Keller U, Schnell H, Girard J, Stauffacher W
Diabetologia. 1984 Feb;26(2):103-8. doi: 10.1007/BF00281115.
The effect of physiological elevation of growth hormone levels on ketone body kinetics was determined using a 14C-ketone body tracer technique in normal and acutely insulin-deficient man. Changes of ketone body production and metabolic clearance rates during growth hormone infusion (plasma levels of approximately 25 micrograms/1) were measured during basal conditions and during heparin-induced elevation of non-esterified fatty acid levels. Growth hormone administration to six subjects fasted overnight resulted in an increase in ketone body production which exceeded that observed in nine control subjects (5.5 +/- 0.5 versus 3.1 +/- 0.1 mumol X kg-1 X min-1, p less than 0.025) after elevation of plasma non-esterified fatty acids. Growth hormone infusion increased glycerol and non-esterified fatty acid concentrations indicating enhanced lipolysis. During somatostatin-induced acute insulin deficiency (n = 7), growth hormone enhanced the increase in total ketone body production observed in six subjects receiving somatostatin alone (8.4 +/- 0.8 versus 4.1 +/- 0.7 mumol X kg-1 X min-1, p less than 0.01). Total ketone body metabolic clearance decreased by 50% during somatostatin and remained uninfluenced by growth hormone. Non-esterified fatty acids and glycerol levels increased during somatostatin, and growth hormone failed to alter non-esterified fatty acid levels significantly. The results demonstrate a stimulatory effect of high physiological growth hormone levels on ketogenesis which is largely explained by an enhancement of lipolysis and thus increase in substrate supply for ketogenesis. Growth hormone administration during acute insulin deficiency enhanced ketogenesis in the absence of alterations in plasma non-esterified fatty acid levels, suggesting a direct hepatic ketogenic effect.
采用14C-酮体示踪技术,在正常人和急性胰岛素缺乏的男性中,测定了生长激素水平生理性升高对酮体动力学的影响。在基础状态以及肝素诱导非酯化脂肪酸水平升高期间,测量了生长激素输注(血浆水平约为25微克/升)过程中酮体生成和代谢清除率的变化。对6名过夜禁食的受试者给予生长激素,导致酮体生成增加,在血浆非酯化脂肪酸升高后,这种增加超过了9名对照受试者的观察值(5.5±0.5对3.1±0.1微摩尔·千克-1·分钟-1,p<0.025)。生长激素输注增加了甘油和非酯化脂肪酸浓度,表明脂解增强。在生长抑素诱导的急性胰岛素缺乏期间(n=7),生长激素增强了6名单独接受生长抑素的受试者中观察到的总酮体生成增加(8.4±0.8对4.1±0.7微摩尔·千克-1·分钟-1,p<0.01)。在生长抑素作用期间,总酮体代谢清除率下降了50%,且不受生长激素影响。生长抑素作用期间非酯化脂肪酸和甘油水平升高,生长激素未能显著改变非酯化脂肪酸水平。结果表明,高生理性生长激素水平对酮体生成有刺激作用,这在很大程度上是由脂解增强所解释的,从而增加了酮体生成的底物供应。在急性胰岛素缺乏期间给予生长激素,在血浆非酯化脂肪酸水平无改变的情况下增强了酮体生成,提示有直接的肝脏生酮作用。