Literature DB >> 6682515

Skeletal muscle NAD+(P) and NADP+-dependent malic enzyme in Friedreich's ataxia.

E Bottacchi, S Di Donato.   

Abstract

Malic enzymes were studied in skeletal muscle from seven patients with Friedreich's ataxia (FA) and nine controls. Muscle contained three different malic enzymes. There were two strictly NADP+-dependent enzymes, one in the cytosol and one in mitochondria. These two enzymes are not allosteric. In FA muscle, activity of the mitochondrial NADP+-linked enzyme was significantly low and the cytosol NADP+-linked enzyme was significantly increased. A third malic enzyme, NAD+(P)-dependent, was found in the mitochondrial fraction. That enzyme had allosteric properties, and its activity was about the same in FA and control muscle.

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Year:  1983        PMID: 6682515     DOI: 10.1212/wnl.33.6.712

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  6 in total

1.  Mitochondrial malic enzyme in Friedreich's ataxia: failure to demonstrate reduced activity in cultured fibroblasts.

Authors:  R G Gray; D Kumar
Journal:  J Neurol Neurosurg Psychiatry       Date:  1985-01       Impact factor: 10.154

2.  Brainstem auditory-evoked responses and clinical picture in a one year follow-up of 18 patients with Friedreich ataxia.

Authors:  G Finocchiaro; A Formenti; F Baiocco; S Di Donato
Journal:  Ital J Neurol Sci       Date:  1985-03

3.  Functional genomic analysis of frataxin deficiency reveals tissue-specific alterations and identifies the PPARgamma pathway as a therapeutic target in Friedreich's ataxia.

Authors:  Giovanni Coppola; Daniele Marmolino; Daning Lu; Qing Wang; Miriam Cnop; Myriam Rai; Fabio Acquaviva; Sergio Cocozza; Massimo Pandolfo; Daniel H Geschwind
Journal:  Hum Mol Genet       Date:  2009-04-17       Impact factor: 6.150

4.  The clinical spectrum of Friedreich's ataxia in German families showing linkage to the FRDA locus on chromosome 9.

Authors:  W Müller-Felber; T Rossmanith; C Spes; S Chamberlain; D Pongratz; T Deufel
Journal:  Clin Investig       Date:  1993-02

5.  Mitochondrial enzymes in hereditary ataxias.

Authors:  K F Sheu; J P Blass; J M Cedarbaum; Y T Kim; B J Harding; J DeCicco
Journal:  Metab Brain Dis       Date:  1988-06       Impact factor: 3.584

6.  Myoadenylate deaminase deficiency in twins with recessive olivopontocerebellar atrophy.

Authors:  G Uziel; F Cornelio; C Gellera; C Perego; M Rimoldi; S DiDonato
Journal:  Ital J Neurol Sci       Date:  1986-02
  6 in total

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