Application of metabolic control analysis to the study of toxic effects of copper in muscle glycolysis

被引:24
作者
Jannaschk, D
Burgos, M
Centelles, JJ
Ovadi, J
Cascante, M [1 ]
机构
[1] Univ Barcelona, Fac Chem, Dept Biochem & Mol Biol, C Marti Franques 1, Barcelona 08028, Spain
[2] ENSPG, INPG, Mat & Genie Phys Lab, F-38402 St Martin Dheres, France
[3] Hungarian Acad Sci, Inst Enzymol, Biol Res Ctr, H-1518 Budapest, Hungary
关键词
glycolysis; copper; inhibition; metabolic control analysis;
D O I
10.1016/S0014-5793(99)00117-9
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
Experimental and model studies have been performed to characterise the effects of Cu2+ on the activities of individual glycolytic enzymes and on the flux and internal metabolite concentrations of the upper part of glycolysis in mouse muscle extracts. Cu2+ significantly inhibited the triosephosphate production from glucose with an IC50 of about 6.0 mu M. At a similar extension Cu2+ inhibited hexokinase and phosphofructokinase, with an IC50 of 6.2 mu M and 6.4 mu M respectively, whereas the effects on the activities of aldolase, phosphoglucose isomerase and the internal metabolite levels were not significant, Flux control coefficients and flux response coefficients were determined in the presence of copper concentrations between 0 and 10 mu M. The same values of flux control coefficients for hexokinase and for phosphofructokinase (0.8 and 0.2 respectively) were found in absence and in presence of copper. At Cu2+ equal to the flux IC50, the response coefficient was -1. The elasticity coefficients for hexokinase and phosphofructokinase at Cu2+ equal to the IC50 were also -1, A mathematical model was used to analyze the effect of copper on glycolysis under different conditions using experimental kinetic parameters and rate equations for enzymatic reactions of the upper part of glycolysis. (C) 1999 Federation of European Biochemical Societies.
引用
收藏
页码:144 / 148
页数:5
相关论文
共 22 条
[1]  
AHAMMADSAHIB K I, 1987, Journal of Biochemical Toxicology, V2, P169, DOI 10.1002/jbt.2570020303
[2]  
Bergmeyer HU, 1984, METHODS ENZYMATIC AN, VIII
[3]  
Bergmeyer HU, 1984, METHODS ENZYMATIC AN, VII
[4]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[5]  
BRAND IA, 1974, J BIOL CHEM, V249, P7824
[6]   USE OF IMPLICIT METHODS FROM GENERAL SENSITIVITY THEORY TO DEVELOP A SYSTEMATIC-APPROACH TO METABOLIC CONTROL .1. UNBRANCHED PATHWAYS [J].
CASCANTE, M ;
FRANCO, R ;
CANELA, EI .
MATHEMATICAL BIOSCIENCES, 1989, 94 (02) :271-288
[7]  
EHLDE M, 1995, COMPUT APPL BIOSCI, V11, P201
[8]   CONTAMINATION OF ENVIRONMENT WITH HEAVY-METALS EMITTED FROM AUTOMOTIVES [J].
FALAHIARDAKANI, A .
ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY, 1984, 8 (02) :152-161
[9]  
Fell D., 1997, Understanding the control of metabolism
[10]  
GROSSBARD L, 1966, J BIOL CHEM, V241, P3546