A new model of chronic temporal lobe epilepsy induced by electrical stimulation of the amygdala in rat

Spontaneous seizures are the hallmark of human epilepsy but they do not occur in most of the epilepsy models that are used to investigate the mechanisms of epilepsy or to test new antiepileptic compounds. This study was designed to develop a new focal epilepsy model that mimics different aspects of human temporal lobe epilepsy (TLE), including the occurrence of spontaneous seizures. Self-sustained status epilepticus (SSSE) lasting for 6-20 h was induced by a 20-30 min stimulation of the lateral nucleus of the amygdala (100 ms train of 1 ms, 60 Hz bipolar pulses, 400 microA, every 0.5 s). Stimulated rats (n = 16) were monitored with a video-EEG recording system every other day (24 h/day) for 6 months, and every other video-EEG recording was analyzed. Spontaneous epileptic seizures (total number 3698) were detected in 13 of the 15 animals (88%) after a latency period of 6 to 85 days (median 33 days). Four animals (31%) had frequent (697-1317) seizures and 9 animals (69%) had occasional seizures (1-107) during the 6-months follow-up period. Fifty-seven percent of the seizures occurred during daytime (lights on 07:00-19:00 h). At the end of the follow-up period, epileptic animals demonstrated impaired spatial memory in the Morris water-maze. Histologic analysis indicated neuronal loss in the amygdala, hippocampus, and surrounding cortical areas, and mossy fiber sprouting in the dentate gyrus. The present data indicate that focal stimulation of the amygdala initiates a cascade of events that lead to the development of spontaneous seizures in rats. This model provides a new tool to better mimic different aspects of human TLE for investigation of the pathogenesis of TLE or the effects of new antiepileptic compounds on status epilepticus, epileptogenesis, and spontaneous seizures.

[1]  T. Halonen,et al.  Tiagabine prevents seizures, neuronal damage and memory impairment in experimental status epilepticus. , 1996, European journal of pharmacology.

[2]  G. Holmes,et al.  Kainic acid seizures in the developing brain: status epilepticus and spontaneous recurrent seizures. , 1992, Brain research. Developmental brain research.

[3]  G. Plazzi,et al.  Partial Epilepsy of Long Duration: Changing Semiology with Age , 1996, Epilepsia.

[4]  T. Babb,et al.  In contrast to kindled seizures, the frequency of spontaneous epilepsy in the limbic status model correlates with greater aberrant fascia dentata excitatory and inhibitory axon sprouting, and increased staining for N-methyl-d-aspartate, AMPA and GABAA receptors , 1997, Neuroscience.

[5]  D. Hosford,et al.  Differences in the anatomic distribution of immediate-early gene expression in amygdala and angular bundle kindling development , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[6]  Asla Pitkänen,et al.  Amygdala damage in experimental and human temporal lobe epilepsy , 1998, Epilepsy Research.

[7]  E. Bertram Functional Anatomy of Spontaneous Seizures in a Rat Model of Limbic Epilepsy , 1997, Epilepsia.

[8]  L F Quesney,et al.  Clinical and EEG Features of Complex Partial Seizures of Temporal Lobe Origin , 1986, Epilepsia.

[9]  Joseph E LeDoux,et al.  Organization of intra-amygdaloid circuitries in the rat: an emerging framework for understanding functions of the amygdala , 1997, Trends in Neurosciences.

[10]  Robert S. Fisher,et al.  Animal models of the epilepsies , 1989, Brain Research Reviews.

[11]  J Gotman,et al.  Relations Between EEG Seizure Morphology, Interhemispheric Spread, and Mesial Temporal Atrophy in Bitemporal Epilepsy , 1997, Epilepsia.

[12]  E. Wyllie,et al.  The Treatment of Epilepsy: Principles and Practice , 1997 .

[13]  H. Romijn,et al.  Hypoxic-ischemic encephalopathy sustained in early postnatal life may result in permanent epileptic activity and an altered cortical convulsive threshold in rat , 1994, Epilepsy Research.

[14]  T. Halonen,et al.  Subiculum, presubiculum and parasubiculum have different sensitivities to seizure-induced neuronal damage in the rat , 1995, Neuroscience Letters.

[15]  A. Obenaus,et al.  Dentate granule cells form novel basal dendrites in a rat model of temporal lobe epilepsy , 1998, Neuroscience.

[16]  R. Schwarcz,et al.  Preferential neuronal loss in layer III of the medial entorhinal cortex in rat models of temporal lobe epilepsy , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[17]  W H Theodore,et al.  The secondarily generalized tonic‐clonic seizure , 1994, Neurology.

[18]  E. Cavalheiro,et al.  Developmental aspects of the pilocarpine model of epilepsy , 1996, Epilepsy Research.

[19]  E. Cavalheiro,et al.  Spontaneous Recurrent Seizures in Rats: Amino Acid and Monoamine Determination in the Hippocampus , 1994, Epilepsia.

[20]  A. Represa,et al.  Long‐lasting enhanced expression in the rat hippocampus of NMDAR1 splice variants in a kainate model of epilepsy , 1998, The European journal of neuroscience.

[21]  R. Insausti,et al.  The human entorhinal cortex: A cytoarchitectonic analysis , 1995, The Journal of comparative neurology.

[22]  T L Babb,et al.  Hippocampal EEG excitability and chronic spontaneous seizures are associated with aberrant synaptic reorganization in the rat intrahippocampal kainate model. , 1993, Electroencephalography and clinical neurophysiology.

[23]  F. Morrell,et al.  Secondary Epileptogenesis and Brain Tumors , 1999 .

[24]  F. Edward Dudek,et al.  Recurrent spontaneous motor seizures after repeated low-dose systemic treatment with kainate: assessment of a rat model of temporal lobe epilepsy , 1998, Epilepsy Research.

[25]  Edward H Bertram,et al.  Self-sustaining limbic status epilepticus induced by ‘continuous’ hippocampal stimulation: electrographic and behavioral characteristics , 1989, Epilepsy Research.

[26]  E. Bertram,et al.  The evolution of a rat model of chronic spontaneous limbic seizures , 1994, Brain Research.

[27]  T. Babb,et al.  Circuit Mechanisms of Seizures in the Pilocarpine Model of Chronic Epilepsy: Cell Loss and Mossy Fiber Sprouting , 1993, Epilepsia.

[28]  Wolfgang Löscher,et al.  Animal models of intractable epilepsy , 1997, Progress in Neurobiology.

[29]  E. Bertram,et al.  The ontogeny of seizures in a rat model of limbic epilepsy: evidence for a kindling process in the development of chronic spontaneous seizures , 1993, Brain Research.

[30]  T. Halonen,et al.  Status Epilepticus Causes Selective Regional Damage and Loss of GABAergic Neurons in the Rat Amygdaloid Complex , 1996, The European journal of neuroscience.

[31]  R. Racine,et al.  Modification of seizure activity by electrical stimulation. II. Motor seizure. , 1972, Electroencephalography and clinical neurophysiology.

[32]  L F Quesney,et al.  Depth electrode investigations in patients with bitemporal epileptiform abnormalities , 1989, Annals of neurology.

[33]  P. Gloor,et al.  Quantitative evaluation of neuronal loss in the dorsal hippocampus in rats with long-term pilocarpine seizures , 1994, Epilepsy Research.

[34]  W. Hauser,et al.  Seizure recurrence after a 1st unprovoked seizure: An extended follow-up , 2011, Neurology.

[35]  G. Golarai,et al.  Mossy fiber synaptic reorganization induced by kindling: time course of development, progression, and permanence , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[36]  D. Naritoku,et al.  Seizures, epilepsy, and functional recovery after traumatic brain injury , 1997, Neurology.

[37]  C. Wasterlain,et al.  Chronic epileptogenicity following focal status epilepticus , 1994, Brain Research.

[38]  T. Freund,et al.  Delayed cell death in the contralateral hippocampus following kainate injection into the CA3 subfield , 1995, Neuroscience.

[39]  H. Lüders,et al.  The Epilepsies Etiologies and prevention , 1999 .

[40]  A. Beaudet,et al.  Automated EEG Monitoring in Defining a Chronic Epilepsy Model , 1994, Epilepsia.

[41]  R. Schwarcz,et al.  Aminooxyacetic acid causes selective neuronal loss in layer III of the rat medial entorhinal cortex , 1992, Neuroscience Letters.

[42]  Elly Nedivi,et al.  Numerous candidate plasticity-related genes revealed by differential cDNA cloning , 1993, Nature.

[43]  D. Prince,et al.  Inhibitory function in two models of chronic epileptogenesis , 1998, Epilepsy Research.

[44]  CR Houser,et al.  Altered patterns of dynorphin immunoreactivity suggest mossy fiber reorganization in human hippocampal epilepsy , 1990, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[45]  E. Cavalheiro,et al.  Effects of conventional antiepileptic drugs in a model of spontaneous recurrent seizures in rats , 1995, Epilepsy Research.

[46]  N. Fountain,et al.  Functional anatomy of limbic epilepsy: a proposal for central synchronization of a diffusely hyperexcitable network , 1998, Epilepsy Research.

[47]  Z. Bortolotto,et al.  Spontaneous recurrent seizures in rats: An experimental model of partial epilepsy , 1990, Neuroscience & Biobehavioral Reviews.

[48]  P. Andersen,et al.  Spatial learning impairment parallels the magnitude of dorsal hippocampal lesions, but is hardly present following ventral lesions , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[49]  D. Fujikawa The temporal evolution of neuronal damage from pilocarpine-induced status epilepticus , 1996, Brain Research.

[50]  R. Ellenbogen,et al.  Posttraumatic Epilepsy Prevention , 1999 .

[51]  R. S. Sloviter,et al.  A simplified timm stain procedure compatible with formaldehyde fixation and routine paraffin embedding of rat brain , 1982, Brain Research Bulletin.

[52]  J. Wada,et al.  Evidence of Secondary Epileptogenesis in Amygdaloid Overkindled Cats: Electroclinical Documentation of Spontaneous Seizures , 1993, Epilepsia.

[53]  G. Paxinos The Rat nervous system , 1985 .

[54]  J. L. Stringer,et al.  Recurrent spontaneous hippocampal seizures in the rat as a chronic sequela to limbic status epilepticus , 1990, Epilepsy Research.

[55]  R. Schwarcz,et al.  Preferential neuronal loss in layer III of the entorhinal cortex in patients with temporal lobe epilepsy , 1993, Epilepsy Research.

[56]  D. Treiman,et al.  A progressive sequence of electroencephalographic changes during generalized convulsive status epilepticus , 1990, Epilepsy Research.

[57]  R. Sankar,et al.  Time-dependent decrease in the effectiveness of antiepileptic drugs during the course of self-sustaining status epilepticus , 1998, Brain Research.

[58]  Asla Pitkänen,et al.  Remodeling of neuronal circuitries in human temporal lobe epilepsy: Increased expression of highly polysialylated neural cell adhesion molecule in the hippocampus and the entorhinal cortex , 1998, Annals of neurology.

[59]  Z. Bortolotto,et al.  Long‐Term Effects of Pilocarpine in Rats: Structural Damage of the Brain Triggers Kindling and Spontaneous I Recurrent Seizures , 1991, Epilepsia.

[60]  F. Dudek,et al.  Chronic seizures and collateral sprouting of dentate mossy fibers after kainic acid treatment in rats , 1988, Brain Research.

[61]  A. Pitkänen,et al.  Projections from the lateral, basal, and accessory basal nuclei of the amygdala to the hippocampal formation in rat , 1999, The Journal of comparative neurology.

[62]  G. V. Goddard,et al.  A permanent change in brain function resulting from daily electrical stimulation. , 1969, Experimental neurology.

[63]  G. Paxinos,et al.  The Rat Brain in Stereotaxic Coordinates , 1983 .

[64]  Martin Straume,et al.  Temporal distribution of partial seizures: Comparison of an animal model with human partial epilepsy , 1998, Annals of neurology.

[65]  M. Witter,et al.  Entorhinal cortex of the rat: Cytoarchitectonic subdivisions and the origin and distribution of cortical efferents , 1998, Hippocampus.

[66]  G. D'Amico,et al.  Natural History and Prognosis , 1987 .

[67]  R. Schwarcz,et al.  Neuronal damage after the injection of amino-oxyacetic acid into the rat entorhinal cortex: a silver impregnation study , 1997, Neuroscience.