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Role of 5′AMP‐activated protein kinase in glycogen synthase activity and glucose utilization: insights from patients with McArdle's disease
Author(s) -
Nielsen Jakob N.,
Wojtaszewski Jørgen F. P.,
Haller Ronald G.,
Hardie D. Grahame,
Kemp Bruce E.,
Richter Erik A.,
Vissing John
Publication year - 2002
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1113/jphysiol.2002.018044
Subject(s) - medicine , ampk , endocrinology , glycogenolysis , glycogen , protein kinase a , glycogen synthase , amp activated protein kinase , skeletal muscle , phosphorylation , acetyl coa carboxylase , phosphatase , glucose uptake , chemistry , enzyme , pyruvate carboxylase , biochemistry , insulin
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; Ser 221 ) was higher ( P < 0.01 ) 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 (Ser 221 ) 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 (Ser 221 ) values and individual glucose utilization during exercise implies that AMPK may not be an essential regulator.