Narkar Vihang A, Downes Michael, Yu Ruth T, Embler Emi, Wang Yong-Xu, Banayo Ester, Mihaylova Maria M, Nelson Michael C, Zou Yuhua, Juguilon Henry, Kang Heonjoong, Shaw Reuben J, Evans Ronald M
Gene Expression Laboratory, Salk Institute, La Jolla, CA 92037, USA.
Cell. 2008 Aug 8;134(3):405-15. doi: 10.1016/j.cell.2008.06.051. Epub 2008 Jul 31.
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 PPARbeta/delta agonist and exercise training synergistically increase oxidative myofibers and running endurance in adult mice. Because training activates AMPK and PGC1alpha, 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-PPARdelta pathway can be targeted by orally active drugs to enhance training adaptation or even to increase endurance without exercise.
耐力运动对总体健康有益,因此确定能够模拟或增强运动效果以治疗代谢性疾病的口服活性药物很有必要。尽管某些天然化合物,如白藜芦醇,具有增强耐力的活性,但其确切的代谢靶点仍不清楚。因此,我们在跑步机跑步试验中测试了特定通路药物对小鼠耐力的影响。我们发现,PPARβ/δ激动剂与运动训练协同增加成年小鼠的氧化型肌纤维和跑步耐力。由于训练会激活AMPK和PGC1α,于是我们测试了口服活性AMPK激动剂AICAR是否足以满足运动需求。出乎意料的是,即使是久坐不动的小鼠,单独进行4周的AICAR治疗也能诱导代谢基因,并使跑步耐力提高44%。这些结果表明,AMPK-PPARδ通路可以被口服活性药物靶向,以增强训练适应性,甚至在不运动的情况下增加耐力。