On the renal tubular damage in hereditary tyrosinemia and on the formation of succinylacetoacetate and succinylacetone.

Abstract

Phenylalanine and homogentisate increase the concentration of succinylacetoacetate and succinylacetone both in serum and urine in patients with hereditary tyrosinemia and therefore increase the excretion of 5-aminolevulinate. Both phenylalanine and homogentisate cause a tubular proteinuria which is in agreement with our hypothesis that their metabolites maleylacetoacetate and fumarylacetoacetate are the toxic compounds in hereditary tyrosinemia. The patient with the highest excretion of succinylacetoacetate and succinylacetone has the slightest tubular proteinuria whereas the one with the lowest excretion of these compounds has the more pronounced tubular proteinuria. It is suggested that this is caused by a difference in the ability to reduce the presumed toxic compounds fumarylacetoacetate and maleylacetoacetate, i.e. the precursors of succinylacetoacetate.

• Authors: S P Fällström, B Lindblad, G Steen
• Journal: Acta paediatrica Scandinavica (Acta Paediatr Scand) Vol. 70 Issue 3 Pg. 315-20 ( 1981) ISSN: 0001-656X [Print] Sweden
• PMID: 7246125 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Acetoacetates
• Heptanoates
• Keto Acids
• Tyrosine
• Phenylalanine
• succinylacetone
• succinylacetoacetate
• Aminolevulinic Acid
• Homogentisic Acid

Topics

• Acetoacetates (biosynthesis)
• Amino Acid Metabolism, Inborn Errors (complications)
• Aminolevulinic Acid (urine)
• Child
• Heptanoates (biosynthesis)
• Homogentisic Acid
• Humans
• Infant
• Keto Acids (biosynthesis)
• Kidney Diseases (etiology)
• Kidney Tubules (pathology)
• Male
• Phenylalanine
• Proteinuria (etiology)
• Tyrosine (metabolism)