Phenylpyruvic acid may be a direct precursor of mandelic acid without intermediate transamination of phenylalanine

Biochem Pharmacol. 1993 Dec 3;46(11):2109-10. doi: 10.1016/0006-2952(93)90656-h.

Abstract

A series of compounds related to phenylalanine was administered to rats. Output of mandelic acid, a major but unexplained metabolite in phenylketonuria, was increased after the administration of phenylethanolamine or phenylpyruvic acid, whereas phenylethylamine or phenylalanine increased its excretion only marginally. Phenylacetic acid, previously suggested as a possible precursor in man, was almost without effect. It seems likely that mandelic acid can be formed from phenylpyruvic acid directly, without intermediate transamination to phenylalanine.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Female
  • Mandelic Acids / metabolism*
  • Mandelic Acids / urine
  • Phenethylamines / pharmacology
  • Phenylalanine / metabolism*
  • Phenylalanine / pharmacology
  • Phenylpyruvic Acids / metabolism*
  • Phenylpyruvic Acids / pharmacology
  • Rats
  • Rats, Wistar

Substances

  • Mandelic Acids
  • Phenethylamines
  • Phenylpyruvic Acids
  • Phenylalanine
  • mandelic acid
  • phenylpyruvic acid