help button home button Endocrine Society Endocrinology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH

This version published online on February 2, 2006
Endocrinology, doi:10.1210/en.2005-0898
A more recent version of this article appeared on May 1, 2006
This Article
Right arrow Author Manuscript (PDF)
Right arrow All Versions of this Article:
147/5/2432    most recent
Author Manuscript (PDF)
Right arrow Purchase Article
Right arrow View Shopping Cart
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Request Copyright Permission
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Andreelli, F.
Right arrow Articles by Viollet, B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Andreelli, F.
Right arrow Articles by Viollet, B.

Submitted on July 19, 2005
Accepted on January 26, 2006

Liver AMPKalpha2 catalytic subunit is a key target for the control of hepatic glucose production by adiponectin and leptin but not by insulin

Fabrizio Andreelli, Marc Foretz, Claude Knauf, Patrice D. Cani, Christophe Perrin, Miguel A. Iglesias, Bruno Pillot, André Bado, François Tronche, Gilles Mithieux, Sophie Vaulont, Rémy Burcelin*, and Benoit Viollet

Institut National de la Santé et de la Recherche Médicale Unité 567, Centre National de la Recherche Scientifique Unité Mixte de Recherche 8104, Université René Descartes Paris 5, Institut Fédératif de Recherche 116 Alfred Jost, Institut Cochin, Department of Genetic, Development and Molecular Pathology, Paris, France; Unité Mixte de Recherche 5018, Centre National de la Recherche Scientifique, Université Paul Sabatier and Institut Fédératif de Recherche 31, Hôpital Rangueil, Toulouse, France; Institut National de la Sante et de la Recherche Medicale, Unité 449, 69372 Lyon, France; Institut National de la Santé et de la Recherche Médicale Unité 683, Institut Fédératif de Recherche 02 Claude Bernard, Faculte de Médecine Xavier Bichat, Paris, France; Collège de France, Centre National de la Recherche Scientifique Formation de Recherche en Evolution 2401, Paris, France

* To whom correspondence should be addressed. E-mail: burcelin{at}toulouse.inserm.fr.

The AMP-activated kinase (AMPK) is a serine threonine kinase which functions as a fuel sensor to regulate energy balance at both cellular and whole body levels. Here, we studied how hepatic AMPK{alpha}2 isoform affects hepatic glucose production and peripheral glucose uptake in vivo. We generated mice deleted for the AMPK{alpha}2 gene specifically in the liver (liver{alpha}2KO). Liver{alpha}2KO mice were glucose intolerant and hyperglycemic in the fasted state. Hyperglycemia was associated with a 50% higher endogenous glucose production (EGP) than in controls as assessed in vivo. We then investigated whether this increased glucose production was sensitive to insulin. Insulin, when infused at a rate inducing physiological hyperinsulinemia, totally inhibited EGP in liver{alpha}2KO mice, showing that they had normal insulin sensitivity. This was confirmed in vivo by normal insulin-induced phosphorylation of Akt and transcriptional regulation of the phosphoenolpyruvate carboxykinase, glucose-6 phosphatase and pyruvate kinase in liver during the fasted/fed transition. Leptin and adiponectin regulate hepatic glucose production, so we then infused these adipokines into liver{alpha}2KO mice. Neither of these adipokines regulated hepatic glucose production in mice lacking hepatic AMPK{alpha}2, whereas both did so in control mice. In conclusion, we show that the hepatic AMPK{alpha}2 isoform is essential for suppressing hepatic glucose production and maintaining fasting blood glucose levels in the physiological range. We also demonstrate that regulation of hepatic glucose production by leptin and adiponectin, but not insulin, requires hepatic AMPK{alpha}2 activity.




This article has been cited by other articles:


Home page
Mol. Endocrinol.Home page
M. Lu, Q. Tang, J. M. Olefsky, P. L. Mellon, and N. J. G. Webster
Adiponectin Activates Adenosine Monophosphate-Activated Protein Kinase and Decreases Luteinizing Hormone Secretion in L{beta}T2 Gonadotropes
Mol. Endocrinol., March 1, 2008; 22(3): 760 - 771.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
N. L. Brooks, C. M. Trent, C. F. Raetzsch, K. Flurkey, G. Boysen, M. T. Perfetti, Y.-C. Jeong, S. Klebanov, K. B. Patel, V. R. Khodush, et al.
Low Utilization of Circulating Glucose after Food Withdrawal in Snell Dwarf Mice
J. Biol. Chem., November 30, 2007; 282(48): 35069 - 35077.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
M. J. Sanders, Z. S. Ali, B. D. Hegarty, R. Heath, M. A. Snowden, and D. Carling
Defining the Mechanism of Activation of AMP-activated Protein Kinase by the Small Molecule A-769662, a Member of the Thienopyridone Family
J. Biol. Chem., November 9, 2007; 282(45): 32539 - 32548.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
A. Suzuki, S. Okamoto, S. Lee, K. Saito, T. Shiuchi, and Y. Minokoshi
Leptin Stimulates Fatty Acid Oxidation and Peroxisome Proliferator-Activated Receptor {alpha} Gene Expression in Mouse C2C12 Myoblasts by Changing the Subcellular Localization of the {alpha}2 Form of AMP-Activated Protein Kinase
Mol. Cell. Biol., June 15, 2007; 27(12): 4317 - 4327.
[Abstract] [Full Text] [PDF]


Home page
DiabetesHome page
E. Lin, L. S. Phillips, T. R. Ziegler, B. Schmotzer, K. Wu, L. H. Gu, L. Khaitan, S. A. Lynch, W. E. Torres, C. D. Smith, et al.
Increases in Adiponectin Predict Improved Liver, but Not Peripheral, Insulin Sensitivity in Severely Obese Women During Weight Loss
Diabetes, March 1, 2007; 56(3): 735 - 742.
[Abstract] [Full Text] [PDF]


Home page
Circ. Res.Home page
M. C. Towler and D. G. Hardie
AMP-Activated Protein Kinase in Metabolic Control and Insulin Signaling
Circ. Res., February 16, 2007; 100(3): 328 - 341.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
S. P. Berasi, C. Huard, D. Li, H. H. Shih, Y. Sun, W. Zhong, J. E. Paulsen, E. L. Brown, R. E. Gimeno, and R. V. Martinez
Inhibition of Gluconeogenesis through Transcriptional Activation of EGR1 and DUSP4 by AMP-activated Kinase
J. Biol. Chem., September 15, 2006; 281(37): 27167 - 27177.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
B. Viollet, M. Foretz, B. Guigas, S. Horman, R. Dentin, L. Bertrand, L. Hue, and F. Andreelli
Activation of AMP-activated protein kinase in the liver: a new strategy for the management of metabolic hepatic disorders
J. Physiol., July 1, 2006; 574(1): 41 - 53.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
Endocrinology Endocrine Reviews J. Clin. End. & Metab.
Molecular Endocrinology Recent Prog. Horm. Res. All Endocrine Journals
Copyright © 2006 by The Endocrine Society