Literature DB >> 126826

Accumulation of 3-hydroxyisobutyric acid, 2-methyl-3-hydroxybutyric acid and 3-hydroxyisovaleric acid in ketoacidosis.

S Landaas.   

Abstract

1. Urine and serum samples from patients with ketoacidosis of varying degree and etiology have been examined by gas chromatography and mass spectrometry. 2. In addition to 3-hydroxyisovaleric acid, relatively high concentrations of two analogous hydroxy acids, 3-hydroxyisobutyric acid and 2-methyl-3-hydroxybutyric acid, were found in the urine. 3. There were highly significant positive correlations between the excreted amounts of the three acids. 4. Experiments on rats with isotope-labelled compounds revealed that the acids were formed by the degradation of leucine, isoleucine and valine. 5. The accumulation of the hydroxy acids during ketoacidosis is probably caused by a similar derangement of the metabolism of all three branched-chain amino acids.

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Year:  1975        PMID: 126826     DOI: 10.1016/0009-8981(75)90196-5

Source DB:  PubMed          Journal:  Clin Chim Acta        ISSN: 0009-8981            Impact factor:   3.786


  16 in total

1.  Conjugated linoleic acid isomers modulate protein expression profile in rat hepatocytes.

Authors:  E Rossi; L Della Casa; S Piana; A Iannone
Journal:  Genes Nutr       Date:  2012-05-05       Impact factor: 5.523

2.  Interorgan metabolism of valine.

Authors:  M E Brosnan; J Letto
Journal:  Amino Acids       Date:  1991-02       Impact factor: 3.520

3.  Amino acid catabolism by perfused rat hindquarter. The metabolic fates of valine.

Authors:  S H Lee; E J Davis
Journal:  Biochem J       Date:  1986-02-01       Impact factor: 3.857

4.  Beta-ketothiolase deficiency in a family confirmed by in vitro enzymatic assays in fibroblasts.

Authors:  R B Schutgens; B Middleton; J F vd Blij; J W Oorthuys; H A Veder; T Vulsma; W H Tegelaers
Journal:  Eur J Pediatr       Date:  1982-09       Impact factor: 3.183

5.  Biochemical and structural studies of uncharacterized protein PA0743 from Pseudomonas aeruginosa revealed NAD+-dependent L-serine dehydrogenase.

Authors:  Anatoli Tchigvintsev; Alexander Singer; Greg Brown; Robert Flick; Elena Evdokimova; Kemin Tan; Claudio F Gonzalez; Alexei Savchenko; Alexander F Yakunin
Journal:  J Biol Chem       Date:  2011-11-28       Impact factor: 5.157

6.  Deranged isoleucine metabolism during ketotic attacks in patients with methylmalonic acidaemia.

Authors:  M Duran; L Bruinvis; D Ketting; S K Wadman
Journal:  J Inherit Metab Dis       Date:  1978       Impact factor: 4.982

7.  Propionyl-CoA carboxylase deficiency with overflow of metabolites of isoleucine catabolism at all levels.

Authors:  H Przyrembel; H J Bremer; M Duran; L Bruinvis; D Ketting; S K Wadman; R Baumgartner; U Irle; C Bachmann
Journal:  Eur J Pediatr       Date:  1979-01-18       Impact factor: 3.183

8.  Biochemical studies in a patient with defects in the metabolism of acyl-CoA and sarcosine: another possible case of glutaric aciduria type II.

Authors:  N Gregersen; S Kølvraa; K Rasmussen; E Christensen; N J Brandt; F Ebbesen; F H Hansen
Journal:  J Inherit Metab Dis       Date:  1980       Impact factor: 4.982

9.  Urinary excretion of 2-methylacetoacetate, 2-methyl-3-hydroxybutyrate and tiglylglycine after isoleucine loading in the diagnosis of 2-methylacetoacetyl-CoA thiolase deficiency.

Authors:  S Aramaki; D Lehotay; L Sweetman; W L Nyhan; S C Winter; B Middleton
Journal:  J Inherit Metab Dis       Date:  1991       Impact factor: 4.982

10.  Valine metabolism. Gluconeogenesis from 3-hydroxyisobutyrate.

Authors:  J Letto; M E Brosnan; J T Brosnan
Journal:  Biochem J       Date:  1986-12-15       Impact factor: 3.857

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