Disorders of glutamate metabolism

✍ Scribed by Kelly, Andrea ;Stanley, Charles A.

• Publisher: John Wiley and Sons
• Year: 2001
• Tongue: English
• Weight: 284 KB
• Volume: 7
• Category: Article
• ISSN: 1080-4013
• DOI: 10.1002/mrdd.1040

✦ Synopsis

Abstract

The significant role the amino acid glutamate assumes in a number of fundamental metabolic pathways is becoming better understood. As a central junction for interchange of amino nitrogen, glutamate facilitates both amino acid synthesis and degradation. In the liver, glutamate is the terminus for release of ammonia from amino acids, and the intrahepatic concentration of glutamate modulates the rate of ammonia detoxification into urea. In pancreatic β‐cells, oxidation of glutamate mediates amino acid‐stimulated insulin secretion. In the central nervous system, glutamate serves as an excitatory neurotransmittor. Glutamate is also the precursor of the inhibitory neurotransmittor GABA, as well as glutamine, a potential mediator of hyperammonemic neurotoxicity. The recent identification of a novel form of congenital hyperinsulinism associated with asymptomatic hyperammonemia assigns glutamate oxidation by glutamate dehydrogenase a more important role than previously recognized in β‐cell insulin secretion and hepatic and CNS ammonia detoxification. Disruptions of glutamate metabolism have been implicated in other clinical disorders, such as pyridoxine‐dependent seizures, confirming the importance of intact glutamate metabolism. This article will review glutamate metabolism and clinical disorders associated with disrupted glutamate metabolism. MRDD Research Reviews 2001;7:287–295. © 2001 Wiley‐Liss, Inc.