Weijs P J, Calder A G, Milne E, Lobley G E
Rowett Research Institute, Bucksburn, Aberdeen.
Br J Nutr. 1996 Oct;76(4):491-9. doi: 10.1079/bjn19960058.
Hepatic NH3 detoxification by ureagenesis requires an input of aspartate-N, originating either from amino acid-N or NH3-N. The relative importance of these two routes may depend on the nutritional state. To test this, four volunteers were given a liquid diet for 2 d and then on day 3 were either fed every 20 min or fasted. Doses of 15NH4Cl were taken orally every 20 min for 6 h (total 1.5 g) and blood was sampled hourly. Urea-N elimination under fasted conditions was only 0.75 of that for the fed state. Considering the increase in body urea pool during feeding, ureagenesis during fasting was probably closer to 0.6 of that during feeding. Since the [14N15N]urea enrichment was not different between the fed and fasted states, the proportion of the 15NH3 dose converted to urea during fasting was also 0.6 of that during the fed condition. No change in [14N15N]urea and [amide-15N]glutamine enrichment suggested that NH3 enrichment was also not affected by nutritional state. Enrichment of [15N15N]urea was approximately 0.05 that of [14N15N]urea which indicates that 15NH3 can also enter the aspartate route, the importance of which is yet unknown. Both [15N15N]urea and [amino-15N]glutamine enrichment in the fasted state were approximately 1.7 times that in the fed state, indicating increased labelling of precursors and/or increased NH3 flux through the aspartate route. Glutamate, valine, leucine and isoleucine showed comparable increases in enrichment during fasting. Arginine enrichment was unaltered by nutritional state, but was lower than [14N15N]urea, indicating incomplete equilibration with the arginine pool in periportal hepatocytes. The present study indicates that hepatic NH3 detoxification may use the aspartate route, gaining importance in the fasted state. The majority of urea was supplied with only one N atom from NH3, thus provision of the other may have consequences for alternative substrates, in particular amino acids.
通过尿素生成进行肝脏氨解毒需要输入天冬氨酸 -N,其来源可以是氨基酸 -N 或氨 -N。这两条途径的相对重要性可能取决于营养状态。为了验证这一点,让四名志愿者食用流食两天,然后在第三天,一部分人每20分钟进食一次,另一部分人禁食。每20分钟口服一次15NH4Cl,持续6小时(总量1.5克),并每小时采集一次血液样本。禁食条件下尿素 -N 的消除量仅为进食状态下的0.75倍。考虑到进食期间体内尿素池的增加,禁食期间的尿素生成量可能更接近进食期间的0.6倍。由于进食和禁食状态下[14N15N]尿素的富集程度没有差异,禁食期间转化为尿素的15NH3剂量比例也是进食状态下的0.6倍。[14N15N]尿素和[酰胺 -15N]谷氨酰胺的富集程度没有变化,这表明氨的富集程度也不受营养状态的影响。[15N15N]尿素的富集程度约为[14N15N]尿素的0.05倍,这表明15NH3也可以进入天冬氨酸途径,但其重要性尚不清楚。禁食状态下[15N15N]尿素和[氨基 -15N]谷氨酰胺的富集程度约为进食状态下的1.7倍,这表明前体的标记增加和/或通过天冬氨酸途径的氨通量增加。谷氨酸、缬氨酸、亮氨酸和异亮氨酸在禁食期间的富集程度有类似的增加。精氨酸的富集程度不受营养状态的影响,但低于[14N15N]尿素,这表明与门静脉周围肝细胞中的精氨酸池未完全平衡。本研究表明,肝脏氨解毒可能利用天冬氨酸途径,在禁食状态下变得更加重要。大多数尿素仅从氨中获得一个氮原子,因此提供另一个氮原子可能会对替代底物,特别是氨基酸产生影响。