• Title of article

    AMPK and PPARδ Agonists Are Exercise Mimetics

  • Author/Authors

    Vihang A. Narkar، نويسنده , , Michael Downes، نويسنده , , Ruth T. Yu، نويسنده , , Emi Embler، نويسنده , , Yong-Xu Wang، نويسنده , , Ester Banayo، نويسنده , , Maria M. Mihaylova، نويسنده , , Michael C. Nelson، نويسنده , , Yuhua Zou، نويسنده , , Henry Juguilon، نويسنده , , Heonjoong Kang، نويسنده , , Reuben J. Shaw، نويسنده , , Ronald M. Evans، نويسنده ,

  • Issue Information
    هفته نامه با شماره پیاپی سال 2008
  • Pages
    11
  • From page
    405
  • To page
    415
  • Abstract
    The benefits of endurance exercise on general health make it desirable to identify orally active agents that would mimic or potentiate the effects of exercise to treat metabolic diseases. Although certain natural compounds, such as reseveratrol, have endurance-enhancing activities, their exact metabolic targets remain elusive. We therefore tested the effect of pathway-specific drugs on endurance capacities of mice in a treadmill running test. We found that PPARβ/δ agonist and exercise training synergistically increase oxidative myofibers and running endurance in adult mice. Because training activates AMPK and PGC1α, we then tested whether the orally active AMPK agonist AICAR might be sufficient to overcome the exercise requirement. Unexpectedly, even in sedentary mice, 4 weeks of AICAR treatment alone induced metabolic genes and enhanced running endurance by 44%. These results demonstrate that AMPK-PPARδ pathway can be targeted by orally active drugs to enhance training adaptation or even to increase endurance without exercise.
  • Journal title
    CELL
  • Serial Year
    2008
  • Journal title
    CELL
  • Record number

    1019359