Literature DB >> 6440113

Inherited lactic acidosis: correction of the defect in cultured fibroblasts.

P R Goodyer, G A Lancaster.   

Abstract

We report a case of familial lactic acidosis, lethal in the newborn period. Studies in intact fibroblasts identified a defect in the oxidative pathway of pyruvate metabolism. Although assay of pyruvate dehydrogenase on cell sonicates was not appreciably reduced, flux through the enzyme and other mitochondrial multienzyme dehydrogenases was severely impaired in intact cells. Deficient lactate conversion to carbon dioxide could be repaired by the addition to the incubation medium of electron acceptors such as methylene blue (25 micrograms/ml) or dichlorophenolindophenol (25 micrograms/ml).

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Year:  1984        PMID: 6440113     DOI: 10.1203/00006450-198411000-00018

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


  2 in total

1.  Deficiency of complex III of the mitochondrial respiratory chain in a patient with facioscapulohumeral disease.

Authors:  D M Slipetz; J R Aprille; P R Goodyer; R Rozen
Journal:  Am J Hum Genet       Date:  1991-03       Impact factor: 11.025

2.  Congenital deficiency of a 20-kDa subunit of mitochondrial complex I in fibroblasts.

Authors:  D M Slipetz; P R Goodyer; R Rozen
Journal:  Am J Hum Genet       Date:  1991-06       Impact factor: 11.025

  2 in total

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