Dreyer Hans C, Drummond Micah J, Glynn Erin L, Fujita Satoshi, Chinkes David L, Volpi Elena, Rasmussen Blake B
Univ. of Texas Medical Branch, Dept. of Physical Therapy, 301 Univ. Blvd., Galveston, TX 77555-1144, USA.
J Appl Physiol (1985). 2008 Dec;105(6):1967-74. doi: 10.1152/japplphysiol.90562.2008. Epub 2008 Oct 9.
Akt substrate of 160 kDa (AS160/TBC1D4) is associated with insulin and contraction-mediated glucose uptake. Human skeletal muscle AS160 phosphorylation is increased during aerobic exercise but not immediately following resistance exercise. It is not known whether AS160 phosphorylation is altered during recovery from resistance exercise. Therefore, we hypothesized that muscle AS160/TBC1D4 phosphorylation and glucose uptake across the leg would be increased during recovery following resistance exercise. We studied 9 male subjects before, during, and for 2 h of postexercise recovery. We utilized femoral catheterizations and muscle biopsies in combination with indirect calorimetry and immunoblotting to determine whole body glucose and fat oxidation, leg glucose uptake, muscle AMPKalpha2 activity, and the phosphorylation of muscle Akt and AS160/TBC1D4. Glucose oxidation was reduced while fat oxidation increased ( approximately 35%) during postexercise recovery (P <or= 0.05). Glucose uptake increased during exercise and postexercise recovery (P <or= 0.05). Akt phosphorylation was increased at 1 h and AMPKalpha2 activity increased at 2 h postexercise (P <or= 0.05). Phospho(Ser/Thr)-Akt substrate (PAS) phosphorylation (often used as a marker for AS160) was unchanged immediately postexercise and increased at 1 h (P <or= 0.05) and 2 h postexercise (P = 0.07). The PAS antibody is not always specific for AS160/TBC1D4 and can detect proteins at a similar molecular weight. Therefore, we immunoprecipitated AS160/TBC1D4 and then blotted with the PAS antibody, which confirmed that PAS phosphorylation is occurring on AS160/TBC1D4. There was also a positive correlation between PAS phosphorylation and leg glucose uptake during recovery (P < 0.05). We conclude that resistance exercise increases AS160/TBC1D4 phosphorylation in association with an increase in leg glucose uptake during postexercise recovery.
160 kDa的Akt底物(AS160/TBC1D4)与胰岛素及收缩介导的葡萄糖摄取相关。有氧运动期间,人体骨骼肌AS160磷酸化增加,但抗阻运动后不会立即增加。目前尚不清楚抗阻运动恢复过程中AS160磷酸化是否会发生改变。因此,我们推测抗阻运动恢复期间,腿部肌肉AS160/TBC1D4磷酸化及葡萄糖摄取会增加。我们对9名男性受试者在运动前、运动期间及运动后恢复2小时的情况进行了研究。我们采用股动脉插管和肌肉活检,结合间接测热法和免疫印迹法,以确定全身葡萄糖和脂肪氧化、腿部葡萄糖摄取、肌肉AMPKalpha2活性以及肌肉Akt和AS160/TBC1D4的磷酸化情况。运动后恢复期间,葡萄糖氧化减少,而脂肪氧化增加(约35%)(P≤0.05)。运动期间及运动后恢复期间,葡萄糖摄取增加(P≤0.05)。运动后1小时Akt磷酸化增加,运动后2小时AMPKalpha2活性增加(P≤0.05)。磷酸化(丝氨酸/苏氨酸)-Akt底物(PAS)磷酸化(常用作AS160的标志物)在运动后即刻未发生变化,在运动后1小时增加(P≤0.05),在运动后2小时增加(P = 0.07)。PAS抗体并非总是对AS160/TBC1D4具有特异性,且能检测到分子量相似的蛋白质。因此,我们免疫沉淀了AS160/TBC1D4,然后用PAS抗体进行印迹分析,证实PAS磷酸化发生在AS160/TBC1D4上。恢复期间,PAS磷酸化与腿部葡萄糖摄取之间也存在正相关(P < 0.05)。我们得出结论,抗阻运动可增加AS160/TBC1D4磷酸化,并与运动后恢复期间腿部葡萄糖摄取增加相关。