Groop L C, Bonadonna R C, Simonson D C, Petrides A S, Shank M, DeFronzo R A
Fourth Department of Medicine, Helsinki University Hospital, Finland.
Am J Physiol. 1992 Jul;263(1 Pt 1):E79-84. doi: 10.1152/ajpendo.1992.263.1.E79.
The dose-response relationship between the plasma insulin concentration and oxidative and nonoxidative pathways of free fatty acid (FFA) metabolism was examined in 11 obese and 7 lean subjects using a stepwise insulin clamp technique in combination with indirect calorimetry and infusion of [1-14C]palmitate. The fasting plasma FFA concentration was elevated in obese subjects (793 +/- 43 vs. 642 +/- 39 mumol/l; P less than 0.01) and was associated with an increased basal rate of plasma FFA turnover, FFA oxidation, and nonoxidative FFA disposal, i.e., reesterification (all P less than 0.01). Suppression of plasma FFA turnover by physiological increments in plasma insulin was impaired in obese compared with lean subjects. However, plasma FFA turnover expressed per kilogram fat mass was normally suppressed by insulin in obese subjects. Although insulin suppressed plasma FFA oxidation to the same extent in lean and obese subjects, inhibition of total lipid oxidation by insulin was impaired in the obese group. Obese subjects had an enhanced basal rate of nonoxidative FFA disposal, which was suppressed less by physiological increments in plasma insulin compared with lean controls. Therefore, we conclude that 1) lipolysis in uncomplicated obesity is normally sensitive to insulin; the enhanced FFA flux is simply a consequence of the increased fat mass. 2) Nonoxidative FFA disposal expressed per lean body mass is enhanced in obese subjects and correlates with the increase in plasma FFA concentration and fat mass. 3) Enhanced oxidation of intracellular lipids contributes to the enhanced rate of total lipid oxidation in obese subjects.
采用逐步胰岛素钳夹技术,结合间接测热法和[1-14C]棕榈酸输注,对11名肥胖受试者和7名瘦受试者血浆胰岛素浓度与游离脂肪酸(FFA)代谢的氧化和非氧化途径之间的剂量反应关系进行了研究。肥胖受试者空腹血浆FFA浓度升高(793±43对642±39μmol/l;P<0.01),且与血浆FFA周转率、FFA氧化和非氧化FFA处置(即再酯化)的基础速率增加相关(所有P<0.01)。与瘦受试者相比,肥胖受试者中血浆胰岛素生理性增加对血浆FFA周转率的抑制作用受损。然而,肥胖受试者中按每千克脂肪量计算的血浆FFA周转率通常会被胰岛素抑制。尽管胰岛素在瘦受试者和肥胖受试者中对血浆FFA氧化的抑制程度相同,但肥胖组中胰岛素对总脂质氧化的抑制作用受损。肥胖受试者非氧化FFA处置的基础速率增强,与瘦对照组相比,血浆胰岛素生理性增加对其抑制作用较小。因此,我们得出结论:1)单纯性肥胖中的脂肪分解通常对胰岛素敏感;FFA通量增加仅仅是脂肪量增加的结果。2)肥胖受试者中按瘦体重计算的非氧化FFA处置增强,且与血浆FFA浓度和脂肪量的增加相关。3)细胞内脂质氧化增强导致肥胖受试者总脂质氧化速率增加。