Literature DB >> 8149631

The investigation of UDPGlucose and UDPGalactose concentration in red blood cells of patients with classical galactosaemia.

N J Keevill1, J B Holton, J T Allen.   

Abstract

UDPGlucose (UDPGlc) and UDPGalactose (UDPGal) are nucleotide sugars formed via the galactose metabolic pathway and are essential cofactors for the incorporation of galactose and glucose into complex glycoproteins and glycolipids. It has been proposed that in classical galactosaemia, where the enzyme galactose-1-phosphate uridyl transferase is deficient, the reaction product UDPGal is reduced leading to the long-term complications associated with the disease. We have measured the concentration of UDPGal and UDPGlc in red blood cells by high performance liquid chromatography (HPLC) in 16 children and 15 adult galactosaemics and compared the results with 30 and 27 control children and adults, respectively. The results indicate that UDPGal levels were found to be significantly reduced in galactosaemic patients and UDPGlc/UDPGal ratios significantly increased.

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Year:  1993        PMID: 8149631     DOI: 10.1016/0009-8981(93)90028-3

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


  7 in total

Review 1.  Galactosaemia: pathogenesis and treatment.

Authors:  J B Holton
Journal:  J Inherit Metab Dis       Date:  1996       Impact factor: 4.982

2.  UDP-glucose and UDP-galactose concentrations in cultured skin fibroblasts of patients with classical galactosaemia.

Authors:  N J Keevill; J B Holton; J T Allen
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982

Review 3.  Defective galactosylation in galactosemia: is low cell UDPgalactose an explanation?

Authors:  S Segal
Journal:  Eur J Pediatr       Date:  1995       Impact factor: 3.183

Review 4.  Galactosemia unsolved.

Authors:  S Segal
Journal:  Eur J Pediatr       Date:  1995       Impact factor: 3.183

Review 5.  Measurements of uridine diphosphate glucose and uridine diphosphate galactose--an appraisal.

Authors:  H N Kirkman
Journal:  Eur J Pediatr       Date:  1995       Impact factor: 3.183

Review 6.  Pathophysiology and targets for treatment in hereditary galactosemia: A systematic review of animal and cellular models.

Authors:  Minela Haskovic; Ana I Coelho; Jörgen Bierau; Jo M Vanoevelen; Laura K M Steinbusch; Luc J I Zimmermann; Eduardo Villamor-Martinez; Gerard T Berry; M Estela Rubio-Gozalbo
Journal:  J Inherit Metab Dis       Date:  2020-01-14       Impact factor: 4.982

7.  The 1-13 C galactose breath test in GALT deficient patients distinguishes NBS detected variant patients but does not predict outcome in classical phenotypes.

Authors:  Mendy M Welsink-Karssies; Dewi van Harskamp; Sacha Ferdinandusse; Carla E M Hollak; Hidde H Huidekoper; Mirian C H Janssen; E Marleen Kemper; Janneke G Langendonk; M Estela Rubio-Gozalbo; Maaike C de Vries; Frits A Wijburg; Henk Schierbeek; Annet M Bosch
Journal:  J Inherit Metab Dis       Date:  2020-01-22       Impact factor: 4.982

  7 in total

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