Arnal M, Obled C, Attaix D, Patureau-Mirand P, Bonin D
Laboratoire d'étude du Métabolisme Azoté, CRZV-INRA-Thiex, Ceyrat, France.
Diabete Metab. 1987 Nov-Dec;13(6):630-42.
The balance between protein synthesis and breakdown (protein turnover) regulates whole-body protein mass. The relationships between dietary changes (amount and composition of food) and protein synthesis, protein breakdown and amino acid oxidation have been explored in order to better understand adaptations of protein and amino acid metabolism. Methods for measuring protein synthesis, especially whole-body protein synthesis, can be divided into two groups: the 15N end-product method (urea and/or ammonia), and the incorporation of labelled amino acid(s) into proteins. Assumptions and limitations of the widely used two-pool model (free amino acid and protein pools) are discussed. Results obtained with different methods and for amino acids have been compared, to assess their ability to detect changes in protein synthesis rates. Methods of measuring protein breakdown have also been described briefly. Food intake affects whole-body and tissue protein turnover throughout development of animals and humans in different ways. Protein metabolism fluctuates during the 24-hour period in response to intermittent food intake. During the post-prandial period, a net whole-body protein deposition occurs. This is essentially due to increased protein synthesis. The free amino acid pool and amino acid oxidation rates also increase. Consequently, amino acids are used to a great extent as energy substrates. In contrast, a decrease in protein breakdown could enhance protein deposition. During fasting, the rates of whole-body protein synthesis are lower than those of protein breakdown. This results in protein loss, essentially because the drop in protein synthesis rate in muscle is pronounced. N balance is controlled by the amounts and composition of the diet and by changes in protein synthesis and breakdown. Increasing food intake above levels of energy equilibrium can produce growth by enhancing both the whole-body protein synthesis and breakdown rates. Below energy equilibrium, whole-body protein loss occurs because of decreased protein synthesis which becomes lower than protein breakdown. Protein synthesis rate is the main factor controlling N balance in response to alterations in food intake. Increasing dietary protein, especially the essential amino acids, involves increased rates of whole-body protein synthesis and breakdown. The improved N balance obtained by enhancing dietary non-protein energy (carbohydrate, fat) can be brought on by reducing amino acid oxidation and slightly increasing protein synthesis. The effects of dietary protein and energy on protein turnover are apparently additive.
蛋白质合成与分解之间的平衡(蛋白质周转)调节着全身蛋白质总量。人们对饮食变化(食物的量和组成)与蛋白质合成、蛋白质分解及氨基酸氧化之间的关系进行了探索,以便更好地理解蛋白质和氨基酸代谢的适应性变化。测量蛋白质合成的方法,尤其是全身蛋白质合成的方法,可分为两类:15N终产物法(尿素和/或氨),以及将标记氨基酸掺入蛋白质中。讨论了广泛使用的双池模型(游离氨基酸池和蛋白质池)的假设和局限性。比较了用不同方法获得的结果以及针对氨基酸的结果,以评估它们检测蛋白质合成速率变化的能力。还简要描述了测量蛋白质分解的方法。在动物和人类的整个发育过程中,食物摄入以不同方式影响全身和组织的蛋白质周转。由于间歇性进食,蛋白质代谢在24小时内会发生波动。在餐后期间,会出现全身蛋白质的净沉积。这主要是由于蛋白质合成增加所致。游离氨基酸池和氨基酸氧化速率也会增加。因此,氨基酸在很大程度上被用作能量底物。相反,蛋白质分解的减少可能会增强蛋白质沉积。在禁食期间,全身蛋白质合成速率低于蛋白质分解速率。这会导致蛋白质流失,主要是因为肌肉中蛋白质合成速率的下降很明显。氮平衡受饮食的量和组成以及蛋白质合成和分解变化的控制。将食物摄入量增加到能量平衡水平以上可通过提高全身蛋白质合成和分解速率来促进生长。低于能量平衡水平时,由于蛋白质合成减少且低于蛋白质分解,会出现全身蛋白质流失。蛋白质合成速率是响应食物摄入量变化控制氮平衡的主要因素。增加膳食蛋白质,尤其是必需氨基酸,会导致全身蛋白质合成和分解速率增加。通过增加膳食非蛋白质能量(碳水化合物、脂肪)获得的改善的氮平衡,可以通过减少氨基酸氧化并略微增加蛋白质合成来实现。膳食蛋白质和能量对蛋白质周转的影响显然是相加的。