Morton Tiffany L, Galior Kornelia, McGrath Cody, Wu Xin, Uzer Gunes, Uzer Guniz Bas, Sen Buer, Xie Zhihui, Tyson David, Rubin Janet, Styner Maya
Department of Medicine, Division of Endocrinology and Metabolism, University of North Carolina at Chapel Hill , Chapel Hill, NC , USA.
Front Endocrinol (Lausanne). 2016 Jun 30;7:80. doi: 10.3389/fendo.2016.00080. eCollection 2016.
Muscle lipid increases with high-fat feeding and diabetes. In trained athletes, increased muscle lipid is not associated with insulin resistance, a phenomenon known as the athlete's paradox. To understand if exercise altered the phenotype of muscle lipid, female C57BL/6 mice fed CTL or high-fat diet (HFD for 6 or 18 weeks) were further divided into sedentary or exercising groups (CTL-E or HFD-E) with voluntary access to running wheels for the last 6 weeks of experiments, running 6 h/night. Diet did not affect running time or distance. HFD mice weighed more than CTL after 18 weeks (p < 0.01). Quadriceps muscle TG was increased in running animals and in sedentary mice fed HFD for 18 weeks (p < 0.05). In exercised animals, markers of fat, Plin1, aP2, FSP27, and Fasn, were increased significantly in HFD groups. Ucp1 and Pgc1a, markers for brown fat, increased with exercise in the setting of high fat feeding. Fndc5, which encodes irisin, and CytC were sensitive to exercise regardless of diet. Plin5 was increased with HFD and unaffected by exercise; the respiratory exchange ratio was 15% lower in the 18-week HFD group compared with CTL (p < 0.001) and 10% lower in 18 weeks HFD-E compared with CTL-E (p < 0.001). Increased Ucp1 and Pgc1a in exercised muscle of running mice suggests that a beige/brown fat phenotype develops, which differs from the fat phenotype that induces insulin resistance in high fat feeding. This suggests that increased muscle lipid may develop a "brown" phenotype in the setting of endurance exercise training, a shift that is further promoted by HFD.
高脂肪饮食和糖尿病会导致肌肉脂质增加。在训练有素的运动员中,肌肉脂质增加与胰岛素抵抗无关,这一现象被称为运动员悖论。为了了解运动是否会改变肌肉脂质的表型,将喂食对照饮食(CTL)或高脂饮食(HFD,持续6周或18周)的雌性C57BL/6小鼠进一步分为久坐组或运动组(CTL-E或HFD-E),在实验的最后6周让它们自由使用跑步轮,每晚跑步6小时。饮食对跑步时间或距离没有影响。18周后,HFD小鼠的体重比CTL小鼠更重(p<0.01)。在跑步的动物以及喂食HFD 18周的久坐小鼠中,股四头肌甘油三酯(TG)增加(p<0.05)。在运动的动物中,HFD组中脂肪标记物Plin1、aP2、FSP27和Fasn显著增加。在高脂喂养情况下,棕色脂肪标记物Ucp1和Pgc1a随运动增加。无论饮食如何,编码鸢尾素的Fndc5和细胞色素C(CytC)对运动敏感。Plin5随HFD增加且不受运动影响;18周HFD组的呼吸交换率比CTL组低15%(p<0.001),18周HFD-E组比CTL-E组低10%(p<0.001)。跑步小鼠运动肌肉中Ucp1和Pgc1a增加表明出现了米色/棕色脂肪表型,这与高脂喂养中诱导胰岛素抵抗的脂肪表型不同。这表明在耐力运动训练情况下,增加的肌肉脂质可能会形成一种“棕色”表型,高脂饮食会进一步促进这种转变。