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饥饿对人体骨骼肌中全身碳水化合物分配、产热及解偶联蛋白3表达的影响。

The effects of underfeeding on whole-body carbohydrate partitioning, thermogenesis and uncoupling protein 3 expression in human skeletal muscle.

作者信息

Seevaratnam N, Bennett A J, Webber J, Macdonald I A

机构信息

School of Biomedical Sciences, University of Nottingham Medical School, Nottingham, UK.

出版信息

Diabetes Obes Metab. 2007 Sep;9(5):669-78. doi: 10.1111/j.1463-1326.2006.00646.x.

Abstract

AIM

Underfeeding is known to reduce resting energy expenditure (REE) as an energy-conserving mechanism and may also reduce insulin sensitivity. Uncoupling protein 1 is known to have a significant role in energy expenditure (EE) in small mammals, but the role of UCPs in humans is unclear. UCP3 is primarily expressed in human skeletal muscle, a significant site of whole-body EE in lean individuals and therefore has a potential role in human metabolism. Here, we examine the effects of short-term underfeeding on UCP3 skeletal muscle expression, and on whole-body insulin sensitivity, substrate utilization and thermogenesis.

METHODS

Eleven non-obese men [age 22.8 +/- 1.34 years, body mass index 23.4 +/- 0.71 kg/m(2), mean +/- s.e.m.] were fed for two periods of 6 days, an underfeeding diet (UF) (50% predicted requirements for weight maintenance) and an eucaloric diet (EU), with the same macronutrient composition, in random order. Subjects visited the laboratory on four separate occasions, before and after each dietary period. REE, metabolites and muscle biopsies (vastus lateralis) were taken and the thermogenic response to a hyperinsulinaemic euglycaemic clamp was measured over a 2-h period. UCP3 mRNA levels were measured using Taqman.

RESULTS

After underfeeding for 6 days, REE fell by 0.43 +/- 0.17 kJ/min (p = 0.032), with weight loss of 2.05 +/- 0.34 kg (p < 0.001). Baseline fasting glucose was significantly lower at 4.26 +/- 0.07 mmol/l (p = 0.005), with a corresponding fall in carbohydrate oxidation (0.08 +/- 0.03 g/min; p = 0.04). Fasting free fatty acids (FFA) increased by 0.13 +/- 0.03 mmol/l (p < 0.001), with an increase in beta-hydroxybutyrate concentrations of 0.41 +/- 0.07 mM (p < 0.001) compared with post-EU. There was no significant change in UCP3 mRNA levels pre- and post-UF [10.4 +/- 6.8 arbitrary units (au); p = 0.16] compared with pre- and post-EU (3.2 +/- 7.3 au; p = 0.67). There was no thermogenic response to the clamp after 6 days of underfeeding and a significant reduction in glucose disposal rates (from 46.35 +/- 2.15 to 39.46 +/- 1.12 micromol/min/kg; p = 0.003). Carbohydrate oxidation rates were lower by 0.08 +/- 0.03 g/min (p = 0.011) compared with pre-UF, with no change in glucose storage rates (28.2 +/- 2.4 micromol/min/kg pre-UF; 27.0 +/- 2.3 micromol/min/kg post-UF; p = 0.7). EU resulted in a mildly underfed state with marginal weight loss (0.55 +/- 0.28 kg; p = 0.08), and fasting FFA increased by 0.13 +/- 0.03 mmol/l (p < 0.001) and beta-hydroxybutyrate concentrations by 0.05 +/- 0.02 mM (p = 0.03) compared with pre-EU. There was no change in glucose disposal or storage rates compared with pre-EU.

CONCLUSIONS

Underfeeding for 6 days has no significant effect on UCP3 mRNA expression in skeletal muscle in non-obese men but is associated with changes in carbohydrate fuel partitioning, REE and the thermogenic response to the glucose clamp. Mild underfeeding had no effect on insulin sensitivity, but more severe energy restriction reduced insulin-stimulated glucose oxidation without affecting glucose storage.

摘要

目的

已知营养不足作为一种节能机制会降低静息能量消耗(REE),并且可能还会降低胰岛素敏感性。解偶联蛋白1在小型哺乳动物的能量消耗(EE)中具有重要作用,但解偶联蛋白(UCPs)在人类中的作用尚不清楚。UCP3主要在人类骨骼肌中表达,而骨骼肌是瘦人全身EE的一个重要部位,因此在人类新陈代谢中具有潜在作用。在此,我们研究短期营养不足对UCP3骨骼肌表达、全身胰岛素敏感性、底物利用和产热的影响。

方法

11名非肥胖男性[年龄22.8±1.34岁,体重指数23.4±0.71kg/m²,均值±标准误]被随机安排接受两个为期6天的饮食阶段,即营养不足饮食(UF)(维持体重所需预测热量的50%)和等热量饮食(EU),两种饮食的宏量营养素组成相同。受试者在每个饮食阶段前后各有四次分别前往实验室。测量REE、代谢物并采集肌肉活检样本(股外侧肌),并在2小时内测量对高胰岛素正常血糖钳夹的产热反应。使用Taqman法测量UCP3 mRNA水平。

结果

营养不足6天后,REE下降了0.43±0.17kJ/分钟(p = 0.032),体重减轻了2.05±0.34kg(p < 0.001)。基线空腹血糖显著降低至4.26±0.07mmol/L(p = 0.005),同时碳水化合物氧化相应减少(0.08±0.03g/分钟;p = 0.04)。空腹游离脂肪酸(FFA)增加了0.13±0.03mmol/L(p < 0.001),与EU后相比,β-羟基丁酸浓度增加了0.41±0.07mM(p < 0.001)。与EU前后相比,UF前后UCP3 mRNA水平无显著变化[10.4±6.8任意单位(au);p = 0.16](3.2±7.3au;p = 0.67)。营养不足6天后对钳夹无产热反应,葡萄糖处置率显著降低(从46.35±2.15降至39.46±1.12微摩尔/分钟/千克;p = 0.003)。与UF前相比,碳水化合物氧化率降低了0.08±0.03g/分钟(p = 0.011),葡萄糖储存率无变化(UF前28.2±2.4微摩尔/分钟/千克;UF后27.0±2.3微摩尔/分钟/千克;p = 0.7)。EU导致轻度营养不足状态,体重略有减轻(0.55±0.28kg;p = 0.08),与EU前相比,空腹FFA增加了0.13±0.03mmol/L(p < 0.001),β-羟基丁酸浓度增加了0.05±0.02mM(p = 0.03)。与EU前相比,葡萄糖处置或储存率无变化。

结论

6天的营养不足对非肥胖男性骨骼肌中UCP3 mRNA表达无显著影响,但与碳水化合物燃料分配、REE以及对葡萄糖钳夹的产热反应变化有关。轻度营养不足对胰岛素敏感性无影响,但更严重的能量限制会降低胰岛素刺激的葡萄糖氧化,而不影响葡萄糖储存。

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