Walter J H, Thompson G N, Leonard J V, Bartlett K, Halliday D
Department of Child Health, Institute of Child Health, London.
Lancet. 1989 Jun 10;1(8650):1298-9. doi: 10.1016/s0140-6736(89)92689-5.
The rates of propionate production and aminoacid catabolism in 5 children with methylmalonic acidaemia were measured by use of stable isotope techniques. Total propionate production was 55-186 mumol/kg per h, to which the maximum contribution of protein catabolism was 10-35 mumol/kg per h (5-40%). These findings indicate important sources of propionate other than protein catabolism, which may account for the limited efficacy of dietary protein restriction in treatment of methylmalonic acidaemia.
采用稳定同位素技术测定了5例甲基丙二酸血症患儿的丙酸生成率和氨基酸分解代谢率。总丙酸生成量为每小时55 - 186微摩尔/千克,其中蛋白质分解代谢的最大贡献为每小时10 - 35微摩尔/千克(5% - 40%)。这些发现表明,除蛋白质分解代谢外,还有其他重要的丙酸来源,这可能解释了饮食蛋白质限制在治疗甲基丙二酸血症中疗效有限的原因。