Effects of Cadmium and Mercury on the Upper Part of Skeletal Muscle Glycolysis in Mice

The effects of pre-incubation with mercury (Hg2+) and cadmium (Cd2+) on the activities of individual glycolytic enzymes, on the flux and on internal metabolite concentrations of the upper part of glycolysis were investigated in mouse muscle extracts. In the range of metal concentrations analysed we found that only hexokinase and phosphofructokinase, the enzymes that shared the control of the flux, were inhibited by Hg2+ and Cd2+. The concentrations of the internal metabolites glucose-6-phosphate and fructose-6-phosphate did not change significantly when Hg2+ and Cd2+ were added. A mathematical model was constructed to explore the mechanisms of inhibition of Hg2+ and Cd2+ on hexokinase and phosphofructokinase. Equations derived from detailed mechanistic models for each inhibition were fitted to the experimental data. In a concentration-dependent manner these equations describe the observed inhibition of enzyme activity. Under the conditions analysed, the integral model showed that the simultaneous inhibition of hexokinase and phosphofructokinase explains the observation that the concentrations of glucose-6-phosphate and fructose-6-phosphate did not change as the heavy metals decreased the glycolytic flux.

[1]  H. Passow,et al.  The general pharmacology of the heavy metals. , 1961, Pharmacological reviews.

[2]  Hans Ulrich Bergmeyer,et al.  Methods of Enzymatic Analysis , 2019 .

[3]  R. Schimke,et al.  Multiple hexokinases of rat tissues. Purification and comparison of soluble forms. , 1966, The Journal of biological chemistry.

[4]  B. Vallee,et al.  Biochemical effects of mercury, cadmium, and lead. , 1972, Annual review of biochemistry.

[5]  I. Brand,et al.  Rat liver phosphofructokinase. Purification and characterization of its reaction mechanism. , 1974, The Journal of biological chemistry.

[6]  Reinhart Heinrich,et al.  A linear steady-state treatment of enzymatic chains. General properties, control and effector strength. , 1974, European journal of biochemistry.

[7]  M. M. Bradford A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. , 1976, Analytical biochemistry.

[8]  Professor Dr. Ulrich Förstner,et al.  Metal Pollution in the Aquatic Environment , 1979, Springer Berlin Heidelberg.

[9]  Gunnar F. Nordberg,et al.  Handbook on the Toxicology of Metals , 1979 .

[10]  H. Westerhoff,et al.  Quantification of the contribution of various steps to the control of mitochondrial respiration. , 1982, The Journal of biological chemistry.

[11]  U. Behnke Methods of Enzymatic Analysis. Herausgegeben von H. U. Bergmeyer. Third Edition, Vol. III, Enzymes 1: Oxidoreductases, Transferases. 605 Seiten, zahlreiche Abb. und Tab. Verlag Chemie, Weinheim — Deerfield Beach, Florida—Basel 1983. Preis: 258,— DM , 1984 .

[12]  J. Schultz,et al.  Methods of Enzymatic Analysis, Vol. III: Enzymes 1: Oxidoreductases, Transferases, von H. U. Bergmeyer, 18 Abb., 43 Tab., XXVI, 605 S., Preis DM258,00, Verlag Chemie, Weinheim — Deerfield Beach/Florida — Basel 1983 , 1984 .

[13]  A. Hilmy,et al.  Bioaccumulation of cadmium: toxicity in Mugil cephalus. , 1985, Comparative biochemistry and physiology. C, Comparative pharmacology and toxicology.

[14]  A. Mas,et al.  Metales en sistemas biológicos , 1993 .

[15]  H. Kacser,et al.  A universal method for achieving increases in metabolite production. , 1993, European journal of biochemistry.

[16]  H. Kacser,et al.  Responses of metabolic systems to large changes in enzyme activities and effectors. 2. The linear treatment of branched pathways and metabolite concentrations. Assessment of the general non-linear case. , 1993, European journal of biochemistry.

[17]  H. Kacser,et al.  Responses of metabolic systems to large changes in enzyme activities and effectors. 1. The linear treatment of unbranched chains. , 1993, European journal of biochemistry.

[18]  M. Brand,et al.  Localisation of the sites of action of cadmium on oxidative phosphorylation in potato tuber mitochondria using top-down elasticity analysis. , 1994, European journal of biochemistry.

[19]  D A Fell,et al.  Physiological control of metabolic flux: the requirement for multisite modulation. , 1995, The Biochemical journal.

[20]  H. Kacser,et al.  The control of flux. , 1995, Biochemical Society transactions.

[21]  D. Fell Understanding the Control of Metabolism , 1996 .

[22]  M Cascante,et al.  Comparison of control analysis data using different approaches: modelling and experiments with muscle extract , 1997, FEBS letters.

[23]  D Quig,et al.  Cysteine metabolism and metal toxicity. , 1998, Alternative medicine review : a journal of clinical therapeutic.

[24]  M. Cascante,et al.  Application of metabolic control analysis to the study of toxic effects of copper in muscle glycolysis , 1999, FEBS letters.

[25]  M. Cascante,et al.  Combined enhancement of microtubule assembly and glucose metabolism in neuronal systems in vitro: decreased sensitivity to copper toxicity. , 1999, Biochemical and biophysical research communications.

[26]  M. Cascante,et al.  Organization-dependent effects of toxic bivalent ions microtubule assembly and glycolysis. , 2000, European journal of biochemistry.

[27]  Jack A. Taylor,et al.  Cadmium is a mutagen that acts by inhibiting mismatch repair , 2003, Nature Genetics.

[28]  D. Fell,et al.  Dynamic simulation of pollutant effects on the threonine pathway in Escherichia coli. , 2003, Comptes rendus biologies.

[29]  D. Morse,et al.  HEAVY METAL–INDUCED OXIDATIVE STRESS IN ALGAE 1 , 2003 .

[30]  Paula Aracena,et al.  Possible mechanisms underlying copper-induced damage in biological membranes leading to cellular toxicity. , 2005, Chemico-biological interactions.

[31]  A. Martín-González,et al.  Evaluation of heavy metal acute toxicity and bioaccumulation in soil ciliated protozoa. , 2006, Environment international.

[32]  R. Moreno-Sánchez,et al.  Determining and understanding the control of glycolysis in fast‐growth tumor cells , 2006, The FEBS journal.

[33]  Christopher J. Robinson,et al.  The effect of selected metals on the central metabolic pathways in biology: A review , 2007 .

[34]  Bonnie O. Leung,et al.  Cadmium(II) complex formation with cysteine and penicillamine. , 2009, Inorganic chemistry.

[35]  Torsten Schwede,et al.  The SWISS-MODEL Repository and associated resources , 2008, Nucleic Acids Res..

[36]  M. J. Wagner,et al.  Modular kinetic analysis reveals differences in Cd2+ and Cu2+ ion‐induced impairment of oxidative phosphorylation in liver , 2009, The FEBS journal.

[37]  Jean-Charles Portais,et al.  In silico strategy to rationally engineer metabolite production: A case study for threonine in Escherichia coli , 2009, Biotechnology and bioengineering.

[38]  Barbara M. Bakker,et al.  Measuring enzyme activities under standardized in vivo‐like conditions for systems biology , 2010, The FEBS journal.