Skip to main content
Log in

Hippocampal loss of the GABAA receptor α1 subunit in patients with chronic pharmacoresistant epilepsies

  • Regular Paper
  • Published:
Acta Neuropathologica Aims and scope Submit manuscript

Abstract

Alterations of gamma aminobutyric acid (GABA)-mediated neurotransmission have been implicated in the pathogenesis of epilepsies. Here we examine the distribution of the GABAA receptor in the hippocampus of 78 surgical specimens from patients with chronic pharmacoresistant focal epilepsies. The receptor was localized immunohistochemically with the monoclonal antibody bd-24 which selectively recognizes the α1 subunit of the GABAA receptor. The results were compared with the receptor distribution of 28 normal hippocampal specimens obtained at autopsy. In the great majority of the surgical specimens a loss of GABAA receptor immunoreactivity was present in CA1 (92.3%), CA4 (78.2%), the dentate granular cell layer (70.5%) and the molecular layer of the dentate gyrus (65.4%). The subiculum revealed a normal staining pattern in all but 4 cases. In no instance did we observe an increase of immunoreactivity in any region or cell population. The decrease of GABAA receptor immunoreactivity was closely related to neuronal loss in the respective specimen and to Ammon's horn sclerosis. There was no correlation between GABAA receptor loss and the patient's age at surgery, duration of seizures, age at onset of seizures and to the presence or absence of secondary generalized tonic clonic seizures. The data suggest that the observed loss of GABAA receptor immunoreactivity is a secondary phenomenon rather than an event that is relevant for the pathogenesis of epileptic seizures.

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. Avoli M (1988) GABAergic mechanisms and epileptic discharges. In: Avoli M, et al (eds) Neurotransmitters and cortical function: from molecules to mind. Plenum Press, New York, pp 187–205

    Google Scholar 

  2. Babb TL (1991) Research on the anatomy and pathology of epileptic tissue. In: Lüders H (ed) Epilepsy surgery. Raven Press, New York, pp 719–727

    Google Scholar 

  3. Babb TL, Pretorius JK, Kupfer WR, Feldblum S (1989) Recovery of decreased glutamate decarboxylase immunoreactivity after rat hippocampal kindling. Epilepsy Res 3: 18–30

    Google Scholar 

  4. Bakay R, Harris A (1981) Neurotransmitter, receptor and biochemical changes in monkey cortical epileptic foci. Brain Res 206: 387–404

    Google Scholar 

  5. Bruton CJ (1988) The neuropathology of temporal lobe epilepsy. Oxford University Press, Oxford

    Google Scholar 

  6. Ewert M, Shivers BD, Lueddens H, Moehler H, Seeburg PH (1990) Subunit selectivity and epitope characterization of mAbs directed against the GABAA/benzodiazepine receptor. J Cell Biol 110: 2043–2048

    Google Scholar 

  7. Franck JE, Kunkel DD, Baskin DG, Schwartzkroin PA (1988) Inhibition in kainate-lesioned hyperexcitable hippocampi: physiologic, autoradiographic, and immunocytochemical observations. J Neurosci 8: 1991–2002

    Google Scholar 

  8. Houser CR (1991) GABA neurons in seizure disorders: a review of immunocytochemical studies. Neurochem Res 16: 295–308

    Google Scholar 

  9. Houser CR, Olsen RW, Richards JG, Möhler H (1988) Immunohistochemical localization of benzodiazepine/GABAA receptors in the human hippocampal formation. J Neurosci 8: 1370–1383

    Google Scholar 

  10. Johnson EW, de Lanerolle NC, Kim JH, Sundaresan S, Spencer DD, Mattson RH, Zoghbi SS, Baldwin RM, Hoffer PB, Seibyl JP, Innis RB (1992) “Central” and “peripheral” benzodiazepine receptors: opposite changes in human epileptogenic tissue. Neurology 42:811–815

    Google Scholar 

  11. Lloyd KG, Munari C, Bossi L, Stoeffels C, Talairach J, Morselli PL (1981) Biochemical evidence for alterations of GABA-mediated synaptic transmission in pathological brain tissue (stereo EEG or morphological definition) from epileptic patients. In: Morselli PL, et al (eds) Neurotransmitters, seizures and epilepsy. Raven Press, New York, pp 325–334

    Google Scholar 

  12. Lloyd KG, Bossi L, Morselli PL Munari C, Rougier M, Loiseau H (1986) Alterations of GABA-mediated synaptic transmission in human epilepsy. Adv Neurol 44: 1033–44

    Google Scholar 

  13. Meencke HJ Veith G (1991) Hippocampal sclerosis in epilepsy. In: Lüders H (ed) Epilepsy surgery. Raven Press, New York, pp 705–715

    Google Scholar 

  14. Olsen RW, Bureau M, Houser CR, Delgado-Escueta AV, Richards JG, Möhler H (1992) GABA/benzodiazepine receptors in human focal epilepsy. Epilepsy Res [suppl] 8: 383–391

    Google Scholar 

  15. Sherwin A, Matthew E, Blain M, Guévremont D (1986) Benzodiazepine receptor binding is not altered in human epiletogenic cortical foci. Neurology 36: 1380–1382

    Google Scholar 

  16. Shivers BD, Killisch I, Sprengel R, Sontheimer H, Köhler M, Schofield PR, Seeburg PH (1989) Two novel GABAA receptor subunits exist in distinct neuronal subpopulations. Neuron 3: 327–337

    Google Scholar 

  17. Sieghard W (1990) GABAA-Benzodiazepinrezeptoren und Epilepsie. Wien Klin Wochenschr 102: 197–201

    Google Scholar 

  18. Snodgrass SR (1992) GABA and epilepsy: their complex relationship and the evolution of our understanding. J Child Neurol 7: 77–86

    Google Scholar 

  19. Valdes F, Dasheiff RM, Birmingham F, Crutcher KA, McNamara JO (1982) Benzodiazepine receptor increases after repeated seizures: evidence for localization to dentate granule cells. Proc Natl Acad Sci USA 79: 193–197

    Google Scholar 

  20. Wisden W, Laurie DJ, Monyer H, Seeburg PH (1992) The distribution of 13 GABAA receptor subunit mRNAs in the rat brain. I. Telencephalon, diencephalon, mesencephalon. J Neurosci 12: 1040–1062

    Google Scholar 

  21. Wolf HK, Campos MG, Zentner J, Hufnagel A, Schramm J, Elger CE, Wiestler OD (1993) Surgical pathology of temporal lobe epilepsy. Exprience with 216 cases. J Neuropathol Exp Neurol 52: 499–506

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Wolf, H.K., Spänle, M., Müller, M.B. et al. Hippocampal loss of the GABAA receptor α1 subunit in patients with chronic pharmacoresistant epilepsies. Acta Neuropathol 88, 313–319 (1994). https://doi.org/10.1007/BF00310375

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00310375

Key words

Navigation