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首页> 外文期刊>American Journal of Physiology >Muscle interleukin-6 and fasting-induced PDH regulation in mouse skeletal muscle
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Muscle interleukin-6 and fasting-induced PDH regulation in mouse skeletal muscle

机译:肌肉白细胞介素-6和小鼠骨骼肌中的禁食诱导的PDH调节

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Gudiksen A, Bertholdt L, Vingborg MB, Hansen HW, Ring-holm S, Pilegaard H. Muscle interleukin-6 and fasting-induced PDH regulation in mouse skeletal muscle. Am J Physiol Endocrinol Metab 312: E204-E214, 2017. First published December 27, 2016; doi: 10.1152/ajpendo.00291.2016.—Fasting prompts a metabolic shift in substrate utilization from carbohydrate to predominant fat oxidation in skeletal muscle, and pyruvate dehydrogenase (PDH) is seen as a controlling link between the competitive oxidation of carbohydrate and fat during metabolic challenges like fasting. Interleukin (IL)-6 has been proposed to be released from muscle with concomitant effects on both glucose and fat utilization. The aim was to test the hypothesis that muscle IL-6 has a regulatory impact on fasting-induced suppression of skeletal muscle PDH. Skeletal muscle-specific IL-6 knockout (IL-6 MKO) mice and floxed littermate controls (control) were either fed or fasted for 6 or 18 h. Lack of muscle IL-6 elevated the respiratory exchange ratio in the fed and early fasting state, but not with prolonged fasting. Activity of PDH in the active form (PDHa) was higher in fed and fasted IL-6 MKO than in control mice at 18 h, but not at 6 h, whereas lack of muscle IL-6 did not prevent down-regulation of PDHa activity in skeletal muscle or changes in plasma and muscle substrate levels in response to 18 h of fasting. Phosphor-ylation of three of four sites on PDH-E1alpha increased with 18 h of fasting, but was lower in IL-6 MKO mice than in control. In addition, both PDK4 mRNA and protein increased with 6 and 18 h of fasting in both genotypes, but PDK4 protein was lower in IL-6 MKO than in control. In conclusion, skeletal muscle IL-6 seems to regulate whole body substrate utilization in the fed, but not fasted, state and influence skeletal muscle PDHa activity in a circadian manner. However, skeletal muscle IL-6 is not required for maintaining metabolic flexibility in response to fasting.
机译:Gudiksen A,Bertholdt L,Vingborg MB,Hansen HW,Ring-Holm S,Pipgaard H.肌肉白细胞介素-6和小鼠骨骼肌中的禁食诱导的PDH调节。 AM j Physocrinol Metab 312:E204-E214,2017。2016年12月27日第一次出版; DOI:10.1152 / ajpendo.00291.2016. - 禁食提示从碳水化合物中的衬底利用代谢移位,以骨骼肌中的主要脂肪氧化,并且丙酮酸脱氢酶(PDH)被视为代谢挑战期间碳水化合物和脂肪竞争性氧化之间的控制联系喜欢禁食。已经提出了白细胞介素(IL)-6,以从肌肉释放,伴随着葡萄糖和脂肪利用的影响。目的是测试肌肉IL-6对腹部肌肉PDH的禁食抑制具有调节性影响的假设。骨骼肌特异性IL-6敲除(IL-6 MKO)小鼠和氟化的偶体对照(对照)喂养或禁食6或18小时。缺乏肌肉IL-6在美联储和早期禁食状态下升高了呼吸交换比,但没有延长禁食。活性形式(PDHA)中PDH的活性在喂养和禁食IL-6 MKO中比在18小时的对小鼠中较高,但不是6小时,而缺乏肌肉IL-6并未阻止抑制PDHA活性的调节在骨骼肌或血浆和肌肉基底水平的变化中,响应于18小时的禁食。 PDH-E1Alpha中三种位点中的三个位点的磷酸化合物随着禁食的18小时而增加,但IL-6 MKO小鼠中的较低量低于对照。此外,PDK4 mRNA和蛋白质在两种基因型中禁食时增加了6和18小时,但IL-6 MKO中的PDK4蛋白比对照效果低。总之,骨骼肌IL-6似乎调节了喂养的全身基质利用,但不禁食,状态,并以昼夜方式影响骨骼肌PDHA活性。然而,不需要骨骼肌IL-6保持响应禁食的代谢柔性。

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