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Mitochondrial enzymes related to glutamate and GABA metabolism in the hippocampus of young and aged rats: A quantitative histochemical study

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Abstract

Quantitative histochemistry (scanning microphotometry) was used to determine the activities of the mitochondrial enzymes NAD-linked isocitrate dehydrogenase (EC 1.1.1.41),l-glutamate dehydrogenase (EC 1.4.1.3) and GABA transaminase (EC 2.6.1.19) in various layers of the hippocampus (middle one third) of young (3–4 months old) and memory-impaired aged rats (28–30 months old). For comparison, determinations of cytochrome c oxidase (EC 1.9.3.1) as a marker for mitochondria and energy metabolism were also performed. The study showed that there was a layered reaction pattern in the hippocampus and that the cellular distribution and the levels of enzyme activity were different. However, the activities of the different enzymes (excepting GABA transaminase and cytochrome c oxidase) were significantly correlated in the hippocampus in both age groups. Age-dependent changes were only observed for NAD-linked isocitrate dehydrogenase and GABA transaminase (significant increases of activities in some layers of the hippocampus, preferentially in the terminal field of the perforant path). From the present study it is concluded that,1. the enzymatic complement of mitochondria in neurons and glia depends upon layer specific metabolic processes of the hippocampus (also with respect to glutamatergic and GABAergic terminal fields) indicating a layer specific interaction of the enzymes studied to produce or catabolize glutamate and GABA, and2. the age dependent changes of the studied enzymes are very restricted.

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References

  1. Ottersen, O. P., and Storm-Mathisen, J. 1989. Excitatory and inhibitory amino acids in the hippocampus. Pages 97–117,in Chan-Palay, V., and Köhler, C. (eds.), The Hippocampus—New Vistas, Neurol. Neurobiol. 52, Alan R. Liss, New York.

    Google Scholar 

  2. Hawkins, R. A., and Mans, A. M. 1983. Intermediary metabolism of carbohydrates and other fuels. Pages 259–294,in Lajtha, A. (ed.), Handbook of Neurochemistry, Plenum Press, New York.

    Google Scholar 

  3. Loverde, A. W., and Lehrer, G. M. 1973. Subcellular distribution of isocitrate dehydrogenases in neonatal and adult mouse brain. J. Neurochem. 20:441–448.

    PubMed  Google Scholar 

  4. Roberts, E. 1981. Strategies for identifying sources and sites of formation of GABA-precursor and transmitter glutamate in brain. Pages 91–102,in DiChiara, G., and Gessa, G. L. (eds.), Glutamate as a Neurotransmitter, Raven Press, New York.

    Google Scholar 

  5. Shank, R. P., and Campbell, G. M. 1982. Glutamine and alphaketoglutarate uptake and metabolism by nerve terminal enriched material from mouse cerebellum. Neurochem. Res. 7:601–616.

    PubMed  Google Scholar 

  6. Salganicoff, L., and Koeppe, R. E. 1968. Subcellular distribution of pyruvate carboxylase, diphosphopyridine nucleotide and triphosphopyridine nucleotide isocitrate dehydrogenases, and malate enzyme in rat brain. J. Biol. Chem. 243:3416–3420.

    PubMed  Google Scholar 

  7. Kugler, P. 1989. Localization of transmitter-metabolizing enzymes by enzyme histochemistry in the rat hippocampus. Pages 119–130,in Chan-Palay, V., and Köhler, C. (eds.), The Hippocampus—New Vistas, Neurol. Neurobiol. vol. 52, Alan R. Liss, New York.

    Google Scholar 

  8. McGeer, P. L., Eccles, J. C., and McGeer, E. G. 1987. Inhibitory amino acid neurotransmitters. Pages 197–234,in McGeer, P. L., Eccles, J. C., and McGeer, E. G. (eds.), Molecular Neurobiology of the Mammalian Brain, Plenum Press, New York.

    Google Scholar 

  9. Kugler, P. 1988. The enzyme histochemistry of neurotransmitter metabolism. Adv. Anat. Embryol. Cell Biol. 111:40–60.

    Google Scholar 

  10. Kugler, P. 1988. Quantitative enzyme histochemistry in the brain. Histochemistry 90:99–107.

    PubMed  Google Scholar 

  11. Kugler, P. 1990. Quantification of enzyme activities in brain sections by microphotometry. Int. J. Biochem. 23:657–661.

    Google Scholar 

  12. Kugler, P. 1990. Microphotometric determination of enzymes in brain sections. III. Glutamate dehydrogenase. Histochemistry 93:537–540.

    PubMed  Google Scholar 

  13. Kugler, P., and Baier, G. 1990. Microphotometric detemination of enzymes in brain sections. II. GABA transaminase. Histochemistry 93:501–505.

    PubMed  Google Scholar 

  14. Schuurman, T., Horvath, E., Spencer, D. G., and Traber, J. 1986. Old rats: an animal model for senile dementia. Pages 624–630,in Bes, A., Cahn, J., Cahn, R., and Hoyer, S. (eds.), Senile Dementias: Early Detections, John Libby Eurotext.

  15. Kugler, P., Vogel, S., Volk, H., and Schiebler, T. H. 1988. Cytochrome oxidase histochemistry in the rat hippocampus. A quantitative methodological study. Histochemistry 89:269–275.

    PubMed  Google Scholar 

  16. Butcher, R. G. 1978. The measurement in tissue sections of the two formazans derived from nitroblue tetrazolium in dehydrogenase reactions. Histochem. J. 10:739–744.

    PubMed  Google Scholar 

  17. Kugler, P., Vogel, S., and Gehm, M. 1988. Quantitative succinate dehydrogenase histochemistry in the hippocampus of aged rats. Histochemistry 88:299–307.

    PubMed  Google Scholar 

  18. Draper, N., and Smith, H. 1981. Applied Regression Analysis, John Wiley and Sons, New York. Chichester, Brisbane, Toronto.

    Google Scholar 

  19. Chee, P. Y., Dahl, J. L., and Fahien, L. A. 1979. The purification and properties of rat brain glutamate dehydrogenase. J. Neurochem. 33:53–60.

    PubMed  Google Scholar 

  20. Kretschmann, H. J., Tafesse, U., and Herrmann, A. 1982. Different volume changes of cerebral cortex and white matter during histological preparation. Microsc. Acta 86:13–24.

    PubMed  Google Scholar 

  21. Aoki, C., Milner, T. A., Sheu, K.-T. R., Blass, J. P., and Pickel, V. M. 1987. Regional distribution of astrocytes with intense immunoreactivity for glutamate dehydrogenase in rat brain: Implications for neuron-glia interactions in glutamate transmission. J. Neurosci. 7:2214–2231.

    PubMed  Google Scholar 

  22. Schousboe, A. 1981. Transport and metabolism of glutamate and GABA in neurons and glial cells. Int. Rev. Neurobiol. 22:1–45.

    PubMed  Google Scholar 

  23. Schousboe, A., Larsson, O. M., Drejer, J., Krogsgaard-Larsen, P., and Hertz, L. 1983. Uptake and release processes for glutamine, glutamate, and GABA in cultured neurons and astrocytes. Pages 297–315,in Hertz, L., Kvamme, E., McGeer, E., and Schousboe, A. (eds.), Glutamine, Glutamate, and GABA in the Central Nervous System, Alan R. Liss, New York.

    Google Scholar 

  24. Liu, C. J., Grandes, P., Matute, C., Cuenod, M., and Streit, P. 1989. Glutamate-like immunoreactivity revealed in rat olfactory bulb, hippocampus and cerebellum by monoclonal antibody and sensitive staining method. Histochemistry 90:427–445.

    PubMed  Google Scholar 

  25. Schmidbauer, J. M., Kugler, P., and Horvath, E. 1990. Glutamate producing aspartate aminotransferase in glutamatergic perforant path terminals of the rat hippocampus. Histochemistry 94:427–433.

    PubMed  Google Scholar 

  26. Norenberg, M. D., and Martinez-Hernandez, A. 1979. The structural localization of glutamine synthetase in astrocytes of rat brain. Brain Res. 161:303–310.

    PubMed  Google Scholar 

  27. Kugler, P., and Schiebler, T. H. 1989. Quantitative pharmaco-histochemical study on glutamate dehydrogenase in astrocytes of the rat hippocampus. Biomed. Res. 10, S.3:251–258.

    Google Scholar 

  28. Leong, S. F., and Clark, J. B. 1984. Regional development glutamate dehydrogenase in the rat brain. J. Neurochem. 43:106–111.

    PubMed  Google Scholar 

  29. Patel, A. J., Weir, M. D., Hunt, A., Takourdin, C. S. M., and Thomas, D. G. T. 1985. Distribution of glutamine synthetase and glial fibrillary acidic protein and correlation of glutamine synthetase with glutamate decarboxylase in different regions of the rat central nervous system. Brain Res. 331:1–9.

    PubMed  Google Scholar 

  30. Storm-Mathisen, J., and Fonnum, F. 1971. Quantitative histochemistry of glutamate decarboxylase in the rat hippocampal region. J. Neurochem. 18:1105–1111.

    PubMed  Google Scholar 

  31. Vitorica, J., Andres, A., Satrustegui, J., and Machado, A. 1981. Age-related quantitative changes in enzyme activities of rat brain. Neurochem. Res. 6:127–136.

    PubMed  Google Scholar 

  32. Ryder, E. 1980. Enzymatic profile of mitochondria isolated from selected brain regions of young adult and one year old rats. J. Franklin. Inst. 258:63–66.

    Google Scholar 

  33. Fonda, M. L., Acree, D. W., and Auerbach, S. B. 1973. The relationship of 4-aminobutyrate levels and its metabolism to age in brains of mice. Arch. Biochem. Biophys. 159:622–628.

    Google Scholar 

  34. Noda, Y., McGeer, P. L., and McGeer, E. G. 1982. Lipid peroxides in brain during aging and vitamin E deficiency: possible relations to changes in neurotransmitter indices. Neurobiol. Aging 3:173–178.

    PubMed  Google Scholar 

  35. Barnes, C. A. 1983. The physiology of the senescent hippocampus. Pages 87–108,in Seifert, W. (ed.), Neurobiology of the Hippocampus, Academic Press, London, New York.

    Google Scholar 

  36. Bondareff, W. 1979. Synaptic atrophy in the senescent hippocampus. Mech. Ageing Dev. 9:163–171.

    PubMed  Google Scholar 

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Kugler, P., Baier, G. Mitochondrial enzymes related to glutamate and GABA metabolism in the hippocampus of young and aged rats: A quantitative histochemical study. Neurochem Res 17, 179–185 (1992). https://doi.org/10.1007/BF00966797

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