Revisão Revisado por pares

Amino acid metabolism in liver disease

1999; Lippincott Williams & Wilkins; Volume: 2; Issue: 1 Linguagem: Inglês

10.1097/00075197-199901000-00009

ISSN

1473-6519

Autores

E. Holm, Oliver Sedlaczek, Eva Grips,

Tópico(s)

Alcoholism and Thiamine Deficiency

Resumo

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.

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