Davis S N, Butler P C, Brown M, Beer S, Sobey W, Hanning I, Home P D, Hales C N, Alberti K G
Department of Medicine, Medical School, Newcastle upon Tyne, UK.
Metabolism. 1991 Sep;40(9):953-61. doi: 10.1016/0026-0495(91)90072-5.
We compared the effects of human proinsulin and human insulin on glucose disposal, suppression of hepatic glucose production (HGP), and intermediary carbohydrate and lipid metabolism. Six young, lean, subjects underwent eight separate euglycemic clamps with low-dose intravenous (IV) infusions of insulin and proinsulin (four each). The insulin infusions gave steady-state levels of 0.08 +/- 0.004 (I1), 0.12 +/- 0.003 (I2), 0.18 +/- 0.07 (I3), and 0.25 +/- 0.06 nmol/L (I4). The proinsulin infusions were chosen to give steady-state levels approximately 20-fold higher on a molar basis than insulin, based on previous findings that proinsulin has only 5% to 10% the biological potency of insulin. Steady-state proinsulin levels were 1.2 +/- 0.04 (P1), 2.8 +/- 0.07 (P2), 4.5 +/- 0.3 (P3), and 6.9 +/- 0.3 nmol/L (P4). HGP was suppressed equally by proinsulin and insulin at the four dose levels. Percentage elevation of glucose disposal was significantly increased during each of the insulin infusions compared with proinsulin: I1 107% +/- 4%, P1 87% +/- 4% (P = .03); I2 143% +/- 7%, P2 125% +/- 12% (P = .01); I3 238% +/- 38%, P3 173% +/- 22% (P = .03); I4 283% +/- 17%, P4 178% +/- 11% (P = .002). Dose-response curve analysis demonstrated that proinsulin stimulated glucose disposal approximately 3.3% compared with insulin. The effectiveness of proinsulin in suppressing HGP was approximately 5% compared with insulin. Plasma nonesterified fatty acids, blood glycerol, and 3-hydroxybutyrate were suppressed by similar amounts during each of the four insulin and proinsulin doses.(ABSTRACT TRUNCATED AT 250 WORDS)
我们比较了人胰岛素原和人胰岛素对葡萄糖处置、肝脏葡萄糖生成(HGP)抑制以及碳水化合物和脂质中间代谢的影响。六名年轻、体型偏瘦的受试者接受了八次单独的正常血糖钳夹试验,通过静脉(IV)低剂量输注胰岛素和胰岛素原(各四次)。胰岛素输注产生的稳态水平分别为0.08±0.004(I1)、0.12±0.003(I2)、0.18±0.07(I3)和0.25±0.06 nmol/L(I4)。根据之前胰岛素原生物活性仅为胰岛素的5%至10%这一发现,选择胰岛素原输注以使稳态水平在摩尔基础上比胰岛素高约20倍。稳态胰岛素原水平分别为1.2±0.04(P1)、2.8±0.07(P2)、4.5±0.3(P3)和6.9±0.3 nmol/L(P4)。在四个剂量水平下,胰岛素原和胰岛素对HGP的抑制作用相同。与胰岛素原相比,在每次胰岛素输注期间,葡萄糖处置的百分比升高显著增加:I1为107%±4%,P1为87%±4%(P = 0.03);I2为143%±7%,P2为125%±12%(P = 0.01);I3为238%±38%,P3为173%±22%(P = 0.03);I4为283%±17%,P4为178%±11%(P = 0.002)。剂量反应曲线分析表明,与胰岛素相比,胰岛素原刺激葡萄糖处置的程度约为3.3%。与胰岛素相比,胰岛素原抑制HGP的效力约为5%。在四次胰岛素和胰岛素原剂量输注的每一次过程中,血浆非酯化脂肪酸、血甘油和3-羟基丁酸的水平被抑制的程度相似。(摘要截选至250词)