Enhanced Synaptic Connectivity in the Dentate Gyrus during Epileptiform Activity: Network Simulation

Structural rearrangement of the dentate gyrus has been described as the underlying cause of many types of epilepsies, particularly temporal lobe epilepsy. It is said to occur when aberrant connections are established in the damaged hippocampus, as described in human epilepsy and experimental models. Computer modelling of the dentate gyrus circuitry and the corresponding structural changes has been used to understand how abnormal mossy fibre sprouting can subserve seizure generation observed in experimental models when epileptogenesis is induced by status epilepticus. The model follows the McCulloch-Pitts formalism including the representation of the nonsynaptic mechanisms. The neuronal network comprised granule cells, mossy cells, and interneurons. The compensation theory and the Hebbian and anti-Hebbian rules were used to describe the structural rearrangement including the effects of the nonsynaptic mechanisms on the neuronal activity. The simulations were based on neuroanatomic data and on the connectivity pattern between the cells represented. The results suggest that there is a joint action of the compensation theory and Hebbian rules during the inflammatory process that accompanies the status epilepticus. The structural rearrangement simulated for the dentate gyrus circuitry promotes speculation about the formation of the abnormal mossy fiber sprouting and its role in epileptic seizures.

[1]  F. Dudek,et al.  Synchronous neural afterdischarges in rat hippocampal slices without active chemical synapses. , 1982, Science.

[2]  P. Rutecki,et al.  Spontaneous Seizures and Loss of Axo-Axonic and Axo-Somatic Inhibition Induced by Repeated Brief Seizures in Kindled Rats , 2003, The Journal of Neuroscience.

[3]  J. Lisman,et al.  A mechanism for the Hebb and the anti-Hebb processes underlying learning and memory. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[4]  Antônio-Carlos G. Almeida,et al.  Biophysical Aspects of the Nonsynaptic Epileptiform Activity , 2011 .

[5]  G. Flint,et al.  Seizures and epilepsy. , 1988, British journal of neurosurgery.

[6]  Orfa Yineth Galvis-Alonso,et al.  Plasticidade neuronal associada à epilepsia do lobo temporal mesial: insights a partir de estudos em humanos e em modelos animais , 2006 .

[7]  G. Wagner,et al.  ON THE PROPERTIES OF RANDOMLY CONNECTED McCULLOCH-PITTS NETWORKS: DIFFERENCES BETWEEN INPUT-CONSTANT AND INPUT-VARIANT NETWORKS , 1984 .

[8]  J. L. Stringer,et al.  Sodium pump activity, not glial spatial buffering, clears potassium after epileptiform activity induced in the dentate gyrus. , 2000, Journal of neurophysiology.

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

[10]  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.

[11]  G. Wagner,et al.  Self-stabilization of neuronal networks. I. The compensation algorithm for synaptogenesis. , 1986, Biological cybernetics.

[12]  M. Danhof,et al.  Quantitative EEG analysis: a biomarker for epileptogenesis , 2008 .

[13]  I E Dammasch,et al.  Self-stabilization of neuronal networks , 1988, Biological Cybernetics.

[14]  R. Morgan,et al.  Nonrandom connectivity of the epileptic dentate gyrus predicts a major role for neuronal hubs in seizures , 2008, Proceedings of the National Academy of Sciences.

[15]  G. Wagner,et al.  Self-Organization in Synaptogenesis: Interaction Between the Formation of Excitatory and Inhibitory Synapses , 1983 .

[16]  Andrea T. U. Schaefers,et al.  Synaptic Remodeling in the Dentate Gyrus, CA3, CA1, Subiculum, and Entorhinal Cortex of Mice: Effects of Deprived Rearing and Voluntary Running , 2010, Neural plasticity.

[17]  K. Svoboda,et al.  Long-term in vivo imaging of experience-dependent synaptic plasticity in adult cortex , 2002, Nature.

[18]  William W. Lytton,et al.  Computer models of hippocampal circuit changes of the kindling model of epilepsy , 1998, Artif. Intell. Medicine.

[19]  Hemal R. Pathak,et al.  Disrupted Dentate Granule Cell Chloride Regulation Enhances Synaptic Excitability during Development of Temporal Lobe Epilepsy , 2007, The Journal of Neuroscience.

[20]  Michael Frotscher,et al.  Synapses formed by normal and abnormal hippocampal mossy fibers , 2006, Cell and Tissue Research.

[21]  J. Nadler,et al.  Recurrent mossy fiber pathway in rat dentate gyrus: synaptic currents evoked in presence and absence of seizure-induced growth. , 1999, Journal of neurophysiology.

[22]  P. Buckmaster,et al.  Axon Sprouting in a Model of Temporal Lobe Epilepsy Creates a Predominantly Excitatory Feedback Circuit , 2002, The Journal of Neuroscience.

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

[24]  K. Svoboda,et al.  Cell Type-Specific Structural Plasticity of Axonal Branches and Boutons in the Adult Neocortex , 2006, Neuron.

[25]  R. Racine,et al.  Long-term potentiation trains induce mossy fiber sprouting , 1997, Brain Research.

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

[27]  Ivan Soltesz,et al.  Role of mossy fiber sprouting and mossy cell loss in hyperexcitability: a network model of the dentate gyrus incorporating cell types and axonal topography. , 2005, Journal of neurophysiology.

[28]  H. Haas,et al.  Synchronized bursting of CA1 hippocampal pyramidal cells in the absence of synaptic transmission , 1982, Nature.

[29]  J. E. Franck,et al.  Physiologic and Morphologic Characteristics of Granule Cell Circuitry in Human Epileptic Hippocampus , 1995, Epilepsia.

[30]  L. Tsimring,et al.  Topological determinants of epileptogenesis in large-scale structural and functional models of the dentate gyrus derived from experimental data. , 2007, Journal of neurophysiology.

[31]  W S McCulloch,et al.  A logical calculus of the ideas immanent in nervous activity , 1990, The Philosophy of Artificial Intelligence.

[32]  L J Cromme,et al.  Compensation type algorithms for neural nets: stability and convergence , 1989, Journal of mathematical biology.

[33]  F. Scorza,et al.  Mechanistic hypotheses for nonsynaptic epileptiform activity induction and its transition from the interictal to ictal state—Computational simulation , 2008, Epilepsia.

[34]  R. Miles,et al.  Perturbed Chloride Homeostasis and GABAergic Signaling in Human Temporal Lobe Epilepsy , 2007, The Journal of Neuroscience.

[35]  Markus Butz,et al.  A theoretical network model to analyse neurogenesis and synaptogenesis in the dentate gyrus , 2006, Neural Networks.

[36]  W. H. Jordan,et al.  Mesial Temporal Lobe Epilepsy: Pathogenesis, Induced Rodent Models and Lesions , 2007, Toxicologic pathology.

[37]  A. Galanopoulou,et al.  Altered GABA Signaling in Early Life Epilepsies , 2011, Neural plasticity.

[38]  W. Lytton Computer modelling of epilepsy , 2008, Nature Reviews Neuroscience.

[39]  P. Buckmaster,et al.  Rapamycin Suppresses Mossy Fiber Sprouting But Not Seizure Frequency in a Mouse Model of Temporal Lobe Epilepsy , 2011, The Journal of Neuroscience.

[40]  M. Frotscher,et al.  Granule cell hyperexcitability in the early post‐traumatic rat dentate gyrus: the ‘irritable mossy cell’ hypothesis , 2000, The Journal of physiology.

[41]  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.