Literature DB >> 1316525

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.

R J Wanders1, F A Wijburg, J Ruiter, J M Trijbels, W Ruitenbeek, R C Sengers, J A Bakkeren, N Feller.   

Abstract

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 cytochrome c oxidase, or other inhibitors of the mitochondrial respiratory chain. Amniocytes with an established cytochrome c oxidase deficiency were also investigated. Control amniocytes treated with azide as well as cytochrome c 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 cytochrome c oxidase deficiency and presumably of other systemic deficiencies of mitochondrial respiratory chain enzymes.

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Year:  1992        PMID: 1316525     DOI: 10.1007/bf01800349

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  13 in total

1.  A case of severe hypermetabolism of nonthyroid origin with a defect in the maintenance of mitochondrial respiratory control: a correlated clinical, biochemical, and morphological study.

Authors:  R LUFT; D IKKOS; G PALMIERI; L ERNSTER; B AFZELIUS
Journal:  J Clin Invest       Date:  1962-09       Impact factor: 14.808

2.  Detection of respiratory chain dysfunction by measuring lactate and pyruvate production in cultured fibroblasts.

Authors:  F A Wijburg; N Feller; W Ruitenbeek; J M Trijbels; R C Sengers; H R Scholte; H Przyrembel; R J Wanders
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

Review 3.  Disorders of the mitochondrial respiratory chain: clinical manifestations and diagnostic approach.

Authors:  J M Trijbels; R C Sengers; W Ruitenbeek; J C Fischer; J A Bakkeren; A J Janssen
Journal:  Eur J Pediatr       Date:  1988-11       Impact factor: 3.183

4.  Clinical presentation of mitochondrial respiratory chain defects in NADH-coenzyme Q reductase and cytochrome oxidase: clues to pathogenesis of Leigh disease.

Authors:  B H Robinson; L De Meirleir; M Glerum; G Sherwood; L Becker
Journal:  J Pediatr       Date:  1987-02       Impact factor: 4.406

5.  Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation.

Authors:  J M Shoffner; M T Lott; A M Lezza; P Seibel; S W Ballinger; D C Wallace
Journal:  Cell       Date:  1990-06-15       Impact factor: 41.582

Review 6.  Heteroplasmy in chronic external ophthalmoplegia: clinical and molecular observations.

Authors:  O Hurko; D R Johns; S L Rutledge; O C Stine; P L Peterson; N R Miller; M E Martens; D B Drachman; R H Brown; C P Lee
Journal:  Pediatr Res       Date:  1990-11       Impact factor: 3.756

7.  The use of skin fibroblast cultures in the detection of respiratory chain defects in patients with lacticacidemia.

Authors:  B H Robinson; D M Glerum; W Chow; R Petrova-Benedict; R Lightowlers; R Capaldi
Journal:  Pediatr Res       Date:  1990-11       Impact factor: 3.756

8.  Detection of "deleted" mitochondrial genomes in cytochrome-c oxidase-deficient muscle fibers of a patient with Kearns-Sayre syndrome.

Authors:  S Mita; B Schmidt; E A Schon; S DiMauro; E Bonilla
Journal:  Proc Natl Acad Sci U S A       Date:  1989-12       Impact factor: 11.205

9.  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.

Authors:  R J Wanders; C W van Roermund; M J van Wijland; R B Schutgens; J Heikoop; H van den Bosch; A W Schram; J M Tager
Journal:  J Clin Invest       Date:  1987-12       Impact factor: 14.808

10.  Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies.

Authors:  I J Holt; A E Harding; J A Morgan-Hughes
Journal:  Nature       Date:  1988-02-25       Impact factor: 49.962

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  4 in total

1.  Prenatal diagnosis of systemic disorders of the respiratory chain in cultured chorionic villus fibroblasts by study of ATP-synthesis in digitonin-permeabilized cells.

Authors:  R J Wanders; J P Ruiter; F A Wijburg; J Zeman; P Klement; J Houstek
Journal:  J Inherit Metab Dis       Date:  1996       Impact factor: 4.982

2.  Mitochondrial oxidative phosphorylation in digitonin-permeabilized chorionic villus fibroblasts: a new method with potential for prenatal diagnosis.

Authors:  R J Wanders; J P Ruiter; F A Wijburg
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982

Review 3.  Prerequisites and strategies for prenatal diagnosis of respiratory chain deficiency in chorionic villi.

Authors:  L Niers; L van den Heuvel; F Trijbels; R Sengers; J Smeitink
Journal:  J Inherit Metab Dis       Date:  2003       Impact factor: 4.982

4.  Lactic acidosis in long-chain fatty acid beta-oxidation disorders.

Authors:  F V Ventura; J P Ruiter; L IJlst; I T de Almeida; R J Wanders
Journal:  J Inherit Metab Dis       Date:  1998-08       Impact factor: 4.982

  4 in total

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