Role of 5′ AMP-activated protein kinase in glycogen synthase activity and glucose utilization: Insights from patients from McArdle's disease

Jakob N. Nielsen, Jørgen F P Wojtaszewski, Ronald G. Haller, D. Grahame Hardie, Bruce E. Kemp, Erik A. Richter, John Vissing

Research output: Contribution to journalArticle

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Abstract

It has been suggested that 5′AMP-activated protein kinase (AMPK) is involved in the regulation of glucose and glycogen metabolism in skeletal muscle. We used patients with chronic high muscle glycogen stores and deficient glycogenolysis (McArdle's disease) as a model to address this issue. Six McArdle patients were compared with control subjects during exercise. Muscle α2AMPK activity increased in McArdle patients (from 1.3 ± 0.2 to 1.9 ± 0.2 pmol min-1 mg-1, P = 0.05) but not in control subjects (from 1.0 ± 0.1 to 1.3 ± 0.3 pmol min-1 mg-1). Exercise-induced phosphorylation of the in vivo AMPK substrate acetyl CoA carboxylase (ACCβ; Ser221) was higher (P < 0.0 1) in McArdle patients than in control subjects (18 ± 3 vs. 10 ± 1 arbitrary units). Exercise-induced whole-body glucose utilization was also higher in McArdle patients than in control subjects (P < 0.05). No correlation between individual AMPK or ACCβ values and glucose utilization was observed. Glycogen synthase (GS) activity was decreased in McArdle patients from 11 ± 1.3 to 5 ± 1.2% (P < 0.05) and increased in control subjects from 19 ± 1.6 to 23 ± 2.3% (P < 0.05) in response to exercise. This was not associated with activity changes of GS kinase 3 or protein phosphatase 1, but the changes in GS activity could be due to changes in activity of AMPK or protein kinase A (PKA) as a negative correlation between either ACCβ phosphorylation (Ser221) or plasma adrenaline and GS activity was observed. These findings suggest that GS activity is increased by glycogen breakdown and decreased by AMPK and possibly PKA activation and that the resultant GS activity depends on the relative strengths of the various stimuli. Furthermore, AMPK may be involved in the regulation of glucose utilization during exercise in humans, although the lack of correlation between individual AMPK activity or ACCβ phosphorylation (Ser221) values and individual glucose utilization during exercise implies that AMPK may not be an essential regulator.

Original languageEnglish (US)
Pages (from-to)979-989
Number of pages11
JournalJournal of Physiology
Volume541
Issue number3
DOIs
StatePublished - Jun 15 2002

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Glycogen Storage Disease Type V
Glycogen Synthase
AMP-Activated Protein Kinases
Glucose
Exercise
Glycogen
Phosphorylation
Cyclic AMP-Dependent Protein Kinases
Glycogen Synthase Kinase 3
Protein Phosphatase 1
Glycogenolysis
Acetyl-CoA Carboxylase
Muscles
Protein Kinases
Epinephrine
Skeletal Muscle

ASJC Scopus subject areas

  • Physiology

Cite this

Role of 5′ AMP-activated protein kinase in glycogen synthase activity and glucose utilization : Insights from patients from McArdle's disease. / Nielsen, Jakob N.; Wojtaszewski, Jørgen F P; Haller, Ronald G.; Grahame Hardie, D.; Kemp, Bruce E.; Richter, Erik A.; Vissing, John.

In: Journal of Physiology, Vol. 541, No. 3, 15.06.2002, p. 979-989.

Research output: Contribution to journalArticle

Nielsen, Jakob N. ; Wojtaszewski, Jørgen F P ; Haller, Ronald G. ; Grahame Hardie, D. ; Kemp, Bruce E. ; Richter, Erik A. ; Vissing, John. / Role of 5′ AMP-activated protein kinase in glycogen synthase activity and glucose utilization : Insights from patients from McArdle's disease. In: Journal of Physiology. 2002 ; Vol. 541, No. 3. pp. 979-989.
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