Gibson N R, Fereday A, Cox M, Halliday D, Pacy P J, Millward D J
Center for Nutrition and Food Safety, School of Biological Sciences, University of Surrey, Guildford, United Kingdom.
Am J Physiol. 1996 Feb;270(2 Pt 1):E282-91. doi: 10.1152/ajpendo.1996.270.2.E282.
Ten adult men were infused with L-[1-13C]leucine for 9 h commencing in the postabsorptive state (PA, 0-3 h), during the half-hourly feeding of low-protein meals (LP, protein = 2% calories, 3-6 h), and during feeding isoenergetic high-protein meals (HP, protein = 14% calories, 6-9 h). Leucine oxidation and turnover (protein synthesis and degradation) were determined from plasma alpha-[1-13C]ketoisocaproate enrichment and expired 13CO2 excretion measured during the third hour of each 3-h period. Plasma insulin increased markedly with feeding to a level that was maintained with both diets. The negative postabsorptive leucine balance became less negative during the LP meals (P < 0.01) and was positive with the HP meals (P < 0.01). The significant responses to feeding (all P < 0.01) were for oxidation -13% (PA-LP), +50% (LP-HP), and +29% (PA-HP); for degradation -24% (PA-LP), -30% (LP-HP), and -47% (PA-HP); and for synthesis -14% (PA-LP), +29% (LP-HP), and +11% (PA-HP). These data support a feeding mechanism involving both an insulin-mediated, protein-conserving influence of dietary energy that inhibits degradation, lowers amino acid levels, and reduces oxidation, and amino acid-mediated augmentation of the inhibition of degradation, a stimulation of synthesis, and an increase in oxidation when leucine dietary supply exceeds the capacity for its net deposition.
十名成年男性在空腹状态(PA,0 - 3小时)开始接受9小时的L-[1-13C]亮氨酸输注,期间每半小时喂食低蛋白餐(LP,蛋白质含量为2%卡路里,3 - 6小时),以及喂食等能量的高蛋白餐(HP,蛋白质含量为14%卡路里,6 - 9小时)。亮氨酸氧化和周转率(蛋白质合成与降解)通过在每个3小时时间段的第三个小时测量血浆α-[1-13C]酮异己酸富集和呼出的13CO2排泄量来确定。喂食后血浆胰岛素显著升高至两种饮食均维持的水平。空腹状态下的负亮氨酸平衡在低蛋白餐期间变得不那么负(P < 0.01),而在高蛋白餐时变为正(P < 0.01)。对喂食的显著反应(所有P < 0.01)为氧化方面 -13%(PA - LP)、+50%(LP - HP)和 +29%(PA - HP);降解方面 -24%(PA - LP)、-30%(LP - HP)和 -47%(PA - HP);合成方面 -14%(PA - LP)、+29%(LP - HP)和 +11%(PA - HP)。这些数据支持一种进食机制,该机制涉及饮食能量的胰岛素介导的蛋白质保护作用,其抑制降解、降低氨基酸水平并减少氧化,以及当亮氨酸饮食供应超过其净沉积能力时,氨基酸介导的对降解抑制的增强、合成的刺激和氧化的增加。