alpha-Ketoglutaramate: an overlooked metabolite of glutamine and a biomarker for hepatic encephalopathy and inborn errors of the urea cycle

作者：Cooper Arthur J L^*; Kuhara Tomiko

来源：Metabolic Brain Disease, 2014, 29(4): 991-1006.

DOI：10.1007/s11011-013-9444-9

• omega-Amidase
• Ammonia
• GlutaminaseII
• Hepatic encephalopathy
• alpha-ketoglutaramate
• Urea cycle disorders

Glutamine metabolism is generally regarded as proceeding via glutaminase-catalyzed hydrolysis to glutamate and ammonia, followed by conversion of glutamate to alpha-ketoglutarate catalyzed by glutamate dehydrogenase or by a glutamate-linked aminotransferase (transaminase). However, another pathway exists for the conversion of glutamine to alpha-ketoglutarate that is often overlooked, but is widely distributed in nature. This pathway, referred to as the glutaminase II pathway, consists of a glutamine transaminase coupled to omega-amidase. Transamination of glutamine results in formation of the corresponding alpha-keto acid, namely, alpha-ketoglutaramate (KGM). KGM is hydrolyzed by omega-amidase to aketoglutarate and ammonia. The net glutaminase II reaction is: L-Glutamine+alpha-keto acid+H2O -%26gt; alpha-ketoglutarate+L-amino acid+ammonia. In this mini-review the biochemical importance of the glutaminase II pathway is summarized, with emphasis on the key component KGM. Forty years ago it was noted that the concentration of KGM is increased in the cerebrospinal fluid (CSF) of patients with hepatic encephalopathy (HE) and that the level of KGMin the CSF correlates well with the degree of encephalopathy. In more recent work, we have shown that KGM is markedly elevated in the urine of patients with inborn errors of the urea cycle. It is suggested that KGM may be a useful biomarker for many hyperammonemic diseases including hepatic encephalopathy, inborn errors of the urea cycle, citrin deficiency and lysinuric protein intolerance.

• 出版日期2014-12