Literature DB >> 7366127

[Excretion of transamination products in hyperphenylalaninemia (author's transl)].

K Olek, P Wardenbach, D Byrd.   

Abstract

A low-phenylalanine diet was given for a period of three weeks to four untreated adult phenylketonurics with mental deficiency. One week before the diet was started, in the course of the diet and one week after its termination, some transamination products of phenylalanine, tryptophan and histidine were determined quantitatively. Each of the transamination products showed a positive correlation to the serum phenylalanine levels of the patients, probably due to the large affinity of 4-hydroxyphenylpyruvic acid and phenylpyruvic acid for the amino groups of the aromatic amino acids. This may also explain the low levels of epinephrine, norepinephrine and serotonine which has been observed by other authors in untreated phenylketonurics. Accordingly, treated phenylketonurics should suffer from a chronic deficiency of biogenic amines after termination of the low-phenylalanine diet.

Entities:  

Mesh:

Substances:

Year:  1980        PMID: 7366127     DOI: 10.1007/bf01477270

Source DB:  PubMed          Journal:  Klin Wochenschr        ISSN: 0023-2173


  17 in total

1.  Detection of some new abnormal metabolites in the urine of phenylketonuria.

Authors:  R J BOSCOTT; H BICKEL
Journal:  Scand J Clin Lab Invest       Date:  1953       Impact factor: 1.713

2.  Epinephrine metabolism in phenylketonuria.

Authors:  H L NADLER; D Y HSIA
Journal:  Proc Soc Exp Biol Med       Date:  1961 Aug-Sep

3.  Quantitative studies on the urinary excretion of unconjugated aromatic acids in phenylketonuria.

Authors:  R A Chalmers; R W Watts
Journal:  Clin Chim Acta       Date:  1974-09-30       Impact factor: 3.786

4.  The analysis of indolic tryptophan metabolites in human urine. Thin-layer chromatography and in situ quantitation.

Authors:  D J Byrd; W Kochen; D Idzko; E Knorr
Journal:  J Chromatogr       Date:  1974-07-17

5.  Transaminations between amino acids and keto acids elevated in phenylketonuria and maple syrup urine disease.

Authors:  G J Lees; N Weiner
Journal:  J Neurochem       Date:  1973-02       Impact factor: 5.372

6.  Substrate specificity of p-hydroxyphenylpyruvate hydroxylase.

Authors:  J H Fellman; T S Fujita; E S Roth
Journal:  Biochim Biophys Acta       Date:  1972-05-12

7.  Automatic column chromatographic analysis of urinary and serum imidazoles in patients with histidinaemia and normals.

Authors:  S K Wadman; P K De Bree; C Van der Heiden; F J Van Sprang
Journal:  Clin Chim Acta       Date:  1971-01       Impact factor: 3.786

8.  Enzymic studies on the biosynthesis of serotonin in mammalian brain.

Authors:  A Ichiyama; S Nakamura; Y Nishizuka; O Hayaishi
Journal:  J Biol Chem       Date:  1970-04-10       Impact factor: 5.157

9.  [Influence of storing conditions on the amino acid concentration in human serum (author's transl)].

Authors:  K Olek; S Uhlhaas; P Wardenbach; M Yamaguchi
Journal:  J Clin Chem Clin Biochem       Date:  1979-09

10.  Effect of stopping low-phenylalanine diet on intellectual progress of children with phenylketonuria.

Authors:  I Smith; M E Lobascher; J E Stevenson; O H Wolff; H Schmidt; S Grubel-Kaiser; H Bickel
Journal:  Br Med J       Date:  1978-09-09
View more
  2 in total

1.  A synopsis of the unconjugated acidic transamination metabolites of phenylalanine in phenylketonuria.

Authors:  U Langenbeck; A Behbehani; A Mench-Hoinowski
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

2.  Increased neurotransmitter biosynthesis in phenylketonuria induced by phenylalanine restriction or by supplementation of unrestricted diet with large amounts of tyrosine.

Authors:  C Lykkelund; J B Nielsen; H C Lou; V Rasmussen; A M Gerdes; E Christensen; F Güttler
Journal:  Eur J Pediatr       Date:  1988-12       Impact factor: 3.183

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.