Application of inhibitor titrations for the detection of oxidative phosphorylation defects in saponin-skinned muscle fibers of patients with mitochondrial diseases

被引:53
作者
Kuznetsov, AV
Winkler, K
Kirches, E
Lins, H
Feistner, H
Kunz, WS
机构
[1] UNIV MAGDEBURG,UNIV KLIN OTTO VON GUERICKE,NEUROL KLIN,D-39120 MAGDEBURG,GERMANY
[2] UNIV MAGDEBURG,UNIV KLIN OTTO VON GUERICKE,KLIN NEUROPHYSIOL,D-39120 MAGDEBURG,GERMANY
[3] UNIV MAGDEBURG,UNIV KLIN OTTO VON GUERICKE,INST NEUROPATHOL,D-39120 MAGDEBURG,GERMANY
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE | 1997年 / 1360卷 / 02期
关键词
mitochondrial disease; saponin-skinned muscle fiber; inhibitor titration; metabolic control analysis; flux control coefficient;
D O I
10.1016/S0925-4439(96)00072-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Inhibitor titrations were applied to characterize functional changes in mitochondrial energy metabolism in the skeletal muscle of patients with mitochondrial diseases. For this we titrated the maximal mitochondrial respiration rate of saponin-skinned muscle fibers isolated from the skeletal muscle biopsy with the specific inhibitors of mitochondrial oxidative phosphorylation complexes I, IV and V-rotenone, azide and oligomycin. For three patients with deletions of mitochondrial DNA and one patient with a complex I deficiency the titrations revealed at rather normal respiration activities of saponin-skinned fibers significant differences to healthy controls: (i) The inhibitor titration curves of the affected enzyme were much steeper and (ii) for almost complete inhibition of respiration a smaller amount of the inhibitor is necessary, The detailed analysis of the titration curves within the framework of metabolic control theory indicated elevated flux control coefficients of the respective complex of respiratory chain. On the other hand, for one patient with a mitochondrial DNA depletion syndrome, decreased respiration activities of skinned fibers but no redistribution of flux control was observed. We conclude, therefore, that application of inhibitor titrations and the quantitative description of the titration curve can be a valuable approach to elucidate functional defects of mitochondrial oxidative phosphorylation.
引用
收藏
页码:142 / 150
页数:9
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