Ferraro R T, Eckel R H, Larson D E, Fontvieille A M, Rising R, Jensen D R, Ravussin E
Clinical Diabetes and Nutrition Section, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Phoenix, Arizona 85016.
J Clin Invest. 1993 Jul;92(1):441-5. doi: 10.1172/JCI116586.
A low ratio of whole-body 24-h fat/carbohydrate (CHO) oxidation has been shown to be a predictor of subsequent body weight gain. We tested the hypothesis that the variability of this ratio may be related to differences in skeletal muscle metabolism. Since lipoprotein lipase (LPL) plays a pivotal role in partitioning lipoprotein-borne triglycerides to adipose (storage) and skeletal muscle (mostly oxidation), we postulated that a low ratio of fat/CHO oxidation was associated with a low skeletal muscle LPL (SMLPL) activity. As an index of substrate oxidation, 24-h RQ was measured under sedentary and eucaloric conditions in 16 healthy nondiabetic Pima males. During a 6-h euglycemic, hyperinsulinemic clamp, muscle biopsies were obtained at baseline, 3, and 6 h. Heparin-elutable SMLPL activity was 2.92 +/- 0.56 nmol free fatty acids/g.min (mean +/- SD) at baseline, was unchanged (2.91 +/- 0.51) at the third hour, and increased significantly (P < 0.05) to 3.13 +/- 0.57 at the sixth hour of the clamp. The mean (of baseline and 3-h) SMLPL activity correlated inversely with 24-h RQ (r = 0.57, P < 0.03) but not with body size, body composition, or insulin-mediated glucose uptake. Since SMLPL activity is related to the ratio of whole body fat/CHO oxidation rate, a decreased muscle LPL activity may, therefore, predispose to obesity.
全身24小时脂肪/碳水化合物(CHO)氧化率较低已被证明是后续体重增加的一个预测指标。我们检验了这样一个假设,即该比率的变异性可能与骨骼肌代谢差异有关。由于脂蛋白脂肪酶(LPL)在将脂蛋白携带的甘油三酯分配到脂肪(储存)和骨骼肌(主要是氧化)中起关键作用,我们推测脂肪/CHO氧化率较低与骨骼肌LPL(SMLPL)活性较低有关。作为底物氧化的指标,在16名健康非糖尿病皮马男性久坐和热量平衡的条件下测量了24小时呼吸商(RQ)。在6小时的正常血糖、高胰岛素钳夹期间,在基线、3小时和6小时获取肌肉活检样本。肝素可洗脱的SMLPL活性在基线时为2.92±0.56 nmol游离脂肪酸/g·分钟(平均值±标准差),在第3小时未改变(2.91±0.51),在钳夹第6小时显著增加(P<0.05)至3.13±0.57。(基线和3小时的)平均SMLPL活性与24小时RQ呈负相关(r = 0.57,P<0.03),但与体型大小(身体尺寸)、身体成分或胰岛素介导的葡萄糖摄取无关。由于SMLPL活性与全身脂肪/CHO氧化率相关,因此,肌肉LPL活性降低可能易导致肥胖。