Literature DB >> 3080729

Metabolism of branched-chain amino acids in fibroblasts from patients with maple syrup urine disease and other abnormalities of branched-chain ketoacid dehydrogenase activity.

I Yoshida, L Sweetman, W L Nyhan.   

Abstract

The metabolism of branched-chain amino acids was studied in cultured fibroblasts from patients with branched-chain ketoacid dehydrogenase deficiency using 1-14C- and UL-14C-leucine and valine. The formation of 14CO2 from 1-14C-valine or 1-14C-leucine was 1-3% of normal. In fibroblasts of patients with associated lactic acidemia the values were 4-29% of control. Analysis of organic acid products revealed that in both patients and controls the amount of labeled alpha-ketoisovalerate recovered after incubation with 1-14C-valine was one-third of the amount of alpha-ketoisocaproate recovered after incubation with 1-14C-leucine. Very little alpha-hydroxyisocaproate was produced, while the amount of alpha-hydroxyisovalerate was about 10% of the alpha-ketoisovalerate. Unexpectedly beta-hydroxyisobutyrate was found to be the major metabolic product of UL-14C-valine in normal fibroblasts. Large accumulations of beta-hydroxyisovalerate were found in normal fibroblasts using UL-14C-leucine. There were little or no conversions to these compounds in fibroblasts of patients with branched-chain ketoacid dehydrogenase deficiency. There were substantial conversions in the patients in whom dehydrogenase deficiency was associated with lactic acidemia.

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Year:  1986        PMID: 3080729     DOI: 10.1203/00006450-198602000-00016

Source DB:  PubMed          Journal:  Pediatr Res        ISSN: 0031-3998            Impact factor:   3.756


  2 in total

1.  Biallelic Mutations in LIPT2 Cause a Mitochondrial Lipoylation Defect Associated with Severe Neonatal Encephalopathy.

Authors:  Florence Habarou; Yamina Hamel; Tobias B Haack; René G Feichtinger; Elise Lebigot; Iris Marquardt; Kanetee Busiah; Cécile Laroche; Marine Madrange; Coraline Grisel; Clément Pontoizeau; Monika Eisermann; Audrey Boutron; Dominique Chrétien; Bernadette Chadefaux-Vekemans; Robert Barouki; Christine Bole-Feysot; Patrick Nitschke; Nicolas Goudin; Nathalie Boddaert; Ivan Nemazanyy; Agnès Delahodde; Stefan Kölker; Richard J Rodenburg; G Christoph Korenke; Thomas Meitinger; Tim M Strom; Holger Prokisch; Agnes Rotig; Chris Ottolenghi; Johannes A Mayr; Pascale de Lonlay
Journal:  Am J Hum Genet       Date:  2017-07-27       Impact factor: 11.025

2.  Mutations in human lipoyltransferase gene LIPT1 cause a Leigh disease with secondary deficiency for pyruvate and alpha-ketoglutarate dehydrogenase.

Authors:  Yohan Soreze; Audrey Boutron; Florence Habarou; Christine Barnerias; Luc Nonnenmacher; Hélène Delpech; Asmaa Mamoune; Dominique Chrétien; Laurence Hubert; Christine Bole-Feysot; Patrick Nitschke; Isabelle Correia; Claude Sardet; Nathalie Boddaert; Yamina Hamel; Agnès Delahodde; Chris Ottolenghi; Pascale de Lonlay
Journal:  Orphanet J Rare Dis       Date:  2013-12-17       Impact factor: 4.123

  2 in total

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