Elsevier

Neuroscience

Volume 26, Issue 3, September 1988, Pages 763-781
Neuroscience

Protective effects of mossy fiber lesions against kainic acid-induced seizures and neuronal degeneration

https://doi.org/10.1016/0306-4522(88)90097-8Get rights and content

Abstract

The effects of a hippocampal mossy fiber lesion have been determined on neuronal degeneration and limbic seizures provoked by the subsequent intracerebroventricular administration of kainic acid to unanesthetized rats. Mossy fiber lesions were made either by transecting this pathway unilaterally or by destroying the dentate granule cells unilaterally or bilaterally with colchicine. All control rats eventually developed status epilepticus and each temporally discrete seizure that preceded status epilepticus was recorded from the hippocampus ipsilateral to the kainic acid infusion before the contralateral hippocampus. A mossy fiber lesion of the ipsilateral hippocampus prevented the development of status epilepticus in 26% of subjects and in 52% of subjects seizures were recorded from the contralateral hippocampus before the ipsilateral hippocampus. Unlike electrographic records from other treatment groups, those from rats which had received a bilateral colchicine lesion exhibited no consistent pattern indicative of seizure propagation from one limbic region to another. A bilateral, but not a unilateral, mossy fiber lesion also dramatically attenuated the behavioral expression of the seizures. Regardless of its effects on kainic acid-induced electrographic and behavioral seizures, a mossy fiber lesion always substantially reduced or completely prevented the degeneration of ipsilateral hippocampal CA3-CA4 neurons. This protective effect was specific for those hippocampal neurons deprived of mossy fiber innervation. Neurons in other regions of the brain were protected from degeneration only when the mossy fiber lesion also prevented the development of electrographic status epilepticus.

These results suggest that the hippocampal mossy fibers constitute an important, though probably not an obligatory, link in the circuit responsible for the spread of kainic acid seizures. Degeneration of CA3-CA4 neurons appears to depend upon

  • (1)

    the duration of hippocampal seizure activity and

  • (2)

    an as yet undefined influence of or interaction with the mossy fiber projection which enhances the neurodegenerative effect of the seizures.

Reference (55)

  • MonaghanD.T. et al.

    The distribution of [3H]kainic acid binding sites in rat CNS as determined by autoradiography

    Brain Res.

    (1982)
  • NadlerJ.V. et al.

    Use of excitatory amino acids to make axon-sparing lesions of the hypothalamus

  • NiteckaL. et al.

    Maturation of kainic acid seizure-brain damage syndrome in the rat. II. Histopathological sequelae

    Neuroscience

    (1984)
  • OkazakiM.M. et al.

    Mossy fiber lesion reduces the probability that kainic acid will provoke CA3 hippocampal pyramidal cell bursting

    Brain Res.

    (1988)
  • RacineR.J.

    Modification of seizure activity by electrical stimulation. II. Motor seizure

    Electroenceph. clin. Neurophysiol.

    (1972)
  • RepresaA. et al.

    Kainate binding sites in the hippocampal mossy fibers: localization and plasticity

    Neuroscience

    (1987)
  • RobinsonJ.H. et al.

    Kainic acid produces depolarization of CA3 pyramidal cells in the in vitro hippocampal slice

    Brain Res.

    (1981)
  • SawadaS. et al.

    Fast and slow depolarizing potentials induced by short pulses of kainic acid in hippocampal neurons

    Brain Res.

    (1984)
  • SloviterR.S.

    “Epileptic” brain damage in rats induced by sustained electrical stimulation of the perforant path. I. Acute electrophysiological and light microscopic studies

    Brain Res. Bull.

    (1983)
  • UnnerstallJ.R. et al.

    Autoradiographic localization of high affinity [3H]kainic acid binding sites in the rat forebrain

    Eur. J. Pharmac.

    (1983)
  • VicedominiJ.P. et al.

    A model of status epilepticus based on electrical stimulation of hippocampal afferent pathways

    Expl Neurol.

    (1987)
  • WerlingL.L. et al.

    Evidence for differential localization of two binding sites forl-[3H]glutamate in rat fascia dentata

    Brain Res.

    (1983)
  • WestbrookG.L. et al.

    Cellular and synaptic basis of kainic acid-induced hippocampal epileptiform activity

    Brain Res.

    (1983)
  • ZaczekR. et al.

    Kainic acid neurotoxicity and seizures

    Neuropharmacology

    (1981)
  • AitkenP.G. et al.

    Kainic acid inhibits hippocampal cholecystokinin release and has different effects on synaptic transmission in CA3 region of rats and guinea pigs

    Soc. Neurosci. Abstr.

    (1987)
  • AlbertsonT.E. et al.

    Anticonvulsant action of fluzinamide (AHR-8559) on kindled amygdaloid seizures

    Epilepsia

    (1984)
  • AshwoodT.J. et al.

    Intracellular electrophysiology of CA1 pyramidal neurones in slices of the kainic acid lesioned hippocampus of the rat

    Expl Brain Res.

    (1986)
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