Jahoor Farook, Badaloo Asha, Villalpando Salvador, Reid Marvin, Forrester Terrence
US Department of Agriculture/Agricultural Research Service, Children's Nutrition Research Center, Department of Pediatrics, Baylor College of Medicine, Houston, TX 77030-2600, USA.
Am J Clin Nutr. 2007 Oct;86(4):1024-31. doi: 10.1093/ajcn/86.4.1024.
Although nutritionally dispensable amino acids are not essential in the diet, adequate synthesis is necessary for maintenance of good health. Whereas children with edematous severe childhood undernutrition (SCU) can maintain production rates of glycine and serine despite a slower body protein breakdown rate, it is unknown whether the same is true for the semidispensable amino acid arginine.
We aimed to measure arginine flux and intravascular nitric oxide synthesis in children with SCU.
Arginine flux and the fractional and absolute synthesis rates of plasma nitrite plus nitrate were measured postabsorptively by using a 6-h infusion of [(15)N(2)]-arginine in 2 groups of children with edematous (n = 14) or nonedematous (n = 7) SCU when they were infected and malnourished (postadmission day approximately 3; clinical phase 1), when they were no longer infected (postadmission day approximately 15; clinical phase 2), and when they were recovered (postadmission day approximately 55; clinical phase 3).
Arginine flux was slower (P < 0.01) and plasma arginine concentrations were lower in the edematous group than in the nonedematous group at clinical phase 1. At clinical phase 2, flux doubled to a value that was not significantly different from the value at clinical phase 3. There were no significant differences in the plasma concentration or fractional or absolute synthesis rate of plasma nitrite plus nitrate between the groups at any clinical phase and among clinical phases within each group.
Whereas children with nonedematous SCU can maintain arginine flux at the same rate as when recovered, children with edematous SCU cannot. The slower arginine flux was not, however, associated with slower nitric oxide synthesis.
尽管营养上非必需氨基酸在饮食中并非必不可少,但充足的合成对于维持良好健康是必要的。患有水肿型重度儿童营养不良(SCU)的儿童尽管身体蛋白质分解速率较慢,但仍能维持甘氨酸和丝氨酸的产生率,而对于半必需氨基酸精氨酸是否同样如此尚不清楚。
我们旨在测量SCU儿童的精氨酸通量和血管内一氧化氮合成。
在两组患有水肿(n = 14)或非水肿(n = 7)SCU的儿童感染并营养不良时(入院后约3天;临床阶段1)、不再感染时(入院后约15天;临床阶段2)以及康复时(入院后约55天;临床阶段3),通过6小时输注[(15)N(2)]-精氨酸,吸收后测量精氨酸通量以及血浆亚硝酸盐加硝酸盐的分数合成率和绝对合成率。
在临床阶段1,水肿组的精氨酸通量较慢(P < 0.01),血浆精氨酸浓度低于非水肿组。在临床阶段2,通量增加一倍,达到与临床阶段3的值无显著差异的水平。在任何临床阶段,两组之间以及每组内各临床阶段之间,血浆亚硝酸盐加硝酸盐的血浆浓度、分数合成率或绝对合成率均无显著差异。
非水肿型SCU儿童能够以与康复时相同的速率维持精氨酸通量,而水肿型SCU儿童则不能。然而,精氨酸通量较慢与一氧化氮合成较慢无关。