Prenatal diagnosis of systemic disorders of the respiratory chain in cultured amniocytes and chorionic villus fibroblasts by studying the formation of lactate and pyruvate from glucose
- 4 March 1991
- journal article
- case report
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 15 (1) , 84-91
- https://doi.org/10.1007/bf01800349
Abstract
Summary: Formation of lactate and pyruvate from glucose was studied in cultured amniocytes and chorionic villus fibroblasts from controls, either untreated or treated with azide, an inhibitor of cytochromec oxidase, or other inhibitors of the mitochondrial respiratory chain. Amniocytes with an established cytochromec oxidase deficiency were also investigated.Control amniocytes treated with azide as well as cytochromec oxidase deficient amniocytes displayed strongly increased lactate‐to‐pyruvate ratios after incubation with glucose, compared to control cells. Elevated lactate‐to‐pyruvate ratios were also found in chorionic villus fibroblasts in which complexes I, III or IV were inhibited by rotenone, antimycin or azide, respectively. We conclude that measurement of lactate and pyruvate production from glucose in cultured amniocytes and/or chorionic villus fibroblasts allows adequate prenatal diagnosis of systemic cytochromec oxidase deficiency and presumably of other systemic deficiencies of mitochondrial respiratory chain enzymes.Keywords
This publication has 16 references indexed in Scilit:
- Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNALys mutationCell, 1990
- Detection of respiratory chain dysfunction by measuring lactate and pyruvate production in cultured fibroblastsJournal of Inherited Metabolic Disease, 1990
- Regulatory Complexity of Cytochrome c Oxidase and Its Defective Manifestation in Mitochondrial DiseasesPublished by Springer Nature ,1989
- Diagnostic Yield of the AutopsyNew England Journal of Medicine, 1988
- Prenatal Diagnosis of Cytochrome C Oxidase Deficiency by Biopsy of Chorionic VilliNew England Journal of Medicine, 1988
- Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathiesNature, 1988
- Peroxisomal fatty acid beta-oxidation in relation to the accumulation of very long chain fatty acids in cultured skin fibroblasts from patients with Zellweger syndrome and other peroxisomal disorders.Journal of Clinical Investigation, 1987
- Mitochondrial myopathiesJournal of Inherited Metabolic Disease, 1987
- Clinical presentation of mitochondrial respiratory chain defects in NADH-coenzyme Q reductase and cytochrome oxidase: Clues to pathogenesis of Leigh diseaseThe Journal of Pediatrics, 1987
- A CASE OF SEVERE HYPERMETABOLISM OF NONTHYROID ORIGIN WITH A DEFECT IN THE MAINTENANCE OF MITOCHONDRIAL RESPIRATORY CONTROL: A CORRELATED CLINICAL, BIOCHEMICAL, AND MORPHOLOGICAL STUDYJournal of Clinical Investigation, 1962