Skip to main content
Log in

Interactions between valproate, glutamate, aspartate, and GABA with respect to uptake in astroglial primary cultures

  • Original Articles
  • Published:
Neurochemical Research Aims and scope Submit manuscript

Abstract

Astrocytes have been proposed to regulate the extracellular space in the brain, even if rather little is known about their specific functions. One possibility for obtaining more knowledge on the functions of astroglial cells is to examine how they respond on exposure to pharmacological agents. Na+-valproate is an anticonvulsive drug which is used in the treatment of several types of epilepsy. The mechanisms of action of the drug are not fully understood, but the GABA-ergic system, both in neurons and astrocytes, has been shown to be affected. In the present study, the effects of valproate were investigated on astroglial cells in primary cultures from newborn rat cerebral cortex. The transport of the drug itself and its effects on the transport of the amino acid transmitters glutamate, aspartate and γ-aminobutyric acid (GABA) into astrocytes were examined. The [3H]valproate transport into the astrocytes was increased after exposure tol-glutamate but notl-aspartate. On the other hand, after acute exposure for the drug, the transport of [3H]l-glutamate and [3H]l-aspartate decreased, as also did the affinity but not the transport capacity for the [3H]GABA uptake. However, after 5 days chronic valproate exposure, no effects could be seen on the uptake kinetics ofl-glutamate orl-aspartate. For GABA, the affinity decreased, while the transport capacity remained unchanged compared with controls. The results showed that valproate, glutamate, aspartate and GABA were capable of interacting significantly with each others transport into the astrocytes.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Hartz, L., and Schousboe, A. 1980. Interactions between neurons and astrocytes in the turnover of GABA and glutamate. GABA neurotransmission. Brain Res. Bull. 52:389–395.

    Google Scholar 

  2. Drejer, I., Larsson, O. M., and Schoushoe, A. 1983. Characterization of uptake and release processes for D- and L-aspartate in primary cultures of astrocytes and cerebellar granule cells. Neurochem. Res. 8:231–243.

    PubMed  Google Scholar 

  3. Hansson, E., Eriksson, P., and Nilsson, M. 1985. Amino acid and monoamine transport in primary astroglial cultures from defined brain regions. Neurochem. Res. 10:1335–1341.

    Google Scholar 

  4. Murphy, S., and Pearce, B. 1987. Functional receptors for neurotransmitter on astroglial cells. Neurosci. 22:381–394.

    Google Scholar 

  5. Hansson, E. 1988. Astroglia from defined brain regions as studied with primary cultures. Progr. Neurobiol. 30:369–397.

    PubMed  Google Scholar 

  6. Kimelberg, H. K. (ed.) 1988. Glial Cell Receptors. Raven Press, New York.

    Google Scholar 

  7. Walz, W., and Hertz, L. 1983. Comparison between fluxes of potassium and of chloride in astrocytes in primary cultures. Brain Res. 277:321–328.

    PubMed  Google Scholar 

  8. Walz, W., and Kimelberg, H. K. 1985. Differences in cation transport properties of primary astrocyte cultures from mouse and rat brain. Brain Res. 340:333–340.

    PubMed  Google Scholar 

  9. Usowicz, M. M., Gallo, V., and Cull-Candy, S. G. 1989. Multiple conductance channels in type-2 cerebellar astrocytes activated by excitatory amino acids. Nature 339:380–383.

    PubMed  Google Scholar 

  10. Barres, B. A., Chun, L. L. Y., and Corey, D. P. 1990. Ion channels in vertebrate glia. Annu. Rev. Neurosci. 13:441–474.

    PubMed  Google Scholar 

  11. Grisar, T. 1986. Neuron-glia relationships in human and experimental epilepsy: A biochemical point of view. Pages 1045–1073. in A. V. Delgado-Escueta, A. A. Ward, Jr., D. M. Woodbury, and R. J. Porter (eds.) Adv. Neurol. Vol. 44, Raven Press, New York.

    Google Scholar 

  12. Barron, K. D., Dentinger, M. P., Kimelberg, H. K., Nelson, L. R., Bourke, R. S., Keegan, S., Mankes, R., and Cragoe, E. J. Jr. 1988. Ultrastructural features of brain injury model in cat I. Vascular and neuroglial changes and the prevention of astroglial swelling by fluorenyl (aryloxy) alkanoic acid derivate (L644, 711). Acta Neuropathol. 75:295–307.

    PubMed  Google Scholar 

  13. Whtie, H. S., Yen-Chow, Y. C., Chow, S. Y., Kemp, I. W., and Woodbury, D. M. 1985. Effects of phenytoin on primary glial cell cultures. Epilepsia 26:58–68.

    PubMed  Google Scholar 

  14. Krogsgaard-Larsen, P., Falck, E., Larsson, O. M., and Schousboe, A. 1987. GABA uptake inhibitors: relevance to antiepileptic drug research. Epilepsy Res. 1:77–93.

    PubMed  Google Scholar 

  15. Fonnum, F. 1984. Glutamate: A neurotransmitter in mammalian brain. J. Neurochem. 42:1–11.

    PubMed  Google Scholar 

  16. Roberts, E. 1984. GABA related phenomena, models of nervous system function and seizures. Ann. Neurol. 16(Suppl.):77–89.

    Google Scholar 

  17. Larsson, O. M., Falck, E., Krogsgaard-Larsen, P., and Schousboe, A. 1988. Kinetic characterization of inhibition of γ-aminobutyric acid uptake into cultured neurons and astrocytes by 4.4-diphenyl-3-butenyl derivatives of nipecotic acid and guvacine. J. Neurochem. 50:818–823.

    PubMed  Google Scholar 

  18. Jawad, S., Yuen, W. C., Peck, A. W., Hamilton, J. J., Oxley, I.-R., and Richéns, A. 1987. Lamotrigine: single dose pharmacokinetics and initial 1 week experience in refractory epilepsy. Epilepsy Res. 1:202–208.

    PubMed  Google Scholar 

  19. Gram, L. 1988. Experimental studies and controlled clinical testing of valproate and vigabatrin. Acta Neurol. Scand. 78:241–270.

    PubMed  Google Scholar 

  20. Nilsson, M., Hansson, E., and Rönnbäck, L. 1990. Transport of Na+-valproate and its effects on GABA uptake in astroglial primary culture. Neurochem. Res. 15:769–773.

    PubMed  Google Scholar 

  21. Hansson, E., Rönnbäck, L., Persson, L. I., Lowenthal, A., Noppe, M., Alling, C., and Karlsson, B. 1984. Cellular composition of primary cultures from cerebral cortex, striatum, hippocampus, brain stem and cerebellum. Brain Res. 300:9–18.

    PubMed  Google Scholar 

  22. Lowry, O. H., Rosebrough, N. I., Farr, A. L., and Randall, R. I. 1951. Protein measurement with the Folin phenol reagent. J. Biol. Chem. 193:265–275.

    PubMed  Google Scholar 

  23. Balcar, V. J., and Mandel, P. 1976. Inhibition of high affinity uptake of GABA by branched fatty acids. Experientia 32:904–905.

    PubMed  Google Scholar 

  24. Löscher, W. 1980. Effect of inhibitors of GABA transaminase on the synthesis, binding, uptake and metabolism of GABA. J. Neurochem. 34:1603–1608.

    PubMed  Google Scholar 

  25. Ross, S. M., and Craig, C. R. 1981. Studies on gamma-amino butyric acid transport in cobalt experimental epilepsy in the rat. J. Neurochem. 36:1006–1011.

    PubMed  Google Scholar 

  26. Hydén, H., Cupello, A., and Palm, A. 1984. Inhibition by sodium valproate of the transport of GABA through the Deiters' neuron plasma membrane. Neuropharmacology 23:319–321.

    PubMed  Google Scholar 

  27. Klee, M. R., Akaike, N., Oomura, Y., and Manuyama, T. 1985. Valproate reduces Na+ dependent GABA uptake. Pflügers Arch. Eur. J. Physiol. 405:R7.

    Google Scholar 

  28. Phelan, P., Regan, C., Killty, C., and Dunne, A., 1985. Sodium valproate stimulates the particulate form of glutamine synthetase in rat brain. Neuropharmacology 24:895–902.

    PubMed  Google Scholar 

  29. Larsson, O. M., Gram, L., Schousboe, I., and Schousboe, A. 1986. Differential effect of gamma-vinyl GABA and valproate on GABA-transaminase from cultures neurons and astrocytes. Neuropharmacology 25:617–625.

    PubMed  Google Scholar 

  30. Preisendörfer, U., Zeise, M. L., and Klee, R. 1987. Valproate enhances inhibitory postsynaptic potentials in hippocampal neurons in vitro. Brain Res. 435:213–219.

    PubMed  Google Scholar 

  31. Cotariu, D., Zaidman, J. L., and Evans, S. 1990. Neurophysiological changes evoked by valproic acid in the central nervous system. Progr.Neurobiol. 34:343–354.

    PubMed  Google Scholar 

  32. Stelzer, A., and Wong, K. S. 1989. GABAa responses in hippocampal neurons are potentiated by glutamate. Nature. 337:170–173.

    PubMed  Google Scholar 

  33. Perlmann, B. J., and Goldstein, D. B. 1984. Membrane-disordering potency and anticonvulsant action of valproic acid and other short-chain fatty acids. Mol. Pharmacol. 26:83–89.

    PubMed  Google Scholar 

  34. Hansson, E., and Rönnbäck, L. 1989. Regulation of glutamate and GABA transport by adrenoceptors in primary astroglial cell cultures. Life Sci. 44:27–34.

    PubMed  Google Scholar 

  35. Hansson, E., and Rönnbäck, L. 1991. Receptor regulation of the glutamate, GABA and taurine high affinity uptake into the astrocytes in primary culture. Brain Res. 548:215–221.

    PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Nilsson, M., Hansson, E. & Rönnbäck, L. Interactions between valproate, glutamate, aspartate, and GABA with respect to uptake in astroglial primary cultures. Neurochem Res 17, 327–332 (1992). https://doi.org/10.1007/BF00974573

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00974573

Key Words

Navigation