Ivakine Evgueni A, Cohn Ronald D
* The Hospital for Sick Children, 555 University Avenue, Toronto, Ontario, Canada M5G 1X8.
Exp Physiol. 2014 Apr;99(4):632-7. doi: 10.1113/expphysiol.2013.074344. Epub 2014 Jan 17.
Muscle disuse and starvation are often associated with a catabolic response leading to a dramatic loss of skeletal muscle mass. Hibernating animals represent a unique situation where muscle mass is maintained despite prolonged periods of immobilization and lack of nutrition. We analysed the molecular pathways upregulated during hibernation in an obligate hibernator, the 13-lined ground squirrel (Ictidomys tridecemlineatus). Although Akt has an established role in skeletal muscle maintenance, we found that activated Akt was decreased in skeletal muscle of hibernating squirrels. Another serine-threonine kinase, serum- and glucocorticoid-regulated kinase 1 (SGK1), was upregulated during hibernation and contributed to protection from loss of muscle mass via downregulation of proteolysis and autophagy and via an increase in protein synthesis. We extended our observations to non-hibernating animals and demonstrated that SGK1-null mice developed muscle atrophy. These mice displayed an exaggerated response to immobilization and starvation. Furthermore, SGK1 overexpression prevented immobilization-induced muscle atrophy. Taken together, our results identify SGK1 as a novel therapeutic target to combat skeletal muscle loss in acquired and inherited forms of muscle atrophy.
肌肉废用和饥饿通常与分解代谢反应相关,导致骨骼肌质量急剧下降。冬眠动物呈现出一种独特的情况,尽管长时间不活动且缺乏营养,但肌肉质量仍得以维持。我们分析了专性冬眠动物十三条纹地松鼠(Ictidomys tridecemlineatus)在冬眠期间上调的分子途径。尽管Akt在骨骼肌维持中具有既定作用,但我们发现冬眠松鼠的骨骼肌中活化的Akt减少。另一种丝氨酸 - 苏氨酸激酶,即血清和糖皮质激素调节激酶1(SGK1),在冬眠期间上调,并通过下调蛋白水解和自噬以及增加蛋白质合成,有助于防止肌肉质量损失。我们将观察结果扩展到非冬眠动物,并证明SGK1基因敲除小鼠会发生肌肉萎缩。这些小鼠对固定和饥饿表现出过度反应。此外,SGK1过表达可预防固定诱导的肌肉萎缩。综上所述,我们的结果表明SGK1是对抗获得性和遗传性肌肉萎缩形式中骨骼肌损失的新型治疗靶点。