VA Research Service, VA Maryland Health Care System, Baltimore, MD, 21201, USA.
Department of Medicine, Division of Gerontology and Geriatric Medicine at the University of Maryland School of Medicine, Baltimore, MD, 21201, USA.
Int J Obes (Lond). 2019 Feb;43(2):276-284. doi: 10.1038/s41366-018-0068-3. Epub 2018 Jun 15.
Obesity and insulin resistance are characterized by metabolic inflexibility, a condition described as an inability to switch from fat oxidation during fasting to carbohydrate oxidation during hyperinsulinemia. The purpose of this study was to examine predictors of metabolic flexibility in 103 obese (37-59% fat), sedentary (VOmax: 19.4 ± 0.5 ml/kg/min), postmenopausal (45-76 years) women, and changes in metabolic flexibility with exercise and weight loss interventions.
Insulin sensitivity (M) and metabolic flexibility via an 80 mU/m/min hyperinsulinemic-euglycemic clamp, VOmax, and body composition were measured. Metabolic flexibility was measured after 6-months aerobic training + weight loss (AEX + WL: n = 43) or weight loss (WL: n = 31). Basal and insulin-stimulated vastus lateralis skeletal muscle samples were available from a subset of these women (n = 45).
Metabolic flexibility correlated inversely with glucose min of OGTT, fasting insulin, and the percent change (insulin-basal) in lipoprotein lipase (LPL) activity and positively with M, but not with VOmax, total body fat, visceral fat, or subcutaneous abdominal fat. Skeletal muscle acyl-CoA synthase and citrate synthase activities decreased during hyperinsulinemia. Metabolic flexibility increased after AEX + WL but not WL, and the percent change in metabolic flexibility was inversely related to the percent change in insulin's effect on LPL activity.
Metabolic flexibility is related to insulin sensitivity and insulin's action on LPL. Furthermore, metabolic flexibility and insulin suppression of skeletal muscle LPL activity increase with AEX + WL in overweight and obese, sedentary older women.
肥胖和胰岛素抵抗的特点是代谢灵活性差,这种情况描述为无法从空腹时的脂肪氧化切换到高胰岛素血症时的碳水化合物氧化。本研究的目的是检查 103 名肥胖(37-59%脂肪)、久坐(VOmax:19.4±0.5ml/kg/min)、绝经后(45-76 岁)女性代谢灵活性的预测因素,以及运动和减肥干预对代谢灵活性的影响。
测量胰岛素敏感性(M)和通过 80mU/m/min 高胰岛素-正常血糖钳夹测量的代谢灵活性、VOmax 和身体成分。在 6 个月有氧运动+减肥(AEX+WL:n=43)或减肥(WL:n=31)后测量代谢灵活性。这些女性中的一部分(n=45)还提供了基础和胰岛素刺激的股外侧肌骨骼肌样本。
代谢灵活性与 OGTT 葡萄糖最小量、空腹胰岛素以及脂蛋白脂肪酶(LPL)活性的胰岛素-基础变化百分比呈负相关,与 M 呈正相关,但与 VOmax、总体脂、内脏脂肪或皮下腹部脂肪无关。在高胰岛素血症期间,骨骼肌酰基辅酶 A 合酶和柠檬酸合酶活性降低。AEX+WL 后代谢灵活性增加,但 WL 后不增加,代谢灵活性的变化百分比与胰岛素对 LPL 活性的影响百分比呈负相关。
代谢灵活性与胰岛素敏感性和胰岛素对 LPL 的作用有关。此外,在超重和肥胖、久坐的老年女性中,AEX+WL 可增加代谢灵活性和胰岛素抑制骨骼肌 LPL 活性。