Effects of seizures on developmental processes in the immature brain

Infants and children are at a high risk for seizures compared with adults. Although most seizures in children are benign and result in no long-term consequences, increasing experimental animal data strongly suggest that frequent or prolonged seizures in the developing brain result in long-lasting sequelae. Such seizures may intervene with developmental programmes and lead to inadequate construction of cortical networks rather than induction of neuronal cell loss. As a consequence, the deleterious actions of seizures are strongly age dependent: seizures have different effects on immature or migrating neurons endowed with few synapses and more developed neurons that express hundreds of functional synapses. This differential effect is even more important in human beings and subhuman primates who have an extended brain development period. Seizures also beget seizures during maturation and result in a replay of development programmes, which suggests that epileptogenesis recapitulates ontogenesis. Therefore, to understand seizures and their consequences in the developing brain, it is essential to determine how neuronal activity modulates the main steps of cortical formation. In this Review, we present basic developmental principles obtained from animal studies and examine the long-lasting consequences of epilepsy.

[1]  Y. Ben-Ari,et al.  Involvement of GABAA receptors in the outgrowth of cultured hippocampal neurons , 1993, Neuroscience Letters.

[2]  J. Gaiarsa,et al.  Spontaneous release of GABA activates GABAB receptors and controls network activity in the neonatal rat hippocampus. , 1996, Journal of neurophysiology.

[3]  D B Vigneron,et al.  Seizure-associated brain injury in term newborns with perinatal asphyxia , 2002, Neurology.

[4]  G. Holmes,et al.  Recurrent seizures in immature rats: effect on auditory and visual discrimination. , 1996, Brain research. Developmental brain research.

[5]  Y. Ben‐Ari,et al.  Three-independent-compartment chamber to study in vitro commissural synapses. , 1999, Journal of neurophysiology.

[6]  Y. Ben-Ari,et al.  From seizures to neo‐synaptogenesis: Intrinsic and extrinsic determinants of mossy fiber sprouting in the adult hippocampus , 1994, Hippocampus.

[7]  Epilepsy and Other Chronic Convulsive Diseases , 1882, Edinburgh Medical Journal.

[8]  J. Cavazos,et al.  Synaptic reorganization in the hippocampus induced by abnormal functional activity. , 1988, Science.

[9]  G. Buzsáki,et al.  Early motor activity drives spindle bursts in the developing somatosensory cortex , 2004, Nature.

[10]  Prolonged febrile seizures in the immature rat model enhance hippocampal excitability long term , 2000, Annals of neurology.

[11]  W. Hauser The Prevalence and Incidence of Convulsive Disorders in Children , 1994, Epilepsia.

[12]  J. Velíšková,et al.  Susceptibility of immature and adult brains to seizure effects , 2004, The Lancet Neurology.

[13]  A. Rice,et al.  Status Epilepticus Causes Long‐Term NMDA Receptor‐Dependent Behavioral Changes and Cognitive Deficits , 1998, Epilepsia.

[14]  Y. Ben‐Ari,et al.  Maturation of kainic acid seizure-brain damage syndrome in the rat. i. clinical, electrographic and metabolic observations , 1984, Neuroscience.

[15]  J. Marks,et al.  Vulnerability of CA1 neurons to glutamate is developmentally regulated. , 1996, Brain research. Developmental brain research.

[16]  G. Holmes,et al.  Reduced Neurogenesis after Neonatal Seizures , 2001, The Journal of Neuroscience.

[17]  A. Young,et al.  Differential ontogenic development of three receptors comprising the NMDA receptor/channel complex in the rat hippocampus , 1990, Experimental Neurology.

[18]  Epidemiology of epilepsy in children. , 1995, Cleveland Clinic journal of medicine.

[19]  Y. Ben-Ari,et al.  A Noncanonical Release of GABA and Glutamate Modulates Neuronal Migration , 2005, The Journal of Neuroscience.

[20]  Yehezkel Ben-Ari,et al.  In vitro formation of a secondary epileptogenic mirror focus by interhippocampal propagation of seizures , 2003, Nature Neuroscience.

[21]  G. Holmes,et al.  Synaptic reorganization following kainic acid-induced seizures during development. , 1998, Brain research. Developmental brain research.

[22]  J. MacFall,et al.  Do prolonged febrile seizures produce medial temporal sclerosis? Hypotheses, MRI evidence and unanswered questions. , 2002, Progress in brain research.

[23]  G. Holmes,et al.  New concepts in neonatal seizures. , 2002, Neuroreport.

[24]  C. Frye,et al.  Perforant path stimulation in rats produces seizures, loss of hippocampal neurons, and a deficit in spatial mapping which are reduced by prior MK-801 , 2000, Behavioural Brain Research.

[25]  F. Jensen,et al.  NKCC1 transporter facilitates seizures in the developing brain , 2005, Nature Medicine.

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

[27]  Yehezkel Ben-Ari,et al.  The multiple facets of γ-aminobutyric acid dysfunction in epilepsy: review , 2005, Current opinion in neurology.

[28]  Arnold R. Kriegstein,et al.  Is there more to gaba than synaptic inhibition? , 2002, Nature Reviews Neuroscience.

[29]  Y. Ben‐Ari,et al.  Maturation of kainic acid seizure-brain damage syndrome in the rat. III. Postnatal development of kainic acid binding sites in the limbic system , 1984, Neuroscience.

[30]  K. Holloway,et al.  Human neuronal gamma-aminobutyric acid(A) receptors: coordinated subunit mRNA expression and functional correlates in individual dentate granule cells. , 1999, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[31]  R. Sankar,et al.  GABA metabolism during status epilepticus in the developing rat brain. , 1997, Brain research. Developmental brain research.

[32]  G. Holmes,et al.  Mossy fiber sprouting after recurrent seizures during early development in rats , 1999 .

[33]  T. Baram Long‐term neuroplasticity and functional consequences of single versus recurrent early‐life seizures , 2003, Annals of neurology.

[34]  Karen L. Smith,et al.  Age‐Dependent Alterations in the Operations of Hippocampal Neural Networks a , 1991, Annals of the New York Academy of Sciences.

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

[36]  T. Baram,et al.  Seizure-Induced Neuronal Injury: Vulnerability to Febrile Seizures in an Immature Rat Model , 1998, The Journal of Neuroscience.

[37]  G. Holmes,et al.  Age-dependent effects of glutamate toxicity in the hippocampus. , 1996, Brain research. Developmental brain research.

[38]  J. Velíšková,et al.  Glia activation and cytokine increase in rat hippocampus by kainic acid-induced status epilepticus during postnatal development , 2003, Neurobiology of Disease.

[39]  R. Miles,et al.  On the Origin of Interictal Activity in Human Temporal Lobe Epilepsy in Vitro , 2002, Science.

[40]  B. George,et al.  Kindling model of epilepsy. , 1994, Methods and findings in experimental and clinical pharmacology.

[41]  Y. Ben-Ari,et al.  Giant synaptic potentials in immature rat CA3 hippocampal neurones. , 1989, The Journal of physiology.

[42]  O. Dulac,et al.  Epileptic Encephalopathies: A Brief Overview , 2003, Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society.

[43]  K. Staley,et al.  Transition from Interictal to Ictal Activity in Limbic Networks In Vitro , 2003, The Journal of Neuroscience.

[44]  Michel Le Van Quyen,et al.  Epileptogenic Actions of GABA and Fast Oscillations in the Developing Hippocampus , 2005, Neuron.

[45]  Pablo Lema,et al.  Febrile seizures in the predisposed brain: A new model of temporal lobe epilepsy , 2005, Annals of neurology.

[46]  L. Cowan The epidemiology of the epilepsies in children. , 2002, Mental retardation and developmental disabilities research reviews.

[47]  D. Spencer,et al.  Characteristics of medial temporal lobe epilepsy: I. Results of history and physical examination , 1993, Annals of neurology.

[48]  X. Leinekugel,et al.  A Novel In Vitro Preparation: the Intact Hippocampal Formation , 1997, Neuron.

[49]  G. Mckhann GABA Regulates Synaptic Integration of Newly Generated Neurons in the Adult Brain. , 2006, Neurosurgery.

[50]  Y. Ben-Ari,et al.  Recurrent Mossy Fibers Establish Aberrant Kainate Receptor-Operated Synapses on Granule Cells from Epileptic Rats , 2005, The Journal of Neuroscience.

[51]  Y. Yang,et al.  Neuroprotective effects of brain-derived neurotrophic factor in seizures during development , 1999, Neuroscience.

[52]  M. Poo,et al.  GABA Itself Promotes the Developmental Switch of Neuronal GABAergic Responses from Excitation to Inhibition , 2001, Cell.

[53]  G. Holmes,et al.  Lack of cell loss following recurrent neonatal seizures. , 2002, Brain research. Developmental brain research.

[54]  A. Munnich,et al.  Impaired mitochondrial glutamate transport in autosomal recessive neonatal myoclonic epilepsy. , 2005, American journal of human genetics.

[55]  Y. Ben‐Ari,et al.  Maturation of kainic acid seizure-brain damage syndrome in the rat. II. Histopathological sequelae , 1984, Neuroscience.

[56]  B. Litt,et al.  Temporal lobe epilepsy after experimental prolonged febrile seizures: prospective analysis. , 2006, Brain : a journal of neurology.

[57]  Céline Dubé,et al.  Erratum: Interleukin-1β contributes to the generation of experimental febrile seizures (Annals of Neurology (January 2005) 57 (152-155)) , 2005 .

[58]  P. Stanton,et al.  Resistance of the immature hippocampus to seizure-induced synaptic reorganization. , 1991, Brain research. Developmental brain research.

[59]  N. Ebrahimi,et al.  Two‐Year Remission and Subsequent Relapse in Children with Newly Diagnosed Epilepsy , 2001 .

[60]  Yehezkel Ben-Ari,et al.  The Establishment of GABAergic and Glutamatergic Synapses on CA1 Pyramidal Neurons is Sequential and Correlates with the Development of the Apical Dendrite , 1999, The Journal of Neuroscience.

[61]  G. Holmes,et al.  Consequences of recurrent seizures during early brain development , 1999, Neuroscience.

[62]  G. Holmes,et al.  The Neurobiology and Consequences of Epilepsy in the Developing Brain , 2001, Pediatric Research.

[63]  J. Ellenberg,et al.  Predictors of epilepsy in children who have experienced febrile seizures. , 1976, The New England journal of medicine.

[64]  Y. Ben-Ari,et al.  Consequences of neonatal seizures in the rat: Morphological and behavioral effects , 1998, Annals of neurology.

[65]  P. Bickler,et al.  Journal of Cerebral Blood Flow and Metabolism Developmental Changes in Intracellular Calcium . Regulation in Rat Cerebral Cortex during Hypoxia , 2022 .

[66]  A. Brooks-Kayal,et al.  Long‐term alterations in glutamate receptor and transporter expression following early‐life seizures are associated with increased seizure susceptibility , 2003, Journal of neurochemistry.

[67]  D. Coulter,et al.  Effects of status epilepticus on hippocampal GABAA receptors are age-dependent , 2004, Neuroscience.

[68]  H. Monyer,et al.  NR2A Subunit Expression Shortens NMDA Receptor Synaptic Currents in Developing Neocortex , 1997, The Journal of Neuroscience.

[69]  Chao-Ching Huang,et al.  Febrile seizures impair memory and cAMP response‐element binding protein activation , 2003, Annals of neurology.

[70]  F. Jensen,et al.  Developmental seizures induced by common early-life insults: short- and long-term effects on seizure susceptibility. , 2000, Mental retardation and developmental disabilities research reviews.

[71]  M. Poo,et al.  Modulation of GABAergic Transmission by Activity via Postsynaptic Ca2+-Dependent Regulation of KCC2 Function , 2005, Neuron.

[72]  Karen L. Smith,et al.  Axonal remodeling during postnatal maturation of CA3 hippocampal pyramidal neurons , 1997 .

[73]  J. Burchfiel,et al.  Epileptogenic effect of hypoxia in the immature rodent brain , 1991, Annals of neurology.

[74]  Michel Le Van Quyen,et al.  The dark side of high-frequency oscillations in the developing brain , 2006, Trends in Neurosciences.

[75]  X. Leinekugel,et al.  GABAA, NMDA and AMPA receptors: a developmentally regulated `ménage à trois' , 1997, Trends in Neurosciences.

[76]  I. Scheffer,et al.  Neuronal sodium-channel alpha1-subunit mutations in generalized epilepsy with febrile seizures plus. , 2001, American journal of human genetics.

[77]  Y. Ben-Ari Excitatory actions of gaba during development: the nature of the nurture , 2002, Nature Reviews Neuroscience.

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

[79]  Q. Pittman,et al.  Causal Links between Brain Cytokines and Experimental Febrile Convulsions in the Rat , 2005, Epilepsia.

[80]  E. Delpire Cation-Chloride Cotransporters in Neuronal Communication. , 2000, News in physiological sciences : an international journal of physiology produced jointly by the International Union of Physiological Sciences and the American Physiological Society.

[81]  Ivan Soltesz,et al.  Persistently modified h-channels after complex febrile seizures convert the seizure-induced enhancement of inhibition to hyperexcitability , 2001, Nature Medicine.

[82]  R. Sankar,et al.  Patterns of Status Epilepticus-Induced Neuronal Injury during Development and Long-Term Consequences , 1998, The Journal of Neuroscience.

[83]  S. Shinnar,et al.  Long-term prognosis of seizures with onset in childhood. , 1998, The New England journal of medicine.

[84]  T. Lerer,et al.  Prediction of outcome based on clinical seizure type in newborn infants. , 2002, The Journal of pediatrics.

[85]  Y. Ben-Ari,et al.  Limbic seizure and brain damage produced by kainic acid: Mechanisms and relevance to human temporal lobe epilepsy , 1985, Neuroscience.

[86]  T. Baram,et al.  Developmental Febrile Seizures Modulate Hippocampal Gene Expression of Hyperpolarization-Activated Channels in an Isoform- and Cell-Specific Manner , 2002, The Journal of Neuroscience.

[87]  B. Hermann,et al.  Hippocampal malformation as a cause of familial febrile convulsions and subsequent hippocampal sclerosis. , 1999, Neurology.

[88]  J. Swann,et al.  Penicillin-induced epileptogenesis in immature rat CA3 hippocampal pyramidal cells. , 1984, Brain Research.

[89]  T. Insel,et al.  The ontogeny of excitatory amino acid receptors in the rat forebrain—II. Kainic acid receptors , 1990, Neuroscience.

[90]  G. Holmes Effects of seizures on brain development: lessons from the laboratory. , 2005, Pediatric neurology.

[91]  D. Coulter,et al.  Chronic Epileptogenic Cellular Alterations in the Limbic System After Status Epilepticus , 1999, Epilepsia.

[92]  J. A. Payne,et al.  The K+/Cl− co-transporter KCC2 renders GABA hyperpolarizing during neuronal maturation , 1999, Nature.

[93]  G. Holmes,et al.  Recurrent neonatal seizures: relationship of pathology to the electroencephalogram and cognition. , 2001, Brain research. Developmental brain research.

[94]  Y. Ben-Ari,et al.  Long‐lasting modification of the synaptic properties of rat CA3 hippocampal neurones induced by kainic acid. , 1988, The Journal of physiology.

[95]  I Khalilov,et al.  Early Development of Neuronal Activity in the Primate HippocampusIn Utero , 2001, The Journal of Neuroscience.

[96]  F. Jensen,et al.  Decreased Glutamate Receptor 2 Expression and Enhanced Epileptogenesis in Immature Rat Hippocampus after Perinatal Hypoxia-Induced Seizures , 2001, The Journal of Neuroscience.

[97]  Y. Ben-Ari,et al.  Early expression of KCC2 in rat hippocampal cultures augments expression of functional GABA synapses , 2005, The Journal of physiology.

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

[99]  Y. Ben-Ari,et al.  Glutamate Transporters Prevent the Generation of Seizures in the Developing Rat Neocortex , 2004, The Journal of Neuroscience.

[100]  O. Steward,et al.  Mitochondrial uncoupling protein‐2 protects the immature brain from excitotoxic neuronal death , 2003, Annals of neurology.

[101]  Roustem Khazipov,et al.  Developmental changes in GABAergic actions and seizure susceptibility in the rat hippocampus , 2004, The European journal of neuroscience.

[102]  K. Holloway,et al.  Human Neuronal γ-Aminobutyric AcidA Receptors: Coordinated Subunit mRNA Expression and Functional Correlates in Individual Dentate Granule Cells , 1999, The Journal of Neuroscience.

[103]  Y. Ben-Ari,et al.  Paracrine Intercellular Communication by a Ca2+- and SNARE-Independent Release of GABA and Glutamate Prior to Synapse Formation , 2002, Neuron.

[104]  E. Vining Gaining a perspective on childhood seizures. , 1998, The New England journal of medicine.

[105]  Christophe Bernard,et al.  Newly formed excitatory pathways provide a substrate for hyperexcitability in experimental temporal lobe epilepsy , 1999, The Journal of comparative neurology.

[106]  Y. Ben-Ari,et al.  Anoxia produces smaller changes in synaptic transmission, membrane potential, and input resistance in immature rat hippocampus. , 1989, Journal of neurophysiology.

[107]  M. Patel,et al.  Age dependence of seizure-induced oxidative stress , 2003, Neuroscience.

[108]  G. Holmes,et al.  Age‐Dependent Cognitive and Behavioral Deficits After Kainic Acid Seizures , 1993, Epilepsia.