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Possible explanation for hyperglycinaemia in propionic acidaemia and methylmalonic acidaemia: Propionate and methylmalonate inhibit liver and brain mitochondrial glycine transport

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Journal of Inherited Metabolic Disease

Abstract

The effect of propionate and methylmalonate on the transport of glycine into rat liver and brain mitochondria was investigated. Both propionate and methylmalonate markedly inhibited mitochondrial glycine transport. These compounds also inhibited14CO2 production from [14C]glycine by isolated brain and liver mitochondria and glycine metabolism in rat brain cortex slices. These results are discussed with reference to hyperglycinaemia associated with propionic acidaemia and methylmalonic acidaemia and as a possible contributory factor to the pathological mechanisms in these conditions.

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References

  • Agrawal, H. C., Davis, J. M. and Himwich, W. A. Postnatal changes in free aminoacid pool of rat brain.J. Neurochem. 13 (1966) 607

    Article  PubMed  CAS  Google Scholar 

  • Ando, T., Nyhan, W. L., Conner, D., Rasmunssen, K., Donnell, G., Barnes, N., Cotton, D. and Hull, D. The oxidation of glycine and propionic acidemia with ketotic hyperglycinemia.Pediatr. Res. 6 (1972) 576

    Article  PubMed  CAS  Google Scholar 

  • Benavides, J., Garcia, M. L., López-Lahoya, J., Ugarte, M. and Valdivieso, F. Glycine transport in rat brain and liver mitochondria.Biochim. Biophys. Acta (1980). In press

  • Clark, J. B. and Nicklas, W. J. The metabolism of rat brain mitochondria.J. Biol. Chem. 245 (1970) 4724

    PubMed  CAS  Google Scholar 

  • De Groot, C. J., Everst, R. S., Gramsbergen, A. and Hommes, F. A. A study on the pathogenesis of non-ketotic hyperglycinemia. In Hommes, F. A. (ed.)Models for the Study of Inborn Errors of Metabolism. Elsevier North-Holland Biochemical Press, Amsterdam, 1979, pp. 183–190

    Google Scholar 

  • Hsia, Y. E., Scully, K. J. and Rosenberg, L. E. Defective propionate carboxylation in ketotic hyperglycinemia.Lancet 1 (1969) 757

    Article  PubMed  CAS  Google Scholar 

  • Hsia, Y. E., Scully, K. J. and Rosenberg, L. E. Inherited propionyl-CoA carboxylase deficiency in ketotic hyperglycinemia.J. Clin. Invest. 50 (1971) 121

    Article  Google Scholar 

  • Krebs, H. A. and Henseleit, H. Z. Intersuchungen uber die Harnstoffbilding in Tierkoper.Z. Physiol. Chem. 210 (1932) 33

    CAS  Google Scholar 

  • Lowry, O. H., Rosebrough, N. J., Farr, A. L. and Randall, R. J. Protein measurement with the Folin phenol reagent.J. Biol. Chem. 193 (1951) 265

    PubMed  CAS  Google Scholar 

  • Millar, K. R. and Lorentz, P. P. A gas chromatography method for the determination of methylmalonic acid in urine.J. Chromatogr. 101 (1974) 177

    Article  PubMed  CAS  Google Scholar 

  • O'Brien, W. E. Inhibition of glycine synthase by branched-chain α-ketoacids. A possible mechanism for abnormal glycine metabolism in ketotic hyperglycinemia.Arch. Biochem. Biophys. 189 (1978) 291

    Article  PubMed  Google Scholar 

  • Perry, T. L., Hansen, S., Diamond, S., Bullis, B., Mok, C. and Melançon, B. Volatile fatty acids in normal human physiological fluids.Clin. Chim. Acta 29 (1970) 369

    Article  PubMed  CAS  Google Scholar 

  • Resch, K., Imm, W., Ferber, E., Wallach, D. F. H. and Fischer, H. Quantitative determination of soluble and membrane proteins through their native fluorescence.Naturwissenschaften 58 (1971) 220

    Article  PubMed  CAS  Google Scholar 

  • Schneider, W. C. Intracellular distribution of enzymes. III. The oxidation of octanoic acid by rat liver fractions.J. Biol. Chem. 176 (1948) 259

    PubMed  CAS  Google Scholar 

  • Tanaka, K. Disorders of organic acids metabolism. In Gaulls, G. F. (ed.)Biology of Brain Disfunction. Plenum Press, New York, 1975, Vol. 3, pp. 145–214

    Google Scholar 

  • Walsh, J. M. and Clark, J. B. Studies on the control of 4-aminobutyrate metabolism in ‘synaptosomal’ and free rat brain mitochondria.Biochem. J. 160 (1976) 147

    PubMed  CAS  Google Scholar 

  • Winkler, H. H., Bygrave, F. L. and Lehninger, A. L. Characterization of the atractyloside-sensitive adenine nucleotide transport system in rat liver mitochondria.J. Biol. Chem. 243 (1968) 20

    PubMed  CAS  Google Scholar 

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Ugarte, M., Lopez-Lahoya, J., Garcia, M.L. et al. Possible explanation for hyperglycinaemia in propionic acidaemia and methylmalonic acidaemia: Propionate and methylmalonate inhibit liver and brain mitochondrial glycine transport. J Inherit Metab Dis 2, 93–96 (1979). https://doi.org/10.1007/BF01805665

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  • DOI: https://doi.org/10.1007/BF01805665

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