首页> 外文期刊>Metabolism: Clinical and Experimental >Activation of atypical protein kinase Czeta toward TC10 is regulated by high-fat diet and aerobic exercise in skeletal muscle.
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Activation of atypical protein kinase Czeta toward TC10 is regulated by high-fat diet and aerobic exercise in skeletal muscle.

机译:高脂饮食和骨骼肌有氧运动可调节非典型蛋白激酶Czeta向TC10的活化。

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We determined whether sustained aerobic exercise reverses high-fat diet-induced impairments in the c-Cbl associated protein (CAP)/Casitas b-lineage lymphoma (c-Cbl) signaling cascade in rodent skeletal muscle. Sprague-Dawley rats were placed into either control (n = 16) or high-fat-fed (n = 32) diet groups for 4 weeks. During a subsequent 4-week experimental period, 16 high-fat-fed rats remained sedentary, 16 high-fat-fed rats completed 4 weeks of exercise training, and control animals were sedentary and remained on the control diet. After the intervention period, animals were subjected to hind limb perfusions in the presence (n = 8 per group) or absence (n = 8 per group) of insulin. In the plasma membrane fractions, neither high-fat feeding nor exercise training altered adaptor protein with PH and SH2 domains, (APS), c-Cbl, or TC10 protein concentrations. In contrast, CAP protein concentration and insulin-stimulated plasma membrane c-Cbl tyrosine phosphorylation were reduced by high-fat feeding; but exercise training reversed these impairments. Of note was that insulin-stimulated atypical protein kinase Czeta kinase activity toward TC10 was reduced by high-fat feeding but normalized by exercise training. We conclude that sustained (4 weeks) exercise training can reverse high-fat diet-induced impairments on the CAP/c-Cbl pathway in high-fat-fed rodent skeletal muscle. We also provide the first evidence that the CAP/c-Cbl insulin signaling cascade in skeletal muscle may directly interact with components of the classic (phosphoinositide 3-kinase dependent) insulin signaling cascade.
机译:我们确定了持续的有氧运动是否能逆转高脂饮食诱导的啮齿动物骨骼肌c-Cbl相关蛋白(CAP)/ Casitas b谱系淋巴瘤(c-Cbl)信号传导障碍。将Sprague-Dawley大鼠分为对照组(n = 16)或高脂饮食(n = 32)饮食组4周。在随后的4周实验期内,有16只高脂饮食大鼠久坐不动,有16只高脂饮食大鼠完成了4周的运动训练,而对照动物则久坐不动并保持对照饮食。干预期过后,在存在胰岛素(每组8只)或不存在胰岛素(每组8只)的情况下对动物进行后肢灌注。在质膜级分中,高脂喂养和运动训练均未改变具有PH和SH2结构域(APS),c-Cbl或TC10蛋白浓度的衔接蛋白。相反,高脂喂养降低了CAP蛋白浓度和胰岛素刺激的质膜c-Cbl酪氨酸磷酸化。但是运动训练可以扭转这些障碍。值得注意的是,高脂喂养降低了胰岛素刺激的非典型蛋白激酶Czeta激酶对TC10的活性,但通过运动训练使其恢复正常。我们得出结论,持续(4周)的运动训练可以逆转高脂饮食啮齿动物骨骼肌中CAP / c-Cbl途径引起的高脂饮食诱导的损伤。我们还提供了第一个证据,即骨骼肌中CAP / c-Cbl胰岛素信号传导级联可能直接与经典(磷酸肌醇3激酶依赖性)胰岛素信号传导级联的成分相互作用。

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