Saloranta C, Franssila-Kallunki A, Ekstrand A, Taskinen M R, Groop L
Third Department of Medicine, Helsinki University Hospital, Finland.
Diabetologia. 1991 Jun;34(6):409-15. doi: 10.1007/BF00403179.
To study the effect of changes in plasma non-esterified fatty acid concentration on suppression of hepatic glucose production by insulin eight Type 2 (non-insulin-dependent) diabetic patients participated in three euglycaemic, hyperinsulinaemic (108pmol.m2-1.min-1) clamp studies combined with indirect calorimetry and infusion of [3-3H]-glucose and [1-14C]palmitate; (1) a control experiment with infusion of NaCl 154 mmol/l, (2) heparin was infused together with insulin, and (3) an antilipolytic agent, Acipimox, was administered at the beginning of the experiment. Six healthy volunteers participated in the control experiment. Plasma non-esterified fatty acid concentrations during the insulin clamp were in diabetic patients: (1) 151 +/- 36 mumol/l, (2) 949 +/- 178 mumol/l, and (3) 65 +/- 9 mumol/l; in healthy control subjects 93 +/- 13 mumol/l. Non-esterified fatty acid transport rate, oxidation and non-oxidative metabolism were significantly higher during the heparin than during the Acipimox experiment (p less than 0.001). Suppression of hepatic glucose production by insulin was impaired in the diabetic compared to control subjects (255 +/- 42 vs 51 +/- 29 mumol/min, p less than 0.01). Infusion of heparin did not affect the suppression of hepatic glucose production by insulin (231 +/- 49 mumol/min), whereas Acipimox significantly enhanced the suppression (21 +/- 53 mumol/min, p less than 0.001 vs 154 mmol/l NaCl experiment). We conclude that insulin-mediated suppression of hepatic glucose production is not affected by increased non-esterified fatty acid availability. In contrast, decreased non-esterified fatty acid availability enhances the suppression of hepatic glucose production by insulin.
为研究血浆非酯化脂肪酸浓度变化对胰岛素抑制肝葡萄糖生成作用的影响,8名2型(非胰岛素依赖型)糖尿病患者参与了三项正常血糖、高胰岛素血症(108pmol·m²⁻¹·min⁻¹)钳夹研究,并结合间接测热法以及[3-³H] -葡萄糖和[1-¹⁴C]棕榈酸酯输注;(1)输注154mmol/l氯化钠的对照实验;(2)肝素与胰岛素一起输注;(3)在实验开始时给予抗脂解剂阿西莫司。6名健康志愿者参与了对照实验。胰岛素钳夹期间糖尿病患者的血浆非酯化脂肪酸浓度分别为:(1)151±36μmol/l,(2)949±178μmol/l,(3)65±9μmol/l;健康对照受试者为93±13μmol/l。肝素实验期间非酯化脂肪酸转运速率、氧化和非氧化代谢显著高于阿西莫司实验(p<0.001)。与对照受试者相比,糖尿病患者中胰岛素对肝葡萄糖生成的抑制受损(255±42 vs 51±29μmol/min,p<0.01)。输注肝素不影响胰岛素对肝葡萄糖生成的抑制(231±49μmol/min),而阿西莫司显著增强了这种抑制作用(21±53μmol/min,与154mmol/l氯化钠实验相比p<0.001)。我们得出结论,胰岛素介导的肝葡萄糖生成抑制不受非酯化脂肪酸可用性增加的影响。相反,非酯化脂肪酸可用性降低会增强胰岛素对肝葡萄糖生成的抑制作用。