Amino acid metabolism in liver disease

The impairment of transsulphuration during methionine degradation in hepatic failure can be counteracted by treatment with S-adenosylmethionine. Regarding the pathogenesis of hepatic encephalopathy, no convincing evidence exists for tryptophan, glutamine or glutamate being involved. Portal-systemic...

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Bibliographic Details
Main Authors: Holm, Eggert (Author) , Sedlaczek, Oliver (Author) , Grips, Eva (Author)
Format: Article (Journal)
Language:English
Published: 1999
In: Current opinion in clinical nutrition & metabolic care
Year: 1999, Volume: 2, Issue: 1, Pages: 47-53
ISSN:1473-6519
Online Access:Verlag, lizenzpflichtig, Volltext: https://journals.lww.com/co-clinicalnutrition/Fulltext/1999/01000/Amino_acid_metabolism_in_liver_disease.9.aspx
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Author Notes:Eggert Holm, Oliver Sedlaczek, Eva Grips
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Summary:The impairment of transsulphuration during methionine degradation in hepatic failure can be counteracted by treatment with S-adenosylmethionine. Regarding the pathogenesis of hepatic encephalopathy, no convincing evidence exists for tryptophan, glutamine or glutamate being involved. Portal-systemic shunting-induced hyperammonaemia may reduce plasma branched-chain amino acids. The glucose effect on urea synthesis does not exist in cirrhosis.
Item Description:Gesehen am 23.03.2022
Physical Description:Online Resource
ISSN:1473-6519