside(AICAR). These findings suggest that AMPK activation might be responsible for the increase in GLUT4 mRNA expression in response to exercise. To investigate the role of AMPK in GLUT4 regulation in response to exercise and denervation, transgenic mice with a mutated AMPK alpha-subunit (dominant negative; AMPK-DN) were studied. GLUT4 did not increase in AMPK-DN mice that were treated with AICAR, demonstrating that muscle AMPK is inactive. Exercise (two 3-h bouts of treadmill running separated by 1 h of rest) increased GLUT4 mRNA in both wild-type and AMPK-DN mice. Likewise, denervation decreased GLUT4 mRNA in both wild-type and AMPK-DN mice. GLUT4 mRNA was also increased by AICAR treatment in both the innervated and denervated muscles. These data demonstrate that AMPK is not required for the response of GLUT4 mRNA to exercise and denervation.

MeSH Terms
Aminoimidazole Carboxamide/analogs & derivatives,pharmacology Animals Blotting, Northern Catalase/biosynthesis Cyclic AMP-Dependent Protein Kinases/genetics,physiology Enzyme Activators/pharmacology Glucose Transporter Type 4 Glyceraldehyde-3-Phosphate Dehydrogenases/biosynthesis Mice Mice, Transgenic Monosaccharide Transport Proteins/biosynthesis Muscle Denervation Muscle Proteins/biosynthesis Muscle, Skeletal/metabolism Nuclease Protection Assays Physical Exertion/physiology RNA, Messenger/analysis,biosynthesis Reverse Transcriptase Polymerase Chain Reaction Ribonucleotides/pharmacology
Chemicals
Enzyme Activators Glucose Transporter Type 4 Monosaccharide Transport Proteins Muscle Proteins RNA, Messenger Ribonucleotides Slc2a4 protein, mouse Aminoimidazole Carboxamide Catalase Glyceraldehyde-3-Phosphate Dehydrogenases Cyclic AMP-Dependent Protein Kinases AICA ribonucleotide
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Holmes Burton F
East Carolina University, Greenville, NC 27858, USA.
Lang David B
Birnbaum Morris J
Mu James
Dohm G Lynis
Article Info
Journal
American journal of physiology. Endocrinology and metabolism
Abbr.
Am J Physiol Endocrinol Metab
ISSN
0193-1849
Published
2004-10-00
Epub
2004-00-27
Pages
E739-43
Language
English
Region
United States
NLM ID
100901226
Subset
IM
Grants
NIDDK NIH HHS · R01-DK-38416 · United States
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