ISSN:
1573-7365
Keywords:
Ornithine transcarbamylase deficiency
;
congenital hyperammonemia
;
sparse-fur (spf) mouse
;
cerebral amino acids
;
seizures
Source:
Springer Online Journal Archives 1860-2000
Topics:
Medicine
Notes:
Abstract Congenital deficiencies of the urea cycle enzyme ornithine transcarbamylase (OTC) result in chronic hyperammonemia and severe neurological dysfunction including seizures and mental retardation. As part of a series of studies to elucidate the pathophysiologic mechanisms responsible for the CNS consequences of OTC deficiency, concentrations of ammonia-related and neurotransmitter amino acids were measured as their o-phthalaldehyde derivatives using high performance liquid chromatography with fluorescence detection in regions of the brains of sparse-fur (spf) mice, a mutant with an X-linked inherited defect of OTC. Compared to CD-1/Y controls, the brains of spf/Y mutant mice contained significant alterations of several amino acids. A generalized, up to 2-fold, increase of brain glutamine was observed, consistent with the exposure of these brains to increased concentrations of ammonia. Significant increases of brain alanine were also observed and, together with previous reports of increased concentrations of α-ketoglutarate, are consistent with ammonia-induced inhibition of α-ketoglutarate dehydrogenase in the brains of spf/Y mice. Increased brain content of the excitatory amino acid aspartate coul be responsible for the seizures frequently encountered in congenital OTC deficiency.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1007/BF01996073
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