Jackson R A, Hamling J B, Blix P M, Sim B M, Hawa M I, Jaspan J B, Belin J, Nabarro J D
J Clin Endocrinol Metab. 1986 Sep;63(3):594-604. doi: 10.1210/jcem-63-3-594.
We studied the influence of hyperglycemia on glucose homeostasis in man by determining the effect of graded hyperglycemia on peripheral glucose uptake and systemic metabolism in the presence of basal and increased serum insulin concentrations in 10 normal men. This was achieved by the simultaneous application of forearm and clamp techniques (euglycemic and hyperglycemic) during the combined iv infusion of somatostatin, glucagon, and insulin. While mean (+/- SE) basal serum insulin levels (14 +/- 2 microU/ml) were maintained, the elevation of fasting arterial glucose concentrations (90 +/- 1 mg/dl) to 146 +/- 1 and 202 +/- 1 mg/dl (each for 120 min) increased forearm glucose uptake (FGU) only modestly from 0.06 +/- 0.01 to 0.15 +/- 0.02 and then to 0.24 +/- 0.03 mg/100 ml forearm X min, respectively. During physiological hyperinsulinemia (47 +/- 3 microU/ml), the influence of similar graded hyperglycemia on FGU was considerably enhanced. At plasma glucose concentrations of 90 +/- 1, 139 +/- 1, and 206 +/- 1 mg/dl, FGU rose to 0.33 +/- 0.05, 0.59 +/- 0.07, and 0.83 +/- 0.12 mg/100 ml forearm X min, respectively. The glucose infusion rate required to maintain the glucose clamp with basal insulin levels was 1.08 +/- 0.20 and 2.67 +/- 0.39 mg/kg X min at glucose concentrations of 146 +/- 1 and 202 +/- 1 mg/dl, respectively. During physiological hyperinsulinemia, however, the glucose infusion rate required was 4.15 +/- 0.39, 9.45 +/- 1.05, and 12.70 +/- 0.81 mg/kg X min at glucose levels of 90 +/- 1, 139 +/- 1, and 206 +/- 1 mg/dl, respectively. Lactate concentrations rose significantly during hyperglycemia, but the rise in the presence of increased insulin concentrations (from 0.72 +/- 0.06 to 1.31 +/- 0.11 mmol/liter; P less than 0.001) considerably exceeded the increment (from 0.74 +/- 0.05 to 0.92 +/- 0.03 mmol/liter) with basal insulin levels. While both FFA and glycerol concentrations were immediately reduced by euglycemic hyperinsulinemia, the fall in FFA during hyperglycemia in the presence of basal insulin levels preceded the decrease in glycerol concentrations by 45 min. Forearm oxygen consumption did not change throughout the study.(ABSTRACT TRUNCATED AT 400 WORDS)
我们通过测定在10名正常男性基础及升高的血清胰岛素浓度情况下,分级高血糖对外周葡萄糖摄取和全身代谢的影响,研究了高血糖对人体葡萄糖稳态的影响。这是通过在联合静脉输注生长抑素、胰高血糖素和胰岛素期间同时应用前臂和钳夹技术(正常血糖和高血糖)来实现的。在维持平均(±标准误)基础血清胰岛素水平(14±2微单位/毫升)的同时,空腹动脉血糖浓度从(90±1毫克/分升)升高至146±1和202±1毫克/分升(各持续120分钟),仅使前臂葡萄糖摄取(FGU)适度增加,分别从0.06±0.01增加至0.15±0.02,然后再增加至0.24±0.03毫克/100毫升前臂×分钟。在生理性高胰岛素血症(47±3微单位/毫升)期间,类似分级高血糖对FGU的影响显著增强。在血浆葡萄糖浓度为90±1、139±1和206±1毫克/分升时,FGU分别升至0.33±0.05、0.59±0.07和0.83±0.12毫克/100毫升前臂×分钟。在基础胰岛素水平下维持葡萄糖钳夹所需的葡萄糖输注速率在葡萄糖浓度为146±1和202±1毫克/分升时分别为1.08±0.20和2.67±0.39毫克/千克×分钟。然而,在生理性高胰岛素血症期间,在葡萄糖水平为90±1、139±1和206±1毫克/分升时,所需的葡萄糖输注速率分别为4.15±0.39、9.45±1.05和12.70±0.81毫克/千克×分钟。高血糖期间乳酸浓度显著升高,但在胰岛素浓度增加时的升高(从0.72±0.06至1.31±0.11毫摩尔/升;P<0.001)大大超过了基础胰岛素水平时的升高(从0.74±0.05至0.92±0.03毫摩尔/升)。虽然正常血糖高胰岛素血症会立即降低游离脂肪酸(FFA)和甘油浓度,但在基础胰岛素水平下高血糖期间FFA的下降比甘油浓度的下降提前45分钟。在整个研究过程中,前臂耗氧量没有变化。(摘要截短至400字)