Owen O E, Smalley K J, D'Alessio D A, Mozzoli M A, Dawson E K
Lankenau Hospital, Main Line Health, Jefferson Health System, Wynnewood, PA, USA.
Am J Clin Nutr. 1998 Jul;68(1):12-34. doi: 10.1093/ajcn/68.1.12.
The purpose of this work was to clarify the essentiality of glucose production from amino acids in obese subjects undergoing prolonged starvation and to provide an explanation for death after the depletion of lean body mass when some body fat is still available to meet body energy requirements. Five obese subjects fasted for 21 d. Nitrogen balance studies were combined with measurements of blood metabolite and hormone concentrations, indirect calorimetry, determination of body-composition changes, and catheterization techniques. Phenylacetate was administered from day 19 to day 21 to remove glutamine from the body and to assess this perturbation on energy requirements, ammoniagenesis, ureagenesis, gluconeogenesis, and ketogenesis. The obese subjects lost body fat and fat-free mass in parallel and resting metabolic energy requirements per mass remained constant during starvation. Urinary nitrogen excretion reflected continuous demands for amino acid oxidation. Phenylacetate administration decreased blood glutamine concentrations, increased plasma epinephrine concentrations, and increased urinary nitrogen loss through phenylacetylglutamine excretion; urinary excretion rates of urea, ammonium, urate, creatinine, and ketone bodies remained unchanged. The essentiality of amino acid oxidation was therefore shown. Late in prolonged starvation, aminogenic oxidation amounted to 7% and fat provided the remaining energy requirements. Hepatic and renal gluconeogenesis were not curtailed. Blood glutamate served as a vehicle for carbon and nitrogen transport; the contribution of glycerol to gluconeogenesis equaled that of all amino acids combined. The minimal quantities of amino acid (0.27 +/- 0.08 and 0.52 +/- 0.10 g) and fat (1.53 +/- 0.21 and 2.98 +/- 0.15 g) oxidized per kg body wt or fat-free mass/d, respectively, were determined. Included within amino acid and fat oxidation were the minimal amounts of precursors needed for synthesizing the essential quantity of glucose (0.34 +/- 0.14 and 0.66 +/- 0.20 g) oxidized per kg body wt or fat-free mass, respectively.
这项研究的目的是阐明长期饥饿的肥胖受试者中氨基酸生成葡萄糖的必要性,并解释在瘦体重消耗殆尽而仍有一些身体脂肪可满足身体能量需求时受试者死亡的原因。五名肥胖受试者禁食21天。氮平衡研究与血液代谢物和激素浓度测量、间接量热法、身体成分变化测定以及导管插入技术相结合。从第19天到第21天给予苯乙酸,以清除体内谷氨酰胺,并评估这种干扰对能量需求、氨生成、尿素生成、糖异生和酮生成的影响。肥胖受试者的身体脂肪和去脂体重平行减少,饥饿期间每单位质量的静息代谢能量需求保持恒定。尿氮排泄反映了对氨基酸氧化的持续需求。给予苯乙酸降低了血液谷氨酰胺浓度,增加了血浆肾上腺素浓度,并通过苯乙酰谷氨酰胺排泄增加了尿氮损失;尿素、铵、尿酸、肌酐和酮体的尿排泄率保持不变。因此显示了氨基酸氧化的必要性。在长期饥饿后期,氨基氧化占7%,脂肪提供其余的能量需求。肝脏和肾脏的糖异生并未减少。血液中的谷氨酸作为碳和氮运输的载体;甘油对糖异生的贡献与所有氨基酸的总贡献相当。分别测定了每千克体重或去脂体重每天氧化的氨基酸(0.27±0.08和0.52±0.10克)和脂肪(1.53±0.21和2.98±0.15克)的最小量。在氨基酸和脂肪氧化中包括合成每千克体重或去脂体重氧化的必需量葡萄糖(分别为0.34±0.14和0.66±0.20克)所需的最小量前体。