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胰岛素对肥胖青少年甘油生成的影响。

Effect of insulin on glycerol production in obese adolescents.

作者信息

Robinson C, Tamborlane W V, Maggs D G, Enoksson S, Sherwin R S, Silver D, Shulman G I, Caprio S

机构信息

Department of Pediatrics, Yale University School of Medicine, New Haven, Connecticut 06520, USA.

出版信息

Am J Physiol. 1998 Apr;274(4):E737-43. doi: 10.1152/ajpendo.1998.274.4.E737.

Abstract

Impaired stimulation of glucose metabolism and reduced suppression of lipolytic activity have both been suggested as important defects related to the insulin resistance of adolescent obesity. To further explore the relationship between these abnormalities, we studied seven obese [body mass index (BMI) 35 +/- 2 kg/m2] and seven lean (BMI 21 +/- 1 kg/m2) adolescents aged 13-15 yr and compared them with nine lean adults (aged 21-27 yr, BMI 23 +/- 1 kg/m2) during a two-step euglycemic-hyperinsulinemic clamp in combination with 1) a constant [2H5]glycerol (1.2 mg.m-2.min-1) infusion to quantify glycerol turnover and 2) indirect calorimetry to estimate glucose and net lipid oxidation rates. In absolute terms, basal glycerol turnover was increased and suppression by insulin was impaired in obese adolescents compared with both groups of lean subjects (P < 0.01). However, when the rates of glycerol turnover were adjusted for differences in body fat mass, the rates were similar in all three groups. Basal plasma free fatty acid (FFA) concentrations were significantly elevated, and the suppression by physiological increments in plasma insulin was impaired in obese adolescents compared with lean adults (P < 0.05). In parallel with the high circulating FFA levels, net lipid oxidation in the basal state and during the clamp was also elevated in the obese group compared with lean adults. Net lipid oxidation was inversely correlated with glucose oxidation (r = -0.50, P < 0.01). In conclusion, these data suggest that lipolysis is increased in obese adolescents (vs. lean adolescents and adults) as a consequence of an enlarged adipose mass rather than altered sensitivity of adipocytes to the suppressing action of insulin.

摘要

葡萄糖代谢刺激受损和脂肪分解活性抑制减弱均被认为是与青少年肥胖胰岛素抵抗相关的重要缺陷。为了进一步探究这些异常之间的关系,我们研究了7名肥胖青少年(体重指数BMI为35±2kg/m²)和7名瘦青少年(BMI为21±1kg/m²),年龄在13 - 15岁,并在两步正常血糖 - 高胰岛素钳夹实验中将他们与9名瘦成年人(年龄21 - 27岁,BMI为23±1kg/m²)进行比较,该实验结合了:1)持续输注[²H₅]甘油(1.2mg·m⁻²·min⁻¹)以量化甘油周转率;2)间接测热法以估计葡萄糖和净脂质氧化率。就绝对值而言,与两组瘦受试者相比,肥胖青少年的基础甘油周转率增加且胰岛素对其的抑制受损(P < 0.01)。然而,当根据体脂量差异调整甘油周转率时,三组的周转率相似。肥胖青少年的基础血浆游离脂肪酸(FFA)浓度显著升高,与瘦成年人相比,血浆胰岛素生理性升高对其的抑制受损(P < 0.05)。与高循环FFA水平平行,肥胖组基础状态和钳夹期间的净脂质氧化也高于瘦成年人。净脂质氧化与葡萄糖氧化呈负相关(r = -0.50,P < 0.01)。总之,这些数据表明,肥胖青少年(与瘦青少年和成年人相比)脂肪分解增加是由于脂肪量增加,而非脂肪细胞对胰岛素抑制作用的敏感性改变。

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