Kupfer S R, Underwood L E, Baxter R C, Clemmons D R
Department of Pediatrics, University of North Carolina School of Medicine, Chapel Hill 27599.
J Clin Invest. 1993 Feb;91(2):391-6. doi: 10.1172/JCI116212.
The use of growth hormone (GH) as an anabolic agent is limited by its tendency to cause hyperglycemia and by its inability to reverse nitrogen wasting in some catabolic conditions. In a previous study comparing the anabolic actions of GH and IGF-I (insulin-like growth factor I), we observed that intravenous infusions of IGF-I (12 micrograms/kg ideal body wt [IBW]/h) attenuated nitrogen wasting to a degree comparable to GH given subcutaneously at a standard dose of 0.05 mg/kg IBW per d. IGF-I, however, had a tendency to cause hypoglycemia. In the present study, we treated seven calorically restricted (20 kcal/kg IBW per d) normal volunteers with a combination of GH and IGF-I (using the same doses as in the previous study) and compared its effects on anabolism and carbohydrate metabolism to treatment with IGF-I alone. The GH/IGF-I combination caused significantly greater nitrogen retention (262 +/- 43 mmol/d, mean +/- SD) compared to IGF-I alone (108 +/- 29 mmol/d; P < 0.001). GH/IGF-I treatment resulted in substantial urinary potassium conservation (34 +/- 3 mmol/d, mean +/- SE; P < 0.001), suggesting that most protein accretion occurred in muscle and connective tissue. GH attenuated the hypoglycemia induced by IGF-I as indicated by fewer hypoglycemic episodes and higher capillary blood glucose concentrations on GH/IGF-I (4.3 +/- 1.0 mmol/liter, mean +/- SD) compared to IGF-I alone (3.8 +/- 0.8 mmol/liter; P < 0.001). IGF-I caused a marked decline in C-peptide (1,165 +/- 341 pmol/liter; mean +/- SD) compared to the GH/IGF-I combination (2,280 +/- 612 pmol/liter; P < 0.001), suggesting maintenance of normal carbohydrate metabolism with the latter regimen. GH/IGF-I produced higher serum IGF-I concentrations (1,854 +/- 708 micrograms/liter; mean +/- SD) compared to IGF-I only treatment (1,092 +/- 503 micrograms/liter; P < 0.001). This observation was associated with increased concentrations of IGF binding protein 3 and acid-labile subunit on GH/IGF-I treatment and decreased concentrations on IGF-I alone. These results suggest that the combination of GH and IGF-I treatment is substantially more anabolic than either IGF-I or GH alone. GH/IGF-I treatment also attenuates the hypoglycemia caused by IGF-I alone. GH/IGF-I treatment could have important applications in diseases associated with catabolism.
生长激素(GH)作为一种合成代谢剂的应用受到其导致高血糖倾向以及在某些分解代谢状态下无法逆转氮消耗的限制。在先前一项比较GH和IGF-I(胰岛素样生长因子I)合成代谢作用的研究中,我们观察到静脉输注IGF-I(12微克/千克理想体重[IBW]/小时)可将氮消耗减轻至与皮下注射标准剂量0.05毫克/千克IBW每日的GH相当的程度。然而,IGF-I有导致低血糖的倾向。在本研究中,我们用GH和IGF-I的组合(使用与先前研究相同的剂量)治疗了7名热量受限(每日20千卡/千克IBW)的正常志愿者,并将其对合成代谢和碳水化合物代谢的影响与单独使用IGF-I治疗进行比较。与单独使用IGF-I(108±29毫摩尔/天)相比,GH/IGF-I组合导致显著更高的氮潴留(262±43毫摩尔/天,均值±标准差;P<0.001)。GH/IGF-I治疗导致大量尿钾潴留(34±3毫摩尔/天,均值±标准误;P<0.001),这表明大部分蛋白质积累发生在肌肉和结缔组织中。与单独使用IGF-I(3.8±0.8毫摩尔/升)相比,GH减轻了IGF-I诱导的低血糖,表现为GH/IGF-I治疗时低血糖发作次数减少且毛细血管血糖浓度更高(4.3±1.0毫摩尔/升,均值±标准差;P<0.001)。与GH/IGF-I组合(2280±612皮摩尔/升;P<0.001)相比,IGF-I导致C肽显著下降(1165±341皮摩尔/升;均值±标准差),这表明后一种方案维持了正常的碳水化合物代谢。与仅使用IGF-I治疗(1092±503微克/升)相比,GH/IGF-I产生更高的血清IGF-I浓度(1854±708微克/升;均值±标准差;P<0.001)。这一观察结果与GH/IGF-I治疗时IGF结合蛋白3和酸不稳定亚基浓度增加以及单独使用IGF-I时浓度降低有关。这些结果表明,GH和IGF-I联合治疗的合成代谢作用比单独使用IGF-I或GH要强得多。GH/IGF-I治疗还减轻了单独使用IGF-I引起的低血糖。GH/IGF-I治疗可能在与分解代谢相关的疾病中有重要应用。