Turku PET Centre, University of Turku, Turku, Finland.
Section on Integrative Physiology and Metabolism, Joslin Diabetes Center, Harvard Medical School, Boston, Massachusetts.
Diabetes Obes Metab. 2017 Oct;19(10):1379-1388. doi: 10.1111/dom.12947. Epub 2017 Jul 6.
To test the hypothesis that high-intensity interval training (HIIT) and moderate-intensity continuous training (MICT) improve brown adipose tissue (BAT) insulin sensitivity.
Healthy middle-aged men (n = 18, age 47 years [95% confidence interval {CI} 49, 43], body mass index 25.3 kg/m [95% CI 24.1-26.3], peak oxygen uptake (VO ) 34.8 mL/kg/min [95% CI 32.1, 37.4] ) were recruited and randomized into six HIIT or MICT sessions within 2 weeks. Insulin-stimulated glucose uptake was measured using 2-[ F]flouro-2-deoxy-D-glucose positron-emission tomography in BAT, skeletal muscle, and abdominal and femoral subcutaneous and visceral white adipose tissue (WAT) depots before and after the training interventions.
Training improved VO (P = .0005), insulin-stimulated glucose uptake into the quadriceps femoris muscle (P = .0009) and femoral subcutaneous WAT (P = .02) but not into BAT, with no difference between the training modes. Using pre-intervention BAT glucose uptake, we next stratified subjects into high BAT (>2.9 µmol/100 g/min; n = 6) or low BAT (<2.9 µmol/100 g/min; n = 12) groups. Interestingly, training decreased insulin-stimulated BAT glucose uptake in the high BAT group (4.0 [2.8, 5.5] vs 2.5 [1.7, 3.6]; training*BAT, P = .02), whereas there was no effect of training in the low BAT group (1.5 [1.2, 1.9] vs 1.6 [1.2, 2.0] µmol/100 g/min). Participants in the high BAT group had lower levels of inflammatory markers compared with those in the low BAT group.
Participants with functionally active BAT have an improved metabolic profile compared with those with low BAT activity. Short-term exercise training decreased insulin-stimulated BAT glucose uptake in participants with active BAT, suggesting that training does not work as a potent stimulus for BAT activation.
验证高强度间歇训练(HIIT)和中等强度持续训练(MICT)是否能提高棕色脂肪组织(BAT)的胰岛素敏感性。
健康的中年男性(n=18,年龄 47 岁[95%置信区间{CI}49,43],体重指数 25.3kg/m[95%CI24.1-26.3],峰值摄氧量(VO )34.8mL/kg/min[95%CI32.1,37.4])在 2 周内被招募并随机分为 6 组进行 HIIT 或 MICT。在训练干预前后,使用 2-[F]氟-2-脱氧-D-葡萄糖正电子发射断层扫描测量 BAT、骨骼肌以及腹部和股部皮下和内脏白色脂肪组织(WAT)中的胰岛素刺激葡萄糖摄取。
训练提高了 VO(P=0.0005)、股四头肌肌肉的胰岛素刺激葡萄糖摄取(P=0.0009)和股部皮下 WAT(P=0.02),但对 BAT 没有影响,两种训练模式之间没有差异。根据 BAT 葡萄糖摄取的干预前水平,我们进一步将受试者分为高 BAT(>2.9µmol/100g/min;n=6)或低 BAT(<2.9µmol/100g/min;n=12)组。有趣的是,训练降低了高 BAT 组的胰岛素刺激 BAT 葡萄糖摄取(4.0[2.8,5.5]vs2.5[1.7,3.6];训练*BAT,P=0.02),而在低 BAT 组中训练没有影响(1.5[1.2,1.9]vs1.6[1.2,2.0]µmol/100g/min)。高 BAT 组的参与者的炎症标志物水平低于低 BAT 组。
与低 BAT 活性的参与者相比,具有功能性活性 BAT 的参与者具有改善的代谢特征。短期运动训练降低了具有活跃 BAT 的参与者的胰岛素刺激 BAT 葡萄糖摄取,表明训练不是 BAT 激活的有效刺激。