Storgaard Heidi, Jensen Christine B, Vaag Allan A, Vølund Aage, Madsbad Sten
Department of Endocrinology, Hvidovre Hospital, University of Copenhagen, Denmark.
Metabolism. 2003 Jul;52(7):885-94. doi: 10.1016/s0026-0495(03)00102-1.
We studied the effect of a low-grade short- and long-term 20% Intralipid infusion (0.4 mL(-1) x kg(-1) x h(-1)) on insulin secretion and insulin action in 15 elderly obese men; 7 glucose intolerant first-degree relatives of type 2 diabetic patients (impaired glucose tolerance [IGT] relatives) and 8 healthy controls of similar age and body mass index (BMI). Intravenous glucose tolerance test (IVGTT) and a graded glucose infusion (dose-response test [DORE]) were performed to determine first phase insulin response and to explore the dose response relationship between glucose concentration and insulin secretion rates (ISR). ISR were calculated by deconvolution of plasma C-peptide concentrations. Insulin action was determined by performing a 120-minute hyperinsulinemic euglycemic clamp. All tests were performed 3 times, preceded by 0, 2, or 24 hours Intralipid infusion. Disposition indices (DI) were calculated for the IVGTT. Insulin action was reduced 25% after 2 and 24 hours Intralipid infusion in both groups. In IGT relatives, the beta-cell responsiveness to glucose (measured during DORE) decreased after 2 and 24 hours Intralipid infusion (P=.02), whereas first phase insulin response (measured during IVGTT) decreased after 24 hours Intralipid infusion. Insulin secretion measured during DORE and IVGTT was not affected by Intralipid infusion in controls. DI decreased after 2 and 24 hours Intralipid infusion in the total study population. In conclusion, insulin resistance induced by low-grade short- and long-term Intralipid infusion is not balanced by an adequate compensatory increase in insulin secretion in IGT relatives or in matched controls. IGT relatives appear to be more sensitive to the deleterious effects of low-grade fat infusion on insulin secretion than normal glucose tolerant control subjects.
我们研究了低剂量短期和长期20%脂肪乳输注(0.4 mL⁻¹×kg⁻¹×h⁻¹)对15名老年肥胖男性、7名2型糖尿病患者的糖耐量受损一级亲属(糖耐量受损[IGT]亲属)以及8名年龄和体重指数(BMI)相似的健康对照者胰岛素分泌和胰岛素作用的影响。进行静脉葡萄糖耐量试验(IVGTT)和分级葡萄糖输注(剂量反应试验[DORE])以确定第一相胰岛素反应,并探索葡萄糖浓度与胰岛素分泌率(ISR)之间的剂量反应关系。通过对血浆C肽浓度进行反卷积计算ISR。通过进行120分钟的高胰岛素正常血糖钳夹来确定胰岛素作用。所有测试均在脂肪乳输注0、2或24小时后进行3次。计算IVGTT的处置指数(DI)。两组在脂肪乳输注2小时和24小时后胰岛素作用均降低25%。在IGT亲属中,脂肪乳输注2小时和24小时后,β细胞对葡萄糖的反应性(在DORE期间测量)降低(P = 0.02),而脂肪乳输注24小时后第一相胰岛素反应(在IVGTT期间测量)降低。在对照者中,DORE和IVGTT期间测量的胰岛素分泌不受脂肪乳输注的影响。在整个研究人群中,脂肪乳输注2小时和24小时后DI降低。总之,低剂量短期和长期脂肪乳输注诱导的胰岛素抵抗在IGT亲属或匹配的对照者中未被胰岛素分泌的充分代偿性增加所平衡。与糖耐量正常的对照受试者相比,IGT亲属似乎对低剂量脂肪输注对胰岛素分泌的有害影响更敏感。