Literature DB >> 2272341

Use of maximal dentate activation to study the effect of drugs on kindling and kindled responses.

J L Stringer1, E W Lothman.   

Abstract

Maximal dentate activation is a paroxysmal event characterized by the appearance of bursts of large amplitude population spikes in the dentate gyrus that has been shown to be associated with the production of afterdischarges in limbic circuits. Repeated elicitation of maximal dentate activation in the anesthetized rat produces a progressive increase in afterdischarge duration. The present work examined the role of NMDA receptor activation in this process. The effects of MK-801 (a systemically active NMDA receptor complex antagonist) and imipramine and desipramine (tricyclic antidepressants recently reported to have NMDA receptor-coupled channel blocking properties) were studied. MK-801, at 0.5 mg/kg, prevented the lengthening of the duration of maximal dentate activation. At 2 mg/kg, MK-801 also shortened the duration of maximal dentate activation already established. Imipramine showed a similar dose-dependent response pattern with 15 mg/kg and 50 mg/kg respectively. Desipramine (50 mg/kg) was similar to imipramine (50 mg/kg) in its effect. Thus, the drugs studied were effective at shortening limbic epileptiform discharges. These results support the use of this model to examine drug effects and strengthen the hypothesis that NMDA receptors play a critical role in seizure generation in the limbic system and, specifically, in the lengthening of the duration of maximal dentate activation.

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Year:  1990        PMID: 2272341     DOI: 10.1016/0920-1211(90)90071-3

Source DB:  PubMed          Journal:  Epilepsy Res        ISSN: 0920-1211            Impact factor:   3.045


  4 in total

1.  Drug refractory epilepsy in brain damage: effect of dextromethorphan on EEG in four patients.

Authors:  B Schmitt; R Netzer; S Fanconi; P Baumann; E Boltshauser
Journal:  J Neurol Neurosurg Psychiatry       Date:  1994-03       Impact factor: 10.154

2.  In the hippocampus in vivo, nitric oxide does not appear to function as an endogenous antiepileptic agent.

Authors:  J L Stringer; F Erden
Journal:  Exp Brain Res       Date:  1995       Impact factor: 1.972

3.  High dose of 8-OH-DPAT decreases maximal dentate gyrus activation and facilitates granular cell plasticity in vivo.

Authors:  Gergely Orban; Massimo Pierucci; Arcangelo Benigno; Mauro Pessia; Salvatore Galati; Mario Valentino; Richard Muscat; Giuseppe Di Giovanni
Journal:  Exp Brain Res       Date:  2013-06-19       Impact factor: 1.972

4.  The FAAH inhibitor URB597 suppresses hippocampal maximal dentate afterdischarges and restores seizure-induced impairment of short and long-term synaptic plasticity.

Authors:  Roberto Colangeli; Massimo Pierucci; Arcangelo Benigno; Giuseppe Campiani; Stefania Butini; Giuseppe Di Giovanni
Journal:  Sci Rep       Date:  2017-09-11       Impact factor: 4.379

  4 in total

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