Journal of Inherited Metabolic Disease 2005-01-01

N-carbamylglutamate protects patients with decompensated propionic aciduria from hyperammonaemia.

B Gebhardt, S Dittrich, S Parbel, S Vlaho, O Matsika, H Bohles

文献索引：J. Inherit. Metab. Dis. 28(2) , 241-4, (2005)

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摘要

In patients with propionic aciduria, the accumulating metabolite propionyl-CoA causes a disturbance of the urea cycle via the inhibition of N-acetylglutamate synthesis. Lack of this allosteric activator results in an inhibition of carbamoylphosphate synthase (CPS). This finally leads to hyperammonaemia. In two patients with decompensated propionic aciduria the CPS activator carbamylglutamate was tested for its ability to antagonize the propionyl-CoA associated hyperammonaemia. Oral carbamyl glutamate administration resulted in a significant increase in ammonia detoxification and could avoid further dialysis therapy. Safe, fast and easy to administer, carbamyl glutamate improves the acute therapy of decompensated propionic aciduria by increasing ammonia detoxification and avoiding hyperammonaemia.