Literature DB >> 12889660

Mitochondrial oxidative phosphorylation: pitfalls and tips in measuring and interpreting enzyme activities.

D Chretien1, P Rustin.   

Abstract

Mitochondrial oxidative phosphorylation (OXPHOS) is fundamental in all aspects of cellular life in aerobic cells and organisms. It is therefore not surprising that a variety of diseases have been attributed to dysfunction of the OXPHOS enzymes. Assessment of OXPHOS in human samples has proved to be a difficult task over years, even when relying on well-established methods. The complexity and the flexibility of the mitochondrial organization in cells account for a large part in the difficulties encountered in assessing OXPHOS activity. Nevertheless, a careful and detailed analysis of OXPHOS enzyme activity in cells or biopsy samples from patients at risk provides diagnosis of potential OXPHOS deficiency. Problems inherent in the use of human material, mostly the small size of the samples to be analysed, are difficult to resolve. However, cautious handling of these samples permits reasonable confidence to be reached in the interpretation of the data.

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Year:  2003        PMID: 12889660     DOI: 10.1023/a:1024437201166

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


  12 in total

1.  Mitochondria, from cell death to proliferation.

Authors:  Pierre Rustin
Journal:  Nat Genet       Date:  2002-04       Impact factor: 38.330

2.  Assessment of the mitochondrial respiratory chain.

Authors:  P Rustin; D Chretien; T Bourgeron; A Wucher; J M Saudubray; A Rotig; A Munnich
Journal:  Lancet       Date:  1991-07-06       Impact factor: 79.321

Review 3.  Morphological studies of skeletal muscle in lactic acidosis.

Authors:  N B Romero; A Lombès; G Touati; O Rigal; P Frachon; M A Cheval; M Giraud; S Possekel; M Fardeau; H Ogier de Baulny
Journal:  J Inherit Metab Dis       Date:  1996       Impact factor: 4.982

4.  Superoxide-induced massive apoptosis in cultured skin fibroblasts harboring the neurogenic ataxia retinitis pigmentosa (NARP) mutation in the ATPase-6 gene of the mitochondrial DNA.

Authors:  V Geromel; N Kadhom; I Cebalos-Picot; O Ouari; A Polidori; A Munnich; A Rötig; P Rustin
Journal:  Hum Mol Genet       Date:  2001-05-15       Impact factor: 6.150

Review 5.  Clinical spectrum and diagnosis of mitochondrial disorders.

Authors:  A Munnich; P Rustin
Journal:  Am J Med Genet       Date:  2001

Review 6.  Mitochondria, oxygen free radicals, and apoptosis.

Authors:  S Raha; B H Robinson
Journal:  Am J Med Genet       Date:  2001

7.  Fluxes of nicotinamide adenine dinucleotides through mitochondrial membranes in human cultured cells.

Authors:  P Rustin; B Parfait; D Chretien; T Bourgeron; F Djouadi; J Bastin; A Rötig; A Munnich
Journal:  J Biol Chem       Date:  1996-06-21       Impact factor: 5.157

8.  Biochemical parameters for the diagnosis of mitochondrial respiratory chain deficiency in humans, and their lack of age-related changes.

Authors:  D Chretien; J Gallego; A Barrientos; J Casademont; F Cardellach; A Munnich; A Rötig; P Rustin
Journal:  Biochem J       Date:  1998-01-15       Impact factor: 3.857

Review 9.  Coenzyme Q(10) and idebenone in the therapy of respiratory chain diseases: rationale and comparative benefits.

Authors:  Vanna Geromel; Niklas Darin; Dominique Chrétien; Paule Bénit; Pascale DeLonlay; Agnès Rötig; Arnold Munnich; Pierre Rustin
Journal:  Mol Genet Metab       Date:  2002 Sep-Oct       Impact factor: 4.797

Review 10.  Biochemical and molecular investigations in respiratory chain deficiencies.

Authors:  P Rustin; D Chretien; T Bourgeron; B Gérard; A Rötig; J M Saudubray; A Munnich
Journal:  Clin Chim Acta       Date:  1994-07       Impact factor: 3.786

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  9 in total

Review 1.  Xeroderma pigmentosum: overview of pharmacology and novel therapeutic strategies for neurological symptoms.

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Review 2.  Neurodevelopmental manifestations of mitochondrial disease.

Authors:  Marni J Falk
Journal:  J Dev Behav Pediatr       Date:  2010-09       Impact factor: 2.225

Review 3.  Mitochondrial disorders: clinical presentation and diagnostic dilemmas.

Authors:  J A M Smeitink
Journal:  J Inherit Metab Dis       Date:  2003       Impact factor: 4.982

Review 4.  Presentation and diagnosis of mitochondrial disorders in children.

Authors:  Mary Kay Koenig
Journal:  Pediatr Neurol       Date:  2008-05       Impact factor: 3.372

5.  Mitochondrial Oxygen Consumption by the Foreskin and its Fibroblast-rich Culture.

Authors:  Fatma Al-Jasmi; Thachillath Pramathan; Adnan Swid; Bahjat Sahari; Harvey S Penefsky; Abdul-Kader Souid
Journal:  Sultan Qaboos Univ Med J       Date:  2013-06-25

6.  Clinical variability in neurohepatic syndrome due to combined mitochondrial DNA depletion and Gaucher disease.

Authors:  Julie Harvengt; Catherine Wanty; Boel De Paepe; Christine Sempoux; Nicole Revencu; Joél Smet; Rudy Van Coster; Willy Lissens; Sara Seneca; Laurent Weekers; Etienne Sokal; François-Guillaume Debray
Journal:  Mol Genet Metab Rep       Date:  2014-05-10

7.  Hybrid gel electrophoresis using skin fibroblasts to aid in diagnosing mitochondrial disease.

Authors:  Christopher Newell; Aneal Khan; David Sinasac; John Shoffner; Marisa W Friederich; Johan L K Van Hove; Stacey Hume; Jane Shearer; Iveta Sosova
Journal:  Neurol Genet       Date:  2019-05-01

Review 8.  Analysis of Mitochondrial Function, Structure, and Intracellular Organization In Situ in Cardiomyocytes and Skeletal Muscles.

Authors:  Andrey V Kuznetsov; Sabzali Javadov; Raimund Margreiter; Judith Hagenbuchner; Michael J Ausserlechner
Journal:  Int J Mol Sci       Date:  2022-02-18       Impact factor: 5.923

9.  Subcomplex Ilambda specifically controls integrated mitochondrial functions in Caenorhabditis elegans.

Authors:  Marni J Falk; Julie R Rosenjack; Erzsebet Polyak; Wichit Suthammarak; Zhongxue Chen; Phil G Morgan; Margaret M Sedensky
Journal:  PLoS One       Date:  2009-08-12       Impact factor: 3.240

  9 in total

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