Cherruau B, Mangeot M, Demelier J F, Charpentier C, Pelletier C, Lemonnier A
Nutr Metab. 1980;24(6):367-82.
Biotin deficiency induced in the rat, with a biotin-deficient diet but with added avidin involves clinical symptoms of deficiency as well as an important drop (80%) in propionyl-CoA carboxylase activity in the liver, heart and kidneys. But major biochemical anomalies (ketoacidosis and increased urinary elimination of propionic acid), characteristic of propionic acidaemia due to propionyl-CoA carboxylase deficiency in man, are not observed in the rat. Nevertheless, abnormal urinary elimination of methylcitrate and tiglylglycine reflects an appreciable decrease in the metabolism of propionyl-CoA in these animals. The propionyl-CoA load caused by the administration of metabolic precursors of this substance, mainly L-isoleucine, does not induce important biochemical variations except for excretion of propionylglycine.
用缺乏生物素但添加抗生物素蛋白的饮食诱导大鼠出现生物素缺乏,会引发缺乏症的临床症状,以及肝脏、心脏和肾脏中丙酰辅酶A羧化酶活性大幅下降(80%)。但是,人类因丙酰辅酶A羧化酶缺乏导致丙酸血症的主要生化异常(酮症酸中毒和尿中丙酸排泄增加)在大鼠中并未观察到。然而,尿中柠檬酸甲酯和惕各酰甘氨酸的异常排泄反映出这些动物体内丙酰辅酶A代谢明显减少。由该物质的代谢前体(主要是L-异亮氨酸)给药引起的丙酰辅酶A负荷,除了丙酰甘氨酸排泄外,不会引起重要的生化变化。