Paz-Filho Gilberto, Esposito Karin, Hurwitz Barry, Sharma Anil, Dong Chuanhui, Andreev Victor, Delibasi Tuncay, Erol Halil, Ayala Alejandro, Wong Ma-Li, Licinio Julio
Dept. of Psychiatry & Behavioral Sciences, Univ. of Miami Miller School of Medicine, Miami, FL 33136, USA.
Am J Physiol Endocrinol Metab. 2008 Dec;295(6):E1401-8. doi: 10.1152/ajpendo.90450.2008. Epub 2008 Oct 14.
Leptin replacement rescues the phenotype of morbid obesity and hypogonadism in leptin-deficient adults. However, leptin's effects on insulin resistance are not well understood. Our objective was to evaluate the effects of leptin on insulin resistance. Three leptin-deficient adults (male, 32 yr old, BMI 23.5 kg/m(2); female, 42 yr old, BMI 25.1 kg/m(2); female, 46 yr old, BMI 31.7 kg/m(2)) with a missense mutation of the leptin gene were evaluated during treatment with recombinant methionyl human leptin (r-metHuLeptin). Insulin resistance was determined by euglycemic hyperinsulinemic clamps and by oral glucose tolerance tests (OGTTs), whereas patients were on r-metHuLeptin and after treatment was interrupted for 2-4 wk in the 4th, 5th, and 6th years of treatment. At baseline, all patients had normal insulin levels, C-peptide, and homeostatic model assessment of insulin resistance index, except for one female diagnosed with type 2 diabetes. The glucose infusion rate was significantly lower with r-metHuLeptin (12.03 +/- 3.27 vs. 8.16 +/- 2.77 mg.kg(-1).min(-1), P = 0.0016) but did not differ in the 4th, 5th, and 6th years of treatment when all results were analyzed by a mixed model [F(1,4) = 0.57 and P = 0.5951]. The female patient with type 2 diabetes became euglycemic after treatment with r-metHuLeptin and subsequent weight loss. The OGTT suggested that two patients showed decreased insulin resistance while off treatment. During an off-leptin OGTT, one of the patients developed a moderate hypoglycemic reaction attributed to increased posthepatic insulin delivery and sensitivity. We conclude that, in leptin-deficient adults, the interruption of r-metHuLeptin decreases insulin resistance in the context of rapid weight gain. Our results suggest that hyperleptinemia may contribute to mediate the increased insulin resistance of obesity.
瘦素替代疗法可改善瘦素缺乏成年人的病态肥胖和性腺功能减退表型。然而,瘦素对胰岛素抵抗的影响尚未完全明确。我们的目的是评估瘦素对胰岛素抵抗的影响。对3名携带瘦素基因错义突变的瘦素缺乏成年人(男性,32岁,体重指数23.5kg/m²;女性,42岁,体重指数25.1kg/m²;女性,46岁,体重指数31.7kg/m²)在接受重组甲硫氨酰人瘦素(r-metHuLeptin)治疗期间进行了评估。通过正常血糖高胰岛素钳夹试验和口服葡萄糖耐量试验(OGTT)测定胰岛素抵抗,测定时间为患者接受r-metHuLeptin治疗期间以及治疗第4、5和6年中断治疗2 - 4周后。基线时,除1名被诊断为2型糖尿病的女性外,所有患者的胰岛素水平、C肽及胰岛素抵抗指数的稳态模型评估均正常。使用r-metHuLeptin时葡萄糖输注率显著降低(12.03±3.27 vs. 8.16±2.77mg·kg⁻¹·min⁻¹,P = 0.0016),但在治疗第4、5和6年,当所有结果通过混合模型分析时,葡萄糖输注率无差异[F(1,4)=0.57,P = 0.5951]。该名2型糖尿病女性患者在接受r-metHuLeptin治疗及随后体重减轻后血糖恢复正常。OGTT结果显示,2名患者在停药期间胰岛素抵抗降低。在停用瘦素的OGTT期间,1名患者出现中度低血糖反应,归因于肝后胰岛素输送增加和敏感性提高。我们得出结论,在瘦素缺乏的成年人中,中断r-metHuLeptin会在体重快速增加的情况下降低胰岛素抵抗。我们的结果表明,高瘦素血症可能有助于介导肥胖时胰岛素抵抗的增加。