Literature DB >> 14640901

Polarographic evaluation of mitochondrial enzymes activity in isolated mitochondria and in permeabilized human muscle cells with inherited mitochondrial defects.

L Wenchich1, Z Drahota, T Honzík, H Hansíková, M Tesarová, J Zeman, J Houstek.   

Abstract

Inherited disturbances of the mitochondrial energy generating system represent a heterogeneous group of disorders associated with a broad spectrum of metabolic abnormalities and clinical symptoms. We used the polarographic and spectrophotometric method for detection of mitochondrial disorders, because these two techniques provide a different insight into mitochondrial function. In six patients suspected of mitochondrial disease we found defects of complex I (two patients), complex III (one patient), complex IV (two patients) and a combination of defect of complex III and IV (one patient). Citrate synthase activity, used as the reference enzyme, was not changed. A comparison of the two methods showed several differences in evaluation of mitochondrial enzymes activity due to the fact that both methods used different conditions for enzyme activity measurements. In contrast to oxygen consumption measurements, where the function of the whole-integrated respiratory chain is characterized, spectrophotometric measurements characterize activities of isolated complexes in disintegrated membranes. However, it may be concluded from our experiments that both methods provide useful and complementary data about mitochondrial energetic functions. Whereas spectrophotometric data are suitable for evaluation of maximal enzyme activities of mitochondrial enzyme complexes, polarographic data provide better information about enzyme activities in cells with mitochondrial defects under in situ conditions.

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Year:  2003        PMID: 14640901

Source DB:  PubMed          Journal:  Physiol Res        ISSN: 0862-8408            Impact factor:   1.881


  6 in total

1.  Substrate-specific changes in mitochondrial respiration in skeletal and cardiac muscle of hibernating thirteen-lined ground squirrels.

Authors:  Jason C L Brown; James F Staples
Journal:  J Comp Physiol B       Date:  2014-01-10       Impact factor: 2.200

Review 2.  The Biochemical Assessment of Mitochondrial Respiratory Chain Disorders.

Authors:  Nadia Turton; Neve Cufflin; Mollie Dewsbury; Olivia Fitzpatrick; Rahida Islam; Lowidka Linares Watler; Cara McPartland; Sophie Whitelaw; Caitlin Connor; Charlotte Morris; Jason Fang; Ollie Gartland; Liv Holt; Iain P Hargreaves
Journal:  Int J Mol Sci       Date:  2022-07-05       Impact factor: 6.208

3.  Whole Exome Sequencing Identifies the Genetic Basis of Late-Onset Leigh Syndrome in a Patient with MRI but Little Biochemical Evidence of a Mitochondrial Disorder.

Authors:  Michael Nafisinia; Yiran Guo; Xiao Dang; Jiankang Li; Yulan Chen; Jianguo Zhang; Nicole J Lake; Wendy A Gold; Lisa G Riley; David R Thorburn; Brendan Keating; Xun Xu; Hakon Hakonarson; John Christodoulou
Journal:  JIMD Rep       Date:  2016-06-26

Review 4.  The in-depth evaluation of suspected mitochondrial disease.

Authors:  Richard H Haas; Sumit Parikh; Marni J Falk; Russell P Saneto; Nicole I Wolf; Niklas Darin; Lee-Jun Wong; Bruce H Cohen; Robert K Naviaux
Journal:  Mol Genet Metab       Date:  2008-02-01       Impact factor: 4.797

5.  Measurement of mitochondrial oxygen consumption using a Clark electrode.

Authors:  Zhihong Li; Brett H Graham
Journal:  Methods Mol Biol       Date:  2012

6.  YME1L controls the accumulation of respiratory chain subunits and is required for apoptotic resistance, cristae morphogenesis, and cell proliferation.

Authors:  Lukas Stiburek; Jana Cesnekova; Olga Kostkova; Daniela Fornuskova; Kamila Vinsova; Laszlo Wenchich; Josef Houstek; Jiri Zeman
Journal:  Mol Biol Cell       Date:  2012-01-19       Impact factor: 4.138

  6 in total

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