Keller U, Schnell H, Sonnenberg G E, Gerber P P, Stauffacher W
Diabetes. 1983 May;32(5):387-91. doi: 10.2337/diab.32.5.387.
To assess the role of endogenous glucagon in regulating hepatic ketone body production in ketotic insulin-withdrawn diabetic subjects, ketone body kinetics were determined in two groups of C-peptide-negative diabetics 6 h after interruption of a s.c. insulin infusion. In group 1 (N = 5), glucagon levels were suppressed by infusion of somatostatin (SRIF), whereas in group 2 (N = 6) glucagon was replaced during SRIF by infusing glucagon at 2 ng/kg/min. Ketone body production rates as determined by primed-continuous infusion of [3-14C]acetoacetate declined from 19.5 +/- 0.8 to 16.4 +/- 0.4 mumol/kg/min (P less than 0.01) during 105 min of SRIF-induced glucagon suppression, whereas they remained unchanged (+0.2 +/- 0.4 mumol/kg/min, P less than 0.01 compared with SRIF) during glucagon replacement. Total ketone body concentrations remained unchanged during SRIF infusion but increased from 2.2 +/- 0.3 to 2.9 +/- 0.2 mmol/L (P less than 0.01) during glucagon replacement. The metabolic clearance rate of total ketone bodies declined significantly (P less than 0.01) by 27% and 21% in the two groups. Plasma free fatty acid and glycerol concentrations remained unchanged in both groups whereas plasma glucose decreased by 3.2 +/- 0.5 mmol/L during SRIF (P less than 0.01). Thus, endogenous glucagon contributed significantly to the maintenance of ketone body production rates in ketotic insulin-deficient diabetics. Since ketogenesis was altered in the absence of changes in free fatty acid levels, the results suggested that glucagon enhanced ketogenesis by an intrahepatic effect.
为评估内源性胰高血糖素在酮症性胰岛素停用的糖尿病患者中调节肝脏酮体生成的作用,在皮下胰岛素输注中断6小时后,对两组C肽阴性糖尿病患者进行了酮体动力学测定。在第1组(N = 5)中,通过输注生长抑素(SRIF)抑制胰高血糖素水平,而在第2组(N = 6)中,在SRIF期间以2 ng/kg/min的速度输注胰高血糖素以替代胰高血糖素。在SRIF诱导的胰高血糖素抑制的105分钟内,通过[3-14C]乙酰乙酸的首剂-连续输注测定的酮体生成率从19.5±0.8降至16.4±0.4 μmol/kg/min(P<0.01),而在胰高血糖素替代期间酮体生成率保持不变(+0.2±0.4 μmol/kg/min,与SRIF相比P<0.01)。在SRIF输注期间总酮体浓度保持不变,但在胰高血糖素替代期间从2.2±0.3增加到2.9±0.2 mmol/L(P<0.01)。两组中总酮体的代谢清除率均显著下降(P<0.01),分别下降27%和21%。两组血浆游离脂肪酸和甘油浓度均保持不变,而在SRIF期间血浆葡萄糖下降3.2±0.5 mmol/L(P<0.01)。因此,内源性胰高血糖素对酮症性胰岛素缺乏的糖尿病患者酮体生成率的维持有显著贡献。由于在游离脂肪酸水平无变化的情况下酮体生成发生改变,结果提示胰高血糖素通过肝内效应增强了酮体生成。