Physiological role of AMP-activated protein kinase (AMPK): insights from knockout mouse models. (1st February 2003)
- Record Type:
- Journal Article
- Title:
- Physiological role of AMP-activated protein kinase (AMPK): insights from knockout mouse models. (1st February 2003)
- Main Title:
- Physiological role of AMP-activated protein kinase (AMPK): insights from knockout mouse models
- Authors:
- Viollet, B.
Andreelli, F.
Jørgensen, S.B.
Perrin, C.
Flamez, D.
Mu, J.
Wojtaszewski, J.F.P.
Schuit, F.C.
Birnbaum, M.
Richter, E.
Burcelin, R.
Vaulont, S. - Abstract:
- Abstract : AMP-activated protein kinase (AMPK) is viewed as a fuel sensor for glucose and lipid metabolism. To understand better the physiological role of the catalytic AMPK subunit isoforms, we generated two knockout mouse models with the α1 (AMPKα1 −/− ) and α2 (AMPKα2 −/− ) catalytic subunit genes deleted. No defect in glucose homoeostasis was observed in AMPKα1 −/− mice. On the other hand, AMPKα2 −/− mice presented high plasma glucose levels and low plasma insulin concentrations in the fed period and during the glucose tolerance test. Nevertheless, in isolated AMPKα2 −/− pancreatic islets, glucose-stimulated insulin secretion was not affected. Surprisingly, AMPKα2 −/− mice were insulin-resistant and had reduced muscle glycogen synthesis as assessed in vivo by the hyperinsulinaemic euglycaemic clamp procedure. Reduction of insulin sensitivity and glycogen synthesis were not dependent on the lack of AMPK in skeletal muscle, since mice expressing a dominant inhibitory mutant of AMPK in skeletal muscle were not affected and since insulin-stimulated glucose transport in incubated muscles in vitro was normal in AMPKα2 −/− muscles. Furthermore, AMPKα2 −/− mice have a higher sympathetic tone, as shown by increased catecholamine urinary excretion. Increased adrenergic tone could explain both decreased insulin secretion and insulin resistance observed in vivo in AMPKα2 −/− mice. We suggest that the α2 catalytic subunit of AMPK plays a major role as a fuel sensor by modulating theAbstract : AMP-activated protein kinase (AMPK) is viewed as a fuel sensor for glucose and lipid metabolism. To understand better the physiological role of the catalytic AMPK subunit isoforms, we generated two knockout mouse models with the α1 (AMPKα1 −/− ) and α2 (AMPKα2 −/− ) catalytic subunit genes deleted. No defect in glucose homoeostasis was observed in AMPKα1 −/− mice. On the other hand, AMPKα2 −/− mice presented high plasma glucose levels and low plasma insulin concentrations in the fed period and during the glucose tolerance test. Nevertheless, in isolated AMPKα2 −/− pancreatic islets, glucose-stimulated insulin secretion was not affected. Surprisingly, AMPKα2 −/− mice were insulin-resistant and had reduced muscle glycogen synthesis as assessed in vivo by the hyperinsulinaemic euglycaemic clamp procedure. Reduction of insulin sensitivity and glycogen synthesis were not dependent on the lack of AMPK in skeletal muscle, since mice expressing a dominant inhibitory mutant of AMPK in skeletal muscle were not affected and since insulin-stimulated glucose transport in incubated muscles in vitro was normal in AMPKα2 −/− muscles. Furthermore, AMPKα2 −/− mice have a higher sympathetic tone, as shown by increased catecholamine urinary excretion. Increased adrenergic tone could explain both decreased insulin secretion and insulin resistance observed in vivo in AMPKα2 −/− mice. We suggest that the α2 catalytic subunit of AMPK plays a major role as a fuel sensor by modulating the activity of the autonomous nervous system in vivo . … (more)
- Is Part Of:
- Biochemical Society transactions. Volume 31:Number 1(2003)
- Journal:
- Biochemical Society transactions
- Issue:
- Volume 31:Number 1(2003)
- Issue Display:
- Volume 31, Issue 1 (2003)
- Year:
- 2003
- Volume:
- 31
- Issue:
- 1
- Issue Sort Value:
- 2003-0031-0001-0000
- Page Start:
- 216
- Page End:
- 219
- Publication Date:
- 2003-02-01
- Subjects:
- glucose metabolism -- insulin resistance
Biochemistry -- Congresses
572 - Journal URLs:
- https://portlandpress.com/biochemsoctrans ↗
- DOI:
- 10.1042/bst0310216 ↗
- Languages:
- English
- ISSNs:
- 0300-5127
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library HMNTS - ELD Digital store
- Ingest File:
- 16098.xml