Literature DB >> 7903891

Increased expression of GAP-43, somatostatin and neuropeptide Y mRNA in the hippocampus during development of hippocampal kindling in rats.

C Bendotti1, A Vezzani, G Tarizzo, R Samanin.   

Abstract

The expression and distribution of the mRNA coding for the growth-associated protein-43 (GAP-43), a putative marker for neuritic growth, for preprosomatostatin and the preproneuropeptide Y (ppNPY) were analysed in the rat hippocampus during the development of hippocampal kindling by an in situ hybridization technique and computer-assisted grain counting in the cell. The levels of GAP-43 mRNA increased significantly in the CA3 pyramidal neurons and hilar polymorphic neurons of the dentate gyrus 2 days after stage 2 of kindling (preconvulsive stage) but not stage 5 (full seizure expression) in the stimulated hippocampus. The distribution of GAP-43 mRNA was the same in the hippocampus of kindled rats as in sham-stimulated animals. Preprosomatostatin mRNA and ppNPY mRNA contents rose significantly in the hilar polymorphic neurons of the dentate gyrus of the stimulated and contralateral hippocampus at both stages of kindling, with the greatest effect at stage 5. In addition, the number of ppNPY mRNA neurons in the fascia dentata was significantly higher in kindled rats than in controls, but there were no differences in the number of preprosomatostatin mRNA-positive cells. Preprosomatostatin and ppNPY mRNAs were also increased in the neurons of the stratum oriens of the CA1-CA3 subfield of fully kindled animals, whereas at stage 2 only neurons of the CA1 stratum oriens showed a significant increase of preprosomatostatin mRNA. No changes in preprosomatostatin and ppNPY mRNA expression were observed in the various regions of the hippocampus after a single afterdischarge or 1 month after stage 5.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1993        PMID: 7903891     DOI: 10.1111/j.1460-9568.1993.tb00917.x

Source DB:  PubMed          Journal:  Eur J Neurosci        ISSN: 0953-816X            Impact factor:   3.386


  5 in total

1.  Null mutation of c-fos impairs structural and functional plasticities in the kindling model of epilepsy.

Authors:  Y Watanabe; R S Johnson; L S Butler; D K Binder; B M Spiegelman; V E Papaioannou; J O McNamara
Journal:  J Neurosci       Date:  1996-06-15       Impact factor: 6.167

2.  Nerve growth factor accelerates seizure development, enhances mossy fiber sprouting, and attenuates seizure-induced decreases in neuronal density in the kindling model of epilepsy.

Authors:  B Adams; M Sazgar; P Osehobo; C E Van der Zee; J Diamond; M Fahnestock; R J Racine
Journal:  J Neurosci       Date:  1997-07-15       Impact factor: 6.167

3.  Absence of a persistently elevated 37 kDa fos-related antigen and AP-1-like DNA-binding activity in the brains of kainic acid-treated fosB null mice.

Authors:  A Mandelzys; M A Gruda; R Bravo; J I Morgan
Journal:  J Neurosci       Date:  1997-07-15       Impact factor: 6.167

Review 4.  An experimental model of progressive epilepsy: the development of kindling of the hippocampus of the rat.

Authors:  F H Lopes da Silva; W Kamphuis; M Titulaer; M Vreugdenhil; W J Wadman
Journal:  Ital J Neurol Sci       Date:  1995 Feb-Mar

5.  NMDA receptor dependence of kindling and mossy fiber sprouting: evidence that the NMDA receptor regulates patterning of hippocampal circuits in the adult brain.

Authors:  T Sutula; J Koch; G Golarai; Y Watanabe; J O McNamara
Journal:  J Neurosci       Date:  1996-11-15       Impact factor: 6.167

  5 in total

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