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首页> 外文期刊>The Journal of Physiology >Exercise training reduces the insulin-sensitizing effect of a single bout of exercise in human skeletal muscle
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Exercise training reduces the insulin-sensitizing effect of a single bout of exercise in human skeletal muscle

机译:运动培训减少了在人骨骼肌中单个锻炼的胰岛素敏感效果

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摘要

Not only chronic exercise training, but also a single bout of exercise, increases insulin-stimulated glucose uptake in skeletal muscle. However, it is not well described how adaptations to exercise training affect the ability of a single bout of exercise to increase insulin sensitivity. Rodent studies suggest that the insulin-sensitizing effect of a single bout of exercise is AMPK-dependent (presumably via the alpha(2)beta(2)gamma(3) AMPK complex). Whether this is also the case in humans is unknown. Previous studies have shown that exercise training decreases the expression of the alpha(2)beta(2)gamma(3) AMPK complex and diminishes the activation of this complex during exercise. Thus, we hypothesized that exercise training diminishes the ability of a single bout of exercise to enhance muscle insulin sensitivity. We investigated nine healthy male subjects who performed one-legged knee-extensor exercise at the same relative intensity before and after 12 weeks of exercise training. Training increased (V) over dot(O2 peak) and expression of mitochondrial proteins in muscle, whereas the expression of AMPK gamma 3 was decreased. Training also increased whole body and muscle insulin sensitivity. Interestingly, insulin-stimulated glucose uptake in the acutely exercised leg was not enhanced further by training. Thus, the increase in insulin-stimulated glucose uptake following a single bout of one-legged exercise was lower in the trained vs. untrained state. This was associated with reduced signalling via confirmed alpha(2)beta(2)gamma(3) AMPK downstream targets (ACC and TBC1D4). These results suggest that the insulin-sensitizing effect of a single bout of exercise is also AMPK-dependent in human skeletal muscle.
机译:不仅慢性运动训练,而且还增加了一个运动,增加了骨骼肌刺激的葡萄糖摄取。然而,它没有详细描述运动训练的适应如何影响单一锻炼以增加胰岛素敏感性的能力。啮齿动物的研究表明,锻炼的单个回合的胰岛素增敏作用是AMPK依赖性(通过α(2)测试推测(2)的γ(3)AMPK络合物)。这也是人类的情况是未知的。之前的研究表明,运动训练降低了α(2)β(2)γ(3)AMPK复合物的表达,并在运动期间减少了这种复合物的活化。因此,我们假设运动培训减少了单一锻炼以增强肌肉胰岛素敏感性的能力。我们调查了九个健康的男性受试者,在运动培训12周之前和之后,在相同的相对强度下进行单腿膝盖伸展运动。训练越来越多(v)肌肉(o2峰)和肌肉中线粒体蛋白的表达,而AMPKγ3的表达减少。培训也增加了全身和肌肉胰岛素敏感性。有趣的是,通过培训进一步增强了急性锻炼腿中的胰岛素刺激的葡萄糖摄取。因此,在训练的与未经训练的状态下,单个腿锻炼之后的胰岛素刺激的葡萄糖摄取的增加较低。这与通过确认的α(2)β(2)γ(3)AMPK下游靶标(ACC和TBC1D4)的信号传导降低的信号传导相关。这些结果表明,单一锻炼的胰岛素敏化效应也依赖于人骨骼肌。

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