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AMP-activated protein kinase plays an important evolutionary conserved role in the regulation of glucose metabolism in fish skeletal muscle cells

机译:AMP激活的蛋白激酶在鱼骨骼肌细胞葡萄糖代谢的调节中起重要的进化保守作用

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摘要

AMPK, a master metabolic switch, mediates the observed increase of glucose uptake in locomotory muscle of mammals during exercise. AMPK is activated by changes in the intracellular AMP:ATP ratio when ATP consumption is stimulated by contractile activity but also by AICAR and metformin, compounds that increase glucose transport in mammalian muscle cells. However, the possible role of AMPK in the regulation of glucose metabolism in skeletal muscle has not been investigated in other vertebrates, including fish. In this study, we investigated the effects of AMPK activators on glucose uptake, AMPK activity, cell surface levels of trout GLUT4 and expression of GLUT1 and GLUT4 as well as the expression of enzymes regulating glucose disposal and PGC1α in trout myotubes derived from a primary muscle cell culture. We show that AICAR and metformin significantly stimulated glucose uptake (1.6 and 1.3 fold, respectively) and that Compound C completely abrogated the stimulatory effects of the AMPK activators on glucose uptake. The combination of insulin and AMPK activators did not result in additive nor synergistic effects on glucose uptake. Moreover, exposure of trout myotubes to AICAR and metformin resulted in an increase in AMPK activity (3.8 and 3 fold, respectively). We also provide evidence suggesting that stimulation of glucose uptake by AMPK activators in trout myotubes may take place, at least in part, by increasing the cell surface and mRNA levels of trout GLUT4. Finally, AICAR increased the mRNA levels of genes involved in glucose disposal (hexokinase, 6-phosphofructokinase, pyruvate kinase and citrate synthase) and mitochondrial biogenesis (PGC-1α) and did not affect glycogen content or glycogen synthase mRNA levels in trout myotubes. Therefore, we provide evidence, for the first time in non-mammalian vertebrates, suggesting a potentially important role of AMPK in stimulating glucose uptake and utilization in the skeletal muscle of fish.
机译:AMPK是一种主要的新陈代谢转换,可调节运动过程中哺乳动物运动肌中葡萄糖摄取的增加。当收缩活动刺激ATP消耗时,AMPK会被细胞内AMP:ATP比值的变化激活,而AICAR和二甲双胍会刺激哺乳动物肌肉细胞中葡萄糖的转运,从而刺激ATP的消耗。但是,尚未在其他脊椎动物(包括鱼类)中研究过AMPK在调节骨骼肌葡萄糖代谢中的可能作用。在这项研究中,我们调查了AMPK激活剂对鳟鱼肌管中葡萄糖摄取,AMPK活性,鳟鱼GLUT4的细胞表面水平以及GLUT1和GLUT4的表达以及调节葡萄糖处理和PGC1α的酶的表达的影响。细胞培养。我们显示AICAR和二甲双胍显着刺激了葡萄糖摄取(分别为1.6和1.3倍),并且化合物C完全废除了AMPK激活剂对葡萄糖摄取的刺激作用。胰岛素和AMPK激活剂的组合不会对葡萄糖的摄取产生累加或协同作用。此外,鳟鱼肌管暴露于AICAR和二甲双胍导致AMPK活性增加(分别为3.8和3倍)。我们还提供证据表明,鳟鱼肌管中的AMPK激活剂刺激葡萄糖摄取可能至少部分地通过增加鳟鱼GLUT4的细胞表面和mRNA水平来实现。最后,AICAR增加了参与葡萄糖处理的基因(己糖激酶,6-磷酸果糖激酶,丙酮酸激酶和柠檬酸合酶)和线粒体生物发生(PGC-1α)的mRNA水平,并且不影响鳟鱼肌管中的糖原含量或糖原合酶mRNA水平。因此,我们首次在非哺乳动物脊椎动物中提供了证据,表明AMPK在刺激鱼类骨骼肌中葡萄糖的摄取和利用方面具有潜在的重要作用。

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