Literature DB >> 4027598

Kainic acid-induced seizures: dose-relationship of behavioural, neurochemical and histopathological changes.

G Sperk, H Lassmann, H Baran, F Seitelberger, O Hornykiewicz.   

Abstract

Behavioural, neurochemical and histopathological changes induced by systemic injection of kainic acid were investigated at various doses of the neurotoxin (3, 6 and 10 mg/kg s.c.). There was a positive correlation between the dose of kainic acid and the extent of both the acute neurochemical changes 3 h after the injection (increases of 3,4-dihydroxyphenylacetic acid and 5-hydroxyindoleacetic acid levels and a decrease in noradrenaline levels in all brain regions investigated), the acute histopathological changes (shrinkage and condensation of nerve cells and brain oedema in the entire forebrain) and the extent of behavioural alterations (immobility, 'wet dog shakes' and limbic seizures). However, the slope of the dose-response curves was very steep. Late and irreversible alterations included losses of the enzyme markers glutamic acid decarboxylase and choline acetyltransferase and, histopathologically, incomplete parenchymal necrosis and haemorrhages. These changes, however, were restricted to a few brain regions, the most important being the hippocampus, amygdala, entorhinal and pyriform cortex, and olfactory bulb, and they were seen only in animals which had undergone severe convulsions. It is suggested that the irreversible brain lesions in this animal model of limbic (temporal lobe) epilepsy are not solely induced by a direct action of kainic acid, but may be caused--at least in part--by additional, secondary pathogenetic mechanisms.

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Year:  1985        PMID: 4027598     DOI: 10.1016/0006-8993(85)90159-3

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  28 in total

1.  Microglial Toll-like receptor 2 contributes to kainic acid-induced glial activation and hippocampal neuronal cell death.

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2.  The influence of epileptic neuropathology and prior peripheral immunity on CNS transduction by rAAV2 and rAAV5.

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4.  Age-dependent long-term structural and functional effects of early-life seizures: evidence for a hippocampal critical period influencing plasticity in adulthood.

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Review 6.  Is neuronal death required for seizure-induced epileptogenesis in the immature brain?

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7.  Contrasting features of ERK1/2 activity and synapsin I phosphorylation at the ERK1/2-dependent site in the rat brain in status epilepticus induced by kainic acid in vivo.

Authors:  Yoko Yamagata; Angus C Nairn
Journal:  Brain Res       Date:  2015-08-28       Impact factor: 3.252

8.  Periodic acid-Schiff (PAS)-positive deposits in brain following kainic acid-induced seizures: relationships to fos induction, neuronal necrosis, reactive gliosis, and blood-brain barrier breakdown.

Authors:  S A Bennett; B Stevenson; W A Staines; D C Roberts
Journal:  Acta Neuropathol       Date:  1995       Impact factor: 17.088

9.  Ginseng Rb fraction protects glia, neurons and cognitive function in a rat model of neurodegeneration.

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10.  NP031112, a thiadiazolidinone compound, prevents inflammation and neurodegeneration under excitotoxic conditions: potential therapeutic role in brain disorders.

Authors:  Rosario Luna-Medina; Marta Cortes-Canteli; Susana Sanchez-Galiano; Jose A Morales-Garcia; Ana Martinez; Angel Santos; Ana Perez-Castillo
Journal:  J Neurosci       Date:  2007-05-23       Impact factor: 6.167

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