谷氨酰胺合成酶
谷氨酰胺
尿素循环
高氨血症
谷氨酰胺酶
谷氨酸脱氢酶
尿素
去酰胺
生物化学
内科学
氨
鸟氨酸转氨酶
化学
分解代谢
内分泌学
酪氨酸转氨酶
生物
新陈代谢
酶
氨基酸
谷氨酸受体
酶诱导剂
医学
精氨酸
受体
作者
Theodorus B. M. Hakvoort,Youji He,Wim Kulik,Jacqueline L.M. Vermeulen,Suzanne Duijst,Jan M. Ruijter,Jurgen H. Runge,Nicolaas E.P. Deutz,S. Eleonore Koehler,Wouter H. Lamers
出处
期刊:Hepatology
[Lippincott Williams & Wilkins]
日期:2016-09-19
卷期号:65 (1): 281-293
被引量:153
摘要
Hepatic GS contributes to both enteral and systemic ammonia detoxification. Glutamine synthesis in the periphery (including that in pericentral hepatocytes) and glutamine catabolism in (periportal) hepatocytes represents the high-affinity ammonia-detoxifying system of the body. The dependence of glutamine-bound ammonia disposal to urea on the rate of glutamine synthesis suggests that enhancing peripheral glutamine synthesis is a promising strategy to treat hyperammonemia. Because total urea synthesis does not depend on glutamine synthesis, we hypothesize that glutamate dehydrogenase complements mitochondrial ammonia production. (Hepatology 2017;65:281-293).
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