The Ancient Drug Salicylate Directly Activates AMP-Activated Protein Kinase

Simon A. Hawley(University of Dundee), Morgan D. Fullerton(McMaster University), Fiona A. Ross(University of Dundee), Jonathan D. Schertzer(McMaster University), Cyrille Chevtzoff(University of Dundee), Katherine J. Walker(University of Dundee), Mark Peggie(University of Dundee), Darya Zibrova(University of Dundee), Kevin A. Green(University of Dundee), Kirsty J. Mustard(University of Dundee), Bruce E. Kemp(The University of Melbourne), Kei Sakamoto(University of Dundee), Gregory R. Steinberg(St Vincents Institute of Medical Research), D. Grahame Hardie(University of Dundee)
Science
April 20, 2012
Cited by 732

Abstract

Salicylate, a plant product, has been in medicinal use since ancient times. More recently, it has been replaced by synthetic derivatives such as aspirin and salsalate, both of which are rapidly broken down to salicylate in vivo. At concentrations reached in plasma after administration of salsalate or of aspirin at high doses, salicylate activates adenosine monophosphate-activated protein kinase (AMPK), a central regulator of cell growth and metabolism. Salicylate binds at the same site as the synthetic activator A-769662 to cause allosteric activation and inhibition of dephosphorylation of the activating phosphorylation site, threonine-172. In AMPK knockout mice, effects of salicylate to increase fat utilization and to lower plasma fatty acids in vivo were lost. Our results suggest that AMPK activation could explain some beneficial effects of salsalate and aspirin in humans.


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