Unilateral hippocampal CA3-predominant damage and short latency epileptogenesis after intra-amygdala microinjection of kainic acid in mice

Mesial temporal lobe epilepsy is the most common, intractable seizure disorder in adults. It is associated with an asymmetric pattern of hippocampal neuron loss within the endfolium (hilus and CA3) and CA1, with limited pathology in extra-hippocampal regions. We previously developed a model of focally-evoked seizure-induced neuronal death using intra-amygdala kainic acid (KA) microinjection and characterized the acute hippocampal pathology. Here, we sought to characterize the full extent of hippocampal and potential extra-hippocampal damage in this model, and the temporal onset of epileptic seizures. Seizure damage assessed at four stereotaxic levels by FluoroJade B staining was most prominent in ipsilateral hippocampal CA3 where it extended from septal to temporal pole. Minor but significant neuronal injury was present in ipsilateral CA1. Extra-hippocampal neuronal damage was generally limited in extent and restricted to the lateral septal nucleus, injected amygdala and select regions of neocortex ipsilateral to the seizure elicitation side. Continuous surface EEG recorded with implanted telemetry units in freely-moving mice detected spontaneous, epileptic seizures by five days post-KA in all mice. Epileptic seizure number averaged 1-4 per day. Hippocampi from epileptic mice 15 days post-KA displayed unilateral CA3 lesions, astrogliosis and increased neuropeptide Y immunoreactivity suggestive of mossy fiber rearrangement. These studies characterize a mouse model of unilateral hippocampal-dominant neuronal damage and short latency epileptogenesis that may be suitable for studying the cell and molecular pathogenesis of human mesial temporal lobe epilepsy.

[1]  毛利 元信 Unilateral hippocampal CA3-predominant damage and short latency epileptogenesis after intra-amygdala microinjection of kainic acid in mice , 2010 .

[2]  A. Pitkänen,et al.  Administration of diazepam during status epilepticus reduces development and severity of epilepsy in rat , 2005, Epilepsy Research.

[3]  大溪 幸子,et al.  Bim regulation may determine hippocampal vulnerability after injurious seizures and in temporal lobe epilepsy , 2005 .

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

[5]  H. Duvernoy,et al.  Hippocampal anatomy and hippocampal sclerosis , 2005 .

[6]  R. Palmiter,et al.  Knock-Out Mice Reveal a Critical Antiepileptic Role for Neuropeptide Y , 1997, The Journal of Neuroscience.

[7]  R. Simon,et al.  Development of a model of seizure‐induced hippocampal injury with features of programmed cell death in the BALB/c mouse , 2004, Journal of neuroscience research.

[8]  Simon Shorvon,et al.  Treatment of Epilepsy , 2004 .

[9]  Tatsuya Tanaka,et al.  Long-term observation of rats after unilateral intra-amygdaloid injection of kainic acid , 1988, Brain Research.

[10]  R. Dingledine,et al.  Neuronal and glial pathological changes during epileptogenesis in the mouse pilocarpine model , 2003, Experimental Neurology.

[11]  C. Cepeda,et al.  Spontaneous secondarily generalized seizures induced by a single microinjection of kainic acid into unilateral amygdala in cats. , 1985, Electroencephalography and clinical neurophysiology.

[12]  Andrew M. White,et al.  Development of Spontaneous Seizures after Experimental Status Epilepticus: Implications for Understanding Epileptogenesis , 2007, Epilepsia.

[13]  F. Dudek,et al.  Functional significance of hippocampal plasticity in epileptic brain: Electrophysiological changes of the dentate granule cells associated with mossy fiber sprouting , 1994, Hippocampus.

[14]  J. Nadler,et al.  Spontaneous Release of Neuropeptide Y Tonically Inhibits Recurrent Mossy Fiber Synaptic Transmission in Epileptic Brain , 2005, The Journal of Neuroscience.

[15]  A. Pitkänen,et al.  Status Epilepticus Causes Necrotic Damage in the Mediodorsal Nucleus of the Thalamus in Immature Rats , 2001, The Journal of Neuroscience.

[16]  O. Steward,et al.  Genetic determinants of susceptibility to excitotoxic cell death: implications for gene targeting approaches. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[17]  R. S. Sloviter “Epileptic” brain damage in rats induced by sustained electrical stimulation of the perforant path. I. Acute electrophysiological and light microscopic studies , 1983, Brain Research Bulletin.

[18]  G. Sperk,et al.  Functional changes in somatostatin and neuropeptide Y containing neurons in the rat hippocampus in chronic models of limbic seizures , 1996, Epilepsy Research.

[19]  B. Meldrum Implications for neuroprotective treatments. , 2002, Progress in brain research.

[20]  R. S. Sloviter,et al.  Hippocampal granule cell activity and c‐Fos expression during spontaneous seizures in awake, chronically epileptic, pilocarpine‐treated rats: Implications for hippocampal epileptogenesis , 2005, The Journal of comparative neurology.

[21]  J. Prehn,et al.  Bcl-w protects hippocampus during experimental status epilepticus. , 2007, The American journal of pathology.

[22]  D. Margineanu,et al.  Pilocarpine-induced epileptogenesis in the rat: Impact of initial duration of status epilepticus on electrophysiological and neuropathological alterations , 2002, Epilepsy Research.

[23]  F. D. da Silva,et al.  Altered hippocampal gene expression prior to the onset of spontaneous seizures in the rat post‐status epilepticus model , 2001, The European journal of neuroscience.

[24]  Margaret Fahnestock,et al.  Kindling and status epilepticus models of epilepsy: rewiring the brain , 2004, Progress in Neurobiology.

[25]  D. Fujikawa,et al.  Status Epilepticus–Induced Neuronal Loss in Humans Without Systemic Complications or Epilepsy , 2000, Epilepsia.

[26]  W. Löscher,et al.  N-methyl-d-aspartate receptor blockade after status epilepticus protects against limbic brain damage but not against epilepsy in the kainate model of temporal lobe epilepsy , 2003, Neuroscience.

[27]  R. Fariello,et al.  Potentiation of kainic acid epileptogenicity and sparing from neuronal damage by an NMDA receptor antagonist , 1989, Epilepsy Research.

[28]  G. Sperk,et al.  Somatostatin, neuropeptide Y, neurokinin B and cholecystokinin immunoreactivity in two chronic models of temporal lobe epilepsy , 1995, Neuroscience.

[29]  R. Simon,et al.  Spatio-temporal profile of DNA fragmentation and its relationship to patterns of epileptiform activity following focally evoked limbic seizures , 2000, Brain Research.

[30]  R. S. Sloviter The neurobiology of temporal lobe epilepsy: too much information, not enough knowledge. , 2005, Comptes rendus biologies.

[31]  M. Thom,et al.  Quantitative Neuropathology of the Entorhinal Cortex Region in Patients with Hippocampal Sclerosis and Temporal Lobe Epilepsy , 2005, Epilepsia.

[32]  P. J. Larsen,et al.  Powerful inhibition of kainic acid seizures by neuropeptide Y via Y5-like receptors , 1997, Nature Medicine.

[33]  G. Sperk,et al.  Seizure susceptibility and epileptogenesis are decreased in transgenic rats overexpressing neuropeptide Y , 2002, Neuroscience.

[34]  D. Riche,et al.  Sustained limbic seizures induced by intraamygdaloid kainic acid in the baboon: Symptomatology and neuropathological consequences , 1980, Annals of neurology.

[35]  A. Pitkänen,et al.  Is mossy fiber sprouting present at the time of the first spontaneous seizures in rat experimental temporal lobe epilepsy? , 2001, Hippocampus.

[36]  R. Sankar,et al.  Substance P is expressed in hippocampal principal neurons during status epilepticus and plays a critical role in the maintenance of status epilepticus. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[37]  D. Geschwind,et al.  Dentate Granule Cell Neurogenesis Is Increased by Seizures and Contributes to Aberrant Network Reorganization in the Adult Rat Hippocampus , 1997, The Journal of Neuroscience.

[38]  O. P. Ottersen,et al.  Injections of kainic acid into the amygdaloid complex of the rat: An electrographic, clinical and histological study in relation to the pathology of epilepsy , 1980, Neuroscience.

[39]  Shigeyoshi Itohara,et al.  Adenosine kinase is a target for the prediction and prevention of epileptogenesis in mice. , 2008, The Journal of clinical investigation.

[40]  A. Vezzani,et al.  Enhanced neuropeptide Y release in the hippocampus is associated with chronic seizure susceptibility in kainic acid treated rats , 1994, Brain Research.

[41]  R. S. Sloviter,et al.  Translamellar Disinhibition in the Rat Hippocampal Dentate Gyrus after Seizure-Induced Degeneration of Vulnerable Hilar Neurons , 2004, The Journal of Neuroscience.

[42]  S A Deadwyler,et al.  Neuronal Hypertrophy in the Neocortex of Patients with Temporal Lobe Epilepsy , 2001, The Journal of Neuroscience.

[43]  J. Thornton,et al.  Rapid stereological quantitation of temporal neocortex in TLE. , 2003, Magnetic resonance imaging.

[44]  T. Halonen,et al.  Status epilepticus-induced neuronal damage in the rat amygdaloid complex: distribution, time-course and mechanisms , 1999, Neuroscience.

[45]  R. Simon,et al.  Activation of Bcl-2-Associated Death Protein and Counter-Response of Akt within Cell Populations during Seizure-Induced Neuronal Death , 2002, The Journal of Neuroscience.

[46]  D. Treiman,et al.  Hippocampal Pyramidal Cell Loss in Human Status Epilepticus , 1992, Epilepsia.

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

[48]  Bret N. Smith,et al.  Pilocarpine-induced status epilepticus results in mossy fiber sprouting and spontaneous seizures in C57BL/6 and CD-1 mice , 2002, Epilepsy Research.

[49]  R. Simon,et al.  Characterization of neuronal death induced by focally evoked limbic seizures in the C57BL/6 mouse , 2002, Journal of neuroscience research.

[50]  F. Dudek,et al.  Electrographic Seizures and New Recurrent Excitatory Circuits in the Dentate Gyrus of Hippocampal Slices from Kainate-Treated Epileptic Rats , 1996, The Journal of Neuroscience.

[51]  George Paxinos,et al.  The Mouse Brain in Stereotaxic Coordinates , 2001 .

[52]  J. Fritschy,et al.  Seizure Suppression by Adenosine A1 Receptor Activation in a Mouse Model of Pharmacoresistant Epilepsy , 2003, Epilepsia.

[53]  H. Kudrimoti,et al.  On the relevance of prolonged convulsive status epilepticus in animals to the etiology and neurobiology of human temporal lobe epilepsy , 2007, Epilepsia.

[54]  A. Vezzani,et al.  Interleukin-1β Immunoreactivity and Microglia Are Enhanced in the Rat Hippocampus by Focal Kainate Application: Functional Evidence for Enhancement of Electrographic Seizures , 1999, The Journal of Neuroscience.

[55]  Philip A. Williams,et al.  Reassessment of the effects of cycloheximide on mossy fiber sprouting and epileptogenesis in the pilocarpine model of temporal lobe epilepsy. , 2002, Journal of neurophysiology.

[56]  J. Engel Mesial Temporal Lobe Epilepsy: What Have We Learned? , 2001, The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry.

[57]  Marco Weiergräber,et al.  Electrocorticographic and deep intracerebral EEG recording in mice using a telemetry system. , 2005, Brain research. Brain research protocols.

[58]  Asla Pitkänen,et al.  Epileptogenesis in Experimental Models , 2007, Epilepsia.

[59]  W T Blume,et al.  Amygdaloid sclerosis in temporal lobe epilepsy , 1993, Annals of neurology.

[60]  G. Sperk,et al.  Anticonvulsant and Antiepileptogenic Effects Mediated by Adeno-Associated Virus Vector Neuropeptide Y Expression in the Rat Hippocampus , 2004, The Journal of Neuroscience.

[61]  P. Jedlicka,et al.  Excitotoxic hippocampal neuron loss following sustained electrical stimulation of the perforant pathway in the mouse , 2006, Brain Research.

[62]  Asla Pitkänen,et al.  A new model of chronic temporal lobe epilepsy induced by electrical stimulation of the amygdala in rat , 2000, Epilepsy Research.

[63]  A. Pitkänen,et al.  Administration of caspase 3 inhibitor during and after status epilepticus in rat: effect on neuronal damage and epileptogenesis , 2003, Neuropharmacology.