Stevenson R W, Steiner K E, Connolly C C, Fuchs H, Alberti K G, Williams P E, Cherrington A D
Department of Molecular Physiology and Biophysics, Vanderbilt University School of Medicine, Nashville, Tennessee 37232-0615.
Am J Physiol. 1991 Mar;260(3 Pt 1):E363-70. doi: 10.1152/ajpendo.1991.260.3.E363.
The effects of increases in plasma epinephrine from 78 +/- 32 to 447 +/- 75, 1,812 +/- 97, or 2,495 +/- 427 pg/ml on glucose production, including gluconeogenesis, were determined in the conscious, overnight-fasted dog, using a combination of tracer [( 3-3H]glucose and [U-14C]alanine) and arteriovenous difference techniques. Insulin and glucagon were fixed at basal levels using a pancreatic clamp. Plasma glucose levels rose during the 180-min epinephrine infusion by 47 +/- 7, 42 +/- 22, and 74 +/- 25 mg/dl, respectively, in association with increases in hepatic glucose output of 1.04 +/- 0.22, 1.87 +/- 0.23, and 3.70 +/- 0.83 mg.kg-1.min-1 (at 15 min). Blood lactate levels rose by 1.52 +/- 0.24, 4.29 +/- 0.49, and 4.60 +/- 0.45 mmol/l, respectively, by 180 min, despite increases in hepatic uptake of lactate of 3.47 +/- 5.73, 12.83 +/- 3.46, and 37.00 +/- 4.20 mumol.kg-1.min-1. The intrahepatic gluconeogenic efficiency with which the liver converted the incoming alanine to glucose had risen by 84 +/- 40, 77 +/- 24, and 136 +/- 34% at 180 min, respectively. The latter effect plus the effect on net hepatic lactate uptake point to an intrahepatic action of high levels of the hormone in vivo. In conclusion, epinephrine produces dose-dependent increments in overall glucose production, which involve a progressive stimulation of both glycogenolysis (as assessed by glucose production at 15 min) and gluconeogenesis (assessed in the last 30 min of the study). The latter involves a peripheral action of the catecholamine to increase gluconeogenic substrate supply to the liver and may also involve a hepatic effect when high epinephrine levels are present.
在清醒、禁食过夜的犬中,采用示踪剂([3-3H]葡萄糖和[U-14C]丙氨酸)与动静脉差技术相结合的方法,测定血浆肾上腺素从78±32 pg/ml增加到447±75 pg/ml、1812±97 pg/ml或2495±427 pg/ml对葡萄糖生成(包括糖异生)的影响。使用胰腺钳将胰岛素和胰高血糖素固定在基础水平。在180分钟肾上腺素输注期间,血浆葡萄糖水平分别升高47±7、42±22和74±25 mg/dl,同时肝葡萄糖输出在15分钟时分别增加1.04±0.22、1.87±0.23和3.70±0.83 mg·kg-1·min-1。到180分钟时,血乳酸水平分别升高1.52±0.24、4.29±0.49和4.60±0.45 mmol/l,尽管肝乳酸摄取分别增加3.47±5.73、12.83±3.46和37.00±4.20 μmol·kg-1·min-1。在180分钟时,肝脏将输入的丙氨酸转化为葡萄糖的肝内糖异生效率分别提高了84±40%、77±24%和136±34%。后一种效应加上对肝净乳酸摄取的影响表明该激素在体内对肝脏有作用。总之,肾上腺素使总体葡萄糖生成呈剂量依赖性增加,这涉及对糖原分解(通过15分钟时的葡萄糖生成评估)和糖异生(在研究的最后30分钟评估)的逐步刺激。后者涉及儿茶酚胺的外周作用,以增加肝脏的糖异生底物供应,当肾上腺素水平较高时也可能涉及肝脏效应。