Yudkoff M, Daikhin Y, Ye X, Wilson J M, Batshaw M L
Department of Pediatrics, University of Pennsylvania School of Medicine, Philadelphia, USA.
J Inherit Metab Dis. 1998;21 Suppl 1:21-9. doi: 10.1023/a:1005345205403.
We have utilized stable isotopes to measure in vivo rates of ureagenesis. In one testing procedure, 15NH4Cl was administered orally to controls and to heterozygotes for ornithine transcarbamylase deficiency. Controls produced [15N]urea at a rate that was greater than that of symptomatic carriers, but indistinguishable from that of asymptomatic carriers. In contrast, both symptomatic and asymptomatic heterozygotes produced [5-15N]glutamine more rapidly than the controls. Ureagenesis could also be measured by administering sodium [1-13C]acetate to a healthy adult and measuring subsequent formation of [13C]urea. The latter approach involves the use of isotope ratio mass spectrometry to determine isotopic abundance. This technique is much more sensitive than gas chromatography-mass spectrometry for the measurement of isotopic label, a consideration that makes the method more suitable for the study of subjects in whom ureagenesis is severely compromised, for example the human male neonate with a near complete deficiency of ornithine transcarbamylase.
我们利用稳定同位素来测量体内尿素生成的速率。在一个测试程序中,向鸟氨酸转氨甲酰酶缺乏症的对照者和杂合子口服15NH4Cl。对照者产生[15N]尿素的速率高于有症状携带者,但与无症状携带者无法区分。相比之下,有症状和无症状的杂合子产生[5-15N]谷氨酰胺的速度都比对照者快。也可以通过向一名健康成年人施用[1-13C]醋酸钠并测量随后[13C]尿素的形成来测量尿素生成。后一种方法涉及使用同位素比率质谱法来确定同位素丰度。对于测量同位素标记,该技术比气相色谱-质谱法灵敏得多,这一因素使得该方法更适合于研究尿素生成严重受损的受试者,例如鸟氨酸转氨甲酰酶几乎完全缺乏的人类男性新生儿。