Parvalbumin- and calbindin-containing neurons express c-fos protein in primary and secondary (mirror) epileptic foci of the rat neocortex

Brain Research

Volumn 761, Issue 1, 1997, Pages 135-145

  Mihaly, Andras ^a   Szente, Magdolna ^b   Dubravcsik, Zsolt ^c   Boda, Bernadett ^c   Kiraly, Erzsebet ^c   Nagy, Tünde ^d   Domonkos, Agota ^d  

^a KUWAIT UNIVERSITY   (Kuwait)

^b UNIVERSITY OF SZEGED   (Hungary)

^c UNIVERSITY OF SZEGED   (Hungary)

^d INSTITUTE OF BIOCHEMISTRY   (Hungary)

Author keywords

Calbindin; Epilepsy; Immediate early gene; Neocortex; Parvalbumin; Rat

Indexed keywords

CALBINDIN; PARVALBUMIN; PROTEIN C FOS;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BRAIN REGION; CONTROLLED STUDY; EPILEPTIC FOCUS; GENE EXPRESSION; IMMEDIATE EARLY GENE; NEOCORTEX; NONHUMAN; PRIORITY JOURNAL; PROTEIN LOCALIZATION; RAT;

ANIMALS; AUTORADIOGRAPHY; BLOTTING, WESTERN; CALCIUM-BINDING PROTEIN, VITAMIN D-DEPENDENT; CEREBRAL CORTEX; ELECTROPHYSIOLOGY; EPILEPSY; GAMMA-AMINOBUTYRIC ACID; MALE; NERVE TISSUE PROTEINS; NEURONS; PARVALBUMINS; PROTO-ONCOGENE PROTEINS C-FOS; RATS; RATS, WISTAR;

EID: 0030835448     PISSN: 00068993     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0006-8993(97)00317-X     Document Type: Article

References (51)

1. Albus K., Wahle P., Lubke J., Matute C. The contribution of GABA-ergic neurons to horizontal intrinsic connections in upper layers of the cat's striate cortex. Exp. Brain Res. 85:1991;235-239.
2. Alcantara S., Ferrer I. Postnatal development of parvalbumin immunoreactivity in the cerebral cortex of the cat. J. Comp. Neurol. 348:1994;133-149.
3. Andressen C., Blumcke I., Celio M.R. Calcium-binding proteins: selective markers of nerve cells. Cell Tissue Res. 271:1993;181-208.
4. Avoli M., Olivier A. Electrophysiological properties and synaptic responses in the deep layers of the human epileptogenic neocortex maintained 'in vitro'. J. Neurophysiol. 61:1989;589-606.
5. Celio M.R. Calbindin D-28k and parvalbumin in the rat nervous system. Neuroscience. 35:1990;375-475.
6. Collins, R.C., Olney, J.W. and Lothman, E.W., Metabolic and pathological consequences of focal seizures. In J.K. Penry and D. Purpura (Eds.), Epilepsy, Raven Press, New York, 1983, pp. 87-107.
7. Creutzfeldt, O.D., Cortex Cerebri. Performance, Structural and Functional Organization of the Cortex, Springer-Verlag, Berlin, 1993, 615 pp.
8. Dragunow M., Currie R.W., Faull R.L.M., Robertson H.A., Jansen K. Immediate-early genes, kindling and long-term potentiation. Neurosci. Biobehav. Rev. 13:1989;301-313.
9. Ebersole J.S., Chatt A.B. Laminar interactions during neocortical epileptogenesis. Brain Res. 298:1984;253-271.
10. Empson R.M., Jefferys J.G. Synaptic inhibition in primary and secondary chronic epileptic foci induced by intrahippocampal tetanus toxin in the rat. J. Physiol. 465:1993;595-614.
11. Ferrer I., Oliver B., Russi A., Casas R., Rivera R. Parvalbumin and calbindin-D28k immunocytochemistry in human neocortical epileptic foci. J. Neurol. Sci. 123:1994;18-25.
12. Ferrer I., Tunon T., Soriano E., del Rio A., Iraizoz I., Fonseca M., Guionnet N. Calbindin immunoreactivity in normal human temporal neocortex. Brain Res. 572:1992;33-41.
13. Gellman R.J., Aghajanian G.K. Pyramidal cells in piriform cortex receive a convergence of inputs from monoamine activated GABAergic interneurons. Brain Res. 600:1993;63-73.
14. Gilbert C.D. Horizontal integration and cortical dynamics. Neuron. 9:1992;1-13.
15. Hancock M.B. DAB-nickel substrate for the differential immunoperoxidase staining of nerve fibers and fiber terminals. J. Histochem. Cytochem. 30:1982;578-579.
16. Herdegen T., Sandkuhler J., Gass P., Kiessling M., Bravo R., Zimmermann M. JUN, FOS, KROX, and CREB transcription factor proteins in the rat cortex: basal expression and induction by spreading depression and epileptic seizures. J. Comp. Neurol. 333:1993;271-288.
17. Howe J.R., Sutor B., Zieglgansberger W. Characteristics of long-duration inhibitory postsynaptic potentials in rat neocortical neurons in vitro. Cell. Mol. Neurobiol. 7:1987;1-18.
18. Jacobson S., Marcus E.M. The laminar distribution of fibers of the corpus callosum: a comparative study in the rat, cat, rhesus monkey and chimpanzee. Brain Res. 24:1970;517-520.
19. Jones, E.G., Anatomy, development and physiology of the corpus callosum. In A.G. Reeves (Ed.), Epilepsy and the Corpus Callosum, Plenum Press, New York, 1985, pp. 3-20.
20. Kisvarday Z.F., Cowey A., Smith A.D., Somogyi P. Interlaminar and lateral excitatory amino acid connections in the striate cortex of monkey. J. Neurosci. 9:1989;667-682.
21. Krnjevic, K., Significance of GABA in brain function. In G. Tunnicliff and B.U. Raess (Eds.), GABA Mechanisms in Epilepsy, Wiley, New York, 1991, pp. 47-48.
22. Kubota Y., Jones E.G. Co-localization of two calcium binding proteins in GABA cells of rat piriform cortex. Brain Res. 600:1993;339-344.
23. Kubota Y., Kawaguchi Y. Three classes of GABAergic interneurons in neocortex and neostriatum. Jpn. J. Physiol. 44(Suppl. 2):1994;145-148.
24. McCormick D.A. GABA as an inhibitory neurotransmitter in human cerebral cortex. J. Neurophysiol. 62:1989;1018-1027.
25. Mihaly, A., Morphological Alterations of Cerebral Cortical Structures in Experimental Aminopyridine Seizures. PhD Thesis, Budapest, 1988, 132 pp.
26. Mihaly A., Bencsik K., Solymosi T. Naltrexone potentiates 4-aminopyridine seizures in the rat. J. Neural Transm. (Gen. Sect.). 79:1990;59-67.
27. Mihaly A., Joo F., Szente M. Neuropathological alterations in the neocortex of rats subjected to focal aminopyridine seizures. Acta Neuropathol. 61:1983;85-94.
28. Mihaly A., Joo F., Szente M. Vasogenic brain edema in focal 4-aminopyridine seizures: the role of neuronal hyperactivity. J. Hirnforsch. 31:1990;77-86.
29. 3H]4-aminopyridine. Acta Neuropathol. 66:1985;145-154.
30. Mody I., Lambert J.D., Heinemann U. Low extracellular magnesium induces epileptiform activity and spreading depression in rat hippocampal slices. J. Neurophysiol. 57:1987;869-888.
31. Morgan J.I., Curran T. Stimulus-transcription coupling in the nervous system: involvement of the inducible proto-oncogenes fos and jun. Annu. Rev. Neurosci. 14:1991;421-451.
32. Morrel, F., Callosal mechanisms in epileptogenesis. Identification of two distinct kinds of spread of epileptic activity. In A.G. Reeves (Ed.), Epilepsy and the Corpus Callosum. Plenum Press, New York, 1985, pp. 99-130.
33. Najlerahim A., Williams S.F., Pearson R.C., Jefferys J.G. Increased expression of GAD mRNA during the chronic epileptic syndrome due to intrahippocampal tetanus toxin. Exp. Brain Res. 90:1992;332-342.
34. Niedermeyer, E., The Epilepsies. Diagnosis and Management, Urban and Schwarzenberg, Munich, 1990, pp. 9-34.
35. Olavarria J., Van Sluyters R.C., Killackey H.P. Evidence for the complementary organization of callosal and thalamic connections within rat somatosensory cortex. Brain Res. 291:1984;364-368.
36. Oliver M.W., Miller J.J. Inhibitory processes of hippocampal CA1 pyramidal neurons following kindling-induced epilepsy in the rat. Can. J. Physiol. Pharmacol. 63:1985;872-878.
37. Perreault P., Avoli A. Effects of low concentrations of 4-aminopyridine on CA1 pyramidal cells of the hippocampus. J. Neurophysiol. 61:1989;953-970.
38. Perreault P., Avoli A. Physiology and pharmacology of epileptiform activity induced by 4-aminopyridine in rat hippocampal slices. J. Neurophysiol. 65:1991;771-785.
39. Ribak C.E., Harris B.A., Vaughn J.E., Roberts E. Inhibitory, GABAergic nerve terminals decrease at sites of focal epilepsy. Science. 205:1979;211-214.
40. Rutecki P.A., Lebeda F.J., Johnston D. 4-Aminopyridine produces epileptiform activity in hippocampus and enhances synaptic excitation and inhibition. J. Neurophysiol. 57:1987;1911-1924.
41. Schwartzkroin P.A., Hugland M.M. Spontaneous rhythmic synchronous activity in epileptic human and normal monkey temporal lobe. Epilepsia. 27:1986;523-533.
42. Segal M. A subset of local interneurons generate slow inhibitory postsynaptic potentials in hippocampal neurons. Brain Res. 511:1990;163-164.
43. Sherwin I. Ictal-interictal unit firing pattern differences in penicillin-induced primary and secondary epileptogenic foci. Exp. Neurol. 84:1984;463-477.
44. Stephan, H., Allocortex, Springer-Verlag, Berlin, 1975, 998 pp.
45. Szentagothai J. The Ferrier Lecture, 1977. The neuron network of the cerebral cortex: a functional interpretation. Proc. R. Soc. Lond. B. 201:1978;219-248.
46. Szente M., Baranyi A. Mechanism of aminopyridine-induced ictal seizure activity in the cat neocortex. Brain Res. 41:1987;373-386.
47. Szente M., Boda B. Cellular mechanisms of neocortical secondary epileptogenesis. Brain Res. 648:1994;203-214.
48. Szente M., Pongracz F. Comparative study of aminopyridine-induced seizure activities in primary and mirror foci of cat's cortex. Electroencephalogr. Clin. Neurophysiol. 52:1981;353-367.
49. Vieira, A., Elkin, R.G. and Kuchler K., Western blotting and ligand blotting using enhanced chemiluminescence and radioiodine detection. In J.E. Celis (Ed.), Cell Biology, A Laboratory Handbook, Vol. 2, Academic Press, San Diego, CA, 1994, pp. 314-321.
50. Wang J.X., Rinzel J. Spindle rhythmicity in the reticular thalami nucleus: synchronization among mutually inhibitory neurons. Neuroscience. 53:1993;899-904.
51. Zilles K., Zilles B., Schleicher A. A quantitative approach to cytoarchitectonics. VI. The areal pattern of the cortex of the albino rat Anat. Embryol. 159:1980;335-360.