The neurobiology of epilepsy

Epilepsy is a complex disease with diverse clinical characteristics that preclude a singular mechanism. One way to gain insight into potential mechanisms is to reduce the features of epilepsy to its basic components: seizures, epileptogenesis, and the state of recurrent unprovoked seizures that defines epilepsy itself. A common way to explain seizures in a normal individual is that a disruption has occurred in the normal balance of excitation and inhibition. The fact that multiple mechanisms exist is not surprising given the varied ways the normal nervous system controls this balance. In contrast, understanding seizures in the brain of an individual with epilepsy is more difficult because seizures are typically superimposed on an altered nervous system. The different environment includes diverse changes, making mechanistic predictions a challenge. Understanding the mechanisms of seizures in an individual with epilepsy is also more complex than understanding the mechanisms of seizures in a normal individual because epilepsy is not necessarily a static condition but can continue to evolve over the lifespan. Using temporal lobe epilepsy as an example, it is clear that genes, developmental mechanisms, and neuronal plasticity play major roles in creating a state of underlying hyperexcitability. However, the critical control points for the emergence of chronic seizures in temporal lobe epilepsy, as well as their persistence, frequency, and severity, are questions that remain unresolved.

[1]  S Lehéricy,et al.  Developmental abnormalities of the medial temporal lobe in patients with temporal lobe epilepsy. , 1995, AJNR. American journal of neuroradiology.

[2]  Karen L. Smith,et al.  Structural and functional asymmetry in the normal and epileptic rat dentate gyrus , 2002, The Journal of comparative neurology.

[3]  A. Hodgkin,et al.  Propagation of electrical signals along giant nerve fibres , 1952, Proceedings of the Royal Society of London. Series B - Biological Sciences.

[4]  P. Somogyi,et al.  Synchronization of neuronal activity in hippocampus by individual GABAergic interneurons , 1995, Nature.

[5]  P. Schwartzkroin,et al.  Developmental and regional differences in the localization of Na,K-ATPase activity in the rabbit hippocampus , 1985, Brain Research.

[6]  G. Somjen Ion Regulation in the Brain: Implications for Pathophysiology , 2002, The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry.

[7]  B. MacVicar,et al.  Modulation of neuronal excitability by astrocytes. , 1999, Advances in neurology.

[8]  B. Hille Ionic channels of excitable membranes , 2001 .

[9]  H. Scharfman,et al.  Growth factors and epilepsy , 2005 .

[10]  R. Ottman Analysis of Genetically Complex Epilepsies , 2005, Epilepsia.

[11]  J. Jackson,et al.  EPILEPTIC ATTACKS WITH A WARNING OF A CRUDE SENSATION OF SMELL AND WITH THE INTELLECTUAL AURA (DREAMY STATE) IN A PATIENT WHO HAD SYMPTOMS POINTING TO GROSS ORGANIC DISEASE OF THE RIGHT TEMPORO-SPHENOIDAL LOBE , 1899 .

[12]  Meldrum Bs First Alfred Meyer Memorial Lecture. Epileptic brain damage: a consequence and a cause of seizures , 1997 .

[13]  R. Traub,et al.  Gap junctions, fast oscillations and the initiation of seizures. , 2004, Advances in experimental medicine and biology.

[14]  Renzo Guerrini,et al.  Epileptic Syndromes and Visually Induced Seizures , 2004, Epilepsia.

[15]  A. Pitkänen,et al.  Animal models of post-traumatic epilepsy. , 2006, Journal of neurotrauma.

[16]  A. Pitkänen,et al.  Large-Scale Analysis of Gene Expression in Epilepsy Research: Is Synthesis Already Possible? , 2004, Neurochemical Research.

[17]  T. Fellin,et al.  Do astrocytes contribute to excitation underlying seizures? , 2005, Trends in molecular medicine.

[18]  Michael Frotscher,et al.  Kainic acid‐induced recurrent mossy fiber innervation of dentate gyrus inhibitory interneurons: Possible anatomical substrate of granule cell hyperinhibition in chronically epileptic rats , 2006, The Journal of comparative neurology.

[19]  H. Jasper,et al.  Epilepsy and the functional anatomy of the human brain , 1985 .

[20]  T. Baram,et al.  Febrile seizures and mechanisms of epileptogenesis: insights from an animal model. , 2004, Advances in experimental medicine and biology.

[21]  T. Baram,et al.  Interleukin‐1β contributes to the generation of experimental febrile seizures , 2005, Annals of neurology.

[22]  M C Walker,et al.  Disease modification in partial epilepsy. , 2002, Brain : a journal of neurology.

[23]  S Lehéricy,et al.  Hippocampal developmental changes in patients with partial epilepsy: Magnetic resonance imaging and clinical aspects , 1998, Annals of neurology.

[24]  John R. Huguenard,et al.  Electrophysiology of the Neuron: An Interactive Tutorial , 1994 .

[25]  C. Bazil Sleep disturbances in epilepsy patients , 2005, Current neurology and neuroscience reports.

[26]  R Ottman,et al.  Identification of epilepsy genes in human and mouse. , 2001, Annual review of genetics.

[27]  Helen E. Scharfman,et al.  The dentate gyrus : a comprehensive guide to structure, function, and clinical implications , 2007 .

[28]  C. A. Marsan,et al.  CORTICAL CELLULAR PHENOMENA IN EXPERIMENTAL EPILEPSY: INTERICTAL MANIFESTATIONS. , 1964, Experimental neurology.

[29]  Wilhelm Sommer,et al.  Erkrankung des Ammonshorns als aetiologisches Moment der Epilepsie , 1880, Archiv für Psychiatrie und Nervenkrankheiten.

[30]  A. Depaulis,et al.  Evolution of hippocampal epileptic activity during the development of hippocampal sclerosis in a mouse model of temporal lobe epilepsy , 2002, Neuroscience.

[31]  T. H. Brown,et al.  The synaptic nature of the paroxysmal depolarizing shift in hippocampal neurons , 1984, Annals of neurology.

[32]  F Edward Dudek,et al.  Unmasking recurrent excitation generated by mossy fiber sprouting in the epileptic dentate gyrus: an emergent property of a complex system. , 2007, Progress in brain research.

[33]  P. Brown,et al.  Creutzfeldt‐Jakob disease of long duration: Clinicopathological characteristics, transmissibility, and differential diagnosis , 1984, Annals of neurology.

[34]  J. Hughlingsjackson,et al.  ON A PARTICULAR VARIETY OF EPILEPSY (“INTELLECTUAL AURA”), ONE CASE WITH SYMPTOMS OF ORGANIC BRAIN DISEASE , 1888 .

[35]  D. Prince,et al.  Postnatal development of electrogenic sodium pump activity in rat hippocampal pyramidal neurons. , 1992, Brain research. Developmental brain research.

[36]  M. Cuttle,et al.  Mechanisms of neuronal hyperexcitability caused by partial inhibition of Na+-K+-ATPases in the rat CA1 hippocampal region. , 2002, Journal of neurophysiology.

[37]  F. A. Gibbs,et al.  Epilepsy: a paroxysmal cerebral dysrhythmia , 2002, Epilepsy & Behavior.

[38]  T. Grisar,et al.  Contribution of Na+,K+-ATPase to focal epilepsy: a brief review , 1992, Epilepsy Research.

[39]  R. Kuzniecky,et al.  Temporal lobe developmental malformations and epilepsy , 1998, Neurology.

[40]  D. Lewis,et al.  Losing Neurons: Selective Vulnerability and Mesial Temporal Sclerosis , 2005, Epilepsia.

[41]  I. Jensen,et al.  TEMPORAL LOBE EPILEPSY , 1976, Acta Neurochirurgica.

[42]  H. Jasper,et al.  EEG and cortical electrograms in patients with temporal lobe seizures. , 1951, A.M.A. archives of neurology and psychiatry.

[43]  J. Nadler,et al.  The Recurrent Mossy Fiber Pathway of the Epileptic Brain , 2003, Neurochemical Research.

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