Colberg S R, Simoneau J A, Thaete F L, Kelley D E
Department of Veterans Affairs Medical Center, University of Pittsburgh School of Medicine, Pennsylvania 15261, USA.
J Clin Invest. 1995 Apr;95(4):1846-53. doi: 10.1172/JCI117864.
Visceral obesity is strongly associated with insulin resistance. One potential cause is increased availability of FFA. Alternatively, it has been proposed that there is impaired oxidation of lipid in individuals at risk for obesity. The extent to which either concept involves skeletal muscle is uncertain. To examine these opposing hypotheses, 17 healthy lean and obese premenopausal women, among whom cross-sectional area of visceral fat ranged from 18 to 180 cm2, participated in leg balance studies for measurement of FFA and glucose utilization during basal and insulin-stimulated conditions. A metabolic profile of skeletal muscle, based on enzyme activity, was determined in vastus lateralis muscle obtained by percutaneous biopsy. Visceral fat content was negatively correlated with insulin sensitivity (rates of leg glucose uptake and storage), but insulin resistance was not caused by glucose-FFA competition. During hyperinsulinemia, neither leg FFA uptake nor oxidation was increased in women with visceral obesity. During fasting conditions, however, rates of FFA uptake across the leg were negatively correlated with visceral adiposity as were activities of muscle carnitine palmitoyl transferase and citrate synthase. In summary, visceral adiposity is clearly associated with skeletal muscle insulin resistance but this is not due to glucose-FFA substrate competition. Instead, women with visceral obesity have reduced postabsorptive FFA utilization by muscle.
内脏性肥胖与胰岛素抵抗密切相关。一个潜在原因是游离脂肪酸(FFA)的可利用性增加。另外,有人提出肥胖风险个体存在脂质氧化受损的情况。这两种观点在多大程度上涉及骨骼肌尚不确定。为了检验这些相反的假设,17名健康的瘦型和肥胖型绝经前女性参与了腿部平衡研究,这些女性的内脏脂肪横截面积在18至180平方厘米之间,研究测量了基础状态和胰岛素刺激状态下的FFA和葡萄糖利用情况。通过经皮活检获取股外侧肌,基于酶活性确定骨骼肌的代谢特征。内脏脂肪含量与胰岛素敏感性(腿部葡萄糖摄取和储存率)呈负相关,但胰岛素抵抗并非由葡萄糖-FFA竞争引起。在内脏性肥胖女性中,高胰岛素血症期间腿部FFA摄取和氧化均未增加。然而,在禁食状态下,腿部FFA摄取率与内脏脂肪量呈负相关,肌肉肉碱棕榈酰转移酶和柠檬酸合酶的活性也与内脏脂肪量呈负相关。总之,内脏性肥胖显然与骨骼肌胰岛素抵抗有关,但这并非由于葡萄糖-FFA底物竞争。相反,内脏性肥胖女性肌肉的餐后FFA利用率降低。