Aging-Associated Reductions in AMP-Activated Protein Kinase Activity and Mitochondrial Biogenesis

Richard M. Reznick(Howard Hughes Medical Institute), Haihong Zong(Yale University), Ji Li(Yale University), Katsutaro Morino(Howard Hughes Medical Institute), Irene K. Moore(Howard Hughes Medical Institute), Hannah J. Yu(Yale University), Zhen-Xiang Liu(Howard Hughes Medical Institute), Jianying Dong(Yale University), Kirsty J. Mustard(University of Dundee), Simon A. Hawley(University of Dundee), Douglas E. Befroy(Yale University), Marc Pypaert(Yale University), D. Grahame Hardie(University of Dundee), Lawrence H. Young(Yale University), Gerald I. Shulman(Howard Hughes Medical Institute)
Cell Metabolism
February 1, 2007
Cited by 535Open Access
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Abstract

Recent studies have demonstrated a strong relationship between aging-associated reductions in mitochondrial function, dysregulated intracellular lipid metabolism, and insulin resistance. Given the important role of the AMP-activated protein kinase (AMPK) in the regulation of fat oxidation and mitochondrial biogenesis, we examined AMPK activity in young and old rats and found that acute stimulation of AMPK-alpha(2) activity by 5'-aminoimidazole-4-carboxamide-1-beta-D-ribofuranoside (AICAR) and exercise was blunted in skeletal muscle of old rats. Furthermore, mitochondrial biogenesis in response to chronic activation of AMPK with beta-guanidinopropionic acid (beta-GPA) feeding was also diminished in old rats. These results suggest that aging-associated reductions in AMPK activity may be an important contributing factor in the reduced mitochondrial function and dysregulated intracellular lipid metabolism associated with aging.


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