Cortical Focus Drives Widespread Corticothalamic Networks during Spontaneous Absence Seizures in Rats

Absence seizures are the most pure form of generalized epilepsy. They are characterized in the electroencephalogram by widespread bilaterally synchronous spike-wave discharges (SWDs), which are the reflections of highly synchronized oscillations in thalamocortical networks. To reveal network mechanisms responsible for the initiation and generalization of the discharges, we studied the interrelationships between multisite cortical and thalamic field potentials recorded during spontaneous SWDs in the freely moving WAG/Rij rat, a genetic model of absence epilepsy. Nonlinear association analysis revealed a consistent cortical “focus” within the peri-oral region of the somatosensory cortex. The SWDs recorded at other cortical sites consistently lagged this focal site, with time delays that increased with electrode distance (corresponding to a mean propagation velocity of 1.4 m/sec). Intra-thalamic relationships were more complex and could not account for the observed cortical propagation pattern. Cortical and thalamic sites interacted bi-directionally, whereas the direction of this coupling could vary throughout one seizure. However, during the first 500 msec, the cortical focus was consistently found to lead the thalamus. These findings argue against the existence of one common subcortical pacemaker for the generation of generalized spike-wave discharges characteristic for absence seizures in the rat. Instead, the results suggest that a cortical focus is the dominant factor in initiating the paroxysmal oscillation within the corticothalamic loops, and that the large-scale synchronization is mediated by ways of an extremely fast intracortical spread of seizure activity. Analogous mechanisms may underlie the pathophysiology of human absence epilepsy.

[1]  H. Jasper,et al.  ELECTROENCEPHALOGRAPHIC CLASSIFICATION OF THE EPILEPSIES , 1941 .

[2]  D. Williams,et al.  A study of thalamic and cortical rhythms in petit mal. , 1953, Brain : a journal of neurology.

[3]  R.N.Dej.,et al.  Epilepsy and the Functional Anatomy of the Human Brain , 1954, Neurology.

[4]  H. Harlow,et al.  The History and Philosophy of Knowledge of the Brain and its Functions , 1960, Neurology.

[5]  [Pathophysiology and clinical aspects of petitmal. Toposcopic studies on the phenomenology of the spike wave pattern]. , 1962, Wiener Zeitschrift fur Nervenheilkunde und deren Grenzgebiete.

[6]  H Petsche,et al.  The significance of the cortex for the travelling phenomenon of brain waves. , 1968, Electroencephalography and clinical neurophysiology.

[7]  H Petsche,et al.  Influence of cortical incisions on synchronization pattern and travelling waves. , 1970, Electroencephalography and clinical neurophysiology.

[8]  C. Welker Microelectrode delineation of fine grain somatotopic organization of (SmI) cerebral neocortex in albino rat. , 1971, Brain research.

[9]  F. D. da Silva,et al.  Organization of thalamic and cortical alpha rhythms: spectra and coherences. , 1973, Electroencephalography and clinical neurophysiology.

[10]  W. Alvarez The Generalized Epilepsies: A Clinical Electroencephalographic Study. , 1974 .

[11]  F. H. Lopes da Silva,et al.  Relative contributions of intracortical and thalamo-cortical processes in the generation of alpha rhythms, revealed by partial coherence analysis. , 1980, Electroencephalography and clinical neurophysiology.

[12]  G. Micheletti,et al.  Spontaneous paroxysmal electroclinical patterns in rat: A model of generalized non-convulsive epilepsy , 1982, Neuroscience Letters.

[13]  J Gotman,et al.  An analysis of penicillin-induced generalized spike and wave discharges using simultaneous recordings of cortical and thalamic single neurons. , 1983, Journal of neurophysiology.

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

[15]  J. Chapin,et al.  Mapping the body representation in the SI cortex of anesthetized and awake rats , 1984, The Journal of comparative neurology.

[16]  L. Swanson The Rat Brain in Stereotaxic Coordinates, George Paxinos, Charles Watson (Eds.). Academic Press, San Diego, CA (1982), vii + 153, $35.00, ISBN: 0 125 47620 5 , 1984 .

[17]  A. Coenen,et al.  Two types of electrocortical paroxysms in an inbred strain of rats , 1986, Neuroscience Letters.

[18]  M. O'connor,et al.  Motor areas of the cerebral cortex , 1987 .

[19]  R. Llinás,et al.  The functional states of the thalamus and the associated neuronal interplay. , 1988, Physiological reviews.

[20]  George K. Kostopoulos,et al.  Thalamocortical Relationships in Generalized Epilepsy with Bilaterally Synchronous Spike-and-Wave Discharge , 1990 .

[21]  A. Coenen,et al.  Spike-wave discharges and sleep-wake states in rats with absence epilepsy , 1991, Epilepsy Research.

[22]  G. Buzsáki The thalamic clock: Emergent network properties , 1991, Neuroscience.

[23]  A. Coenen,et al.  Absence epilepsy and the level of vigilance in rats of the WAG/Rij strain , 1991, Neuroscience & Biobehavioral Reviews.

[24]  E. van Luijtelaar,et al.  Arousal, performance and absence seizures in rats. , 1991, Electroencephalography and clinical neurophysiology.

[25]  B. Connors,et al.  Intrinsic oscillations of neocortex generated by layer 5 pyramidal neurons. , 1991, Science.

[26]  A. Coenen,et al.  Genetic models of absence epilepsy, with emphasis on the WAG/Rij strain of rats , 1992, Epilepsy Research.

[27]  Jacques Duysens,et al.  Thalamic multiple-unit activity underlying spike-wave discharges in anesthetized rats , 1993, Brain Research.

[28]  M Steriade,et al.  Dynamic coupling among neocortical neurons during evoked and spontaneous spike-wave seizure activity. , 1994, Journal of neurophysiology.

[29]  D Contreras,et al.  Relations between cortical and thalamic cellular events during transition from sleep patterns to paroxysmal activity , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[30]  M. Nicolelis,et al.  Sensorimotor encoding by synchronous neural ensemble activity at multiple levels of the somatosensory system. , 1995, Science.

[31]  D. Contreras,et al.  Spindle oscillation in cats: the role of corticothalamic feedback in a thalamically generated rhythm. , 1996, The Journal of physiology.

[32]  J O Willoughby,et al.  Frontal cortex leads other brain structures in generalised spike-and-wave spindles and seizure spikes induced by picrotoxin. , 1996, Electroencephalography and clinical neurophysiology.

[33]  E. Niedermeyer,et al.  Primary (Idiopathic) Generalized Epilepsy and Underlying Mechanisms , 1996, Clinical EEG.

[34]  B. Connors,et al.  Two types of network oscillations in neocortex mediated by distinct glutamate receptor subtypes and neuronal populations. , 1996, Journal of neurophysiology.

[35]  T. Sejnowski,et al.  Control of Spatiotemporal Coherence of a Thalamic Oscillation by Corticothalamic Feedback , 1996, Science.

[36]  B W Connors,et al.  Spatiotemporal properties of short-term plasticity sensorimotor thalamocortical pathways of the rat , 1996, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[37]  G Buzsáki,et al.  Cellular–Synaptic Generation of Sleep Spindles, Spike-and-Wave Discharges, and Evoked Thalamocortical Responses in the Neocortex of the Rat , 1997, The Journal of Neuroscience.

[38]  D. McCormick,et al.  Sleep and arousal: thalamocortical mechanisms. , 1997, Annual review of neuroscience.

[39]  Cortical spreading depression suppresses spike wave discharges in the WAG/RIJ rat , 1997 .

[40]  C. Lombroso Consistent EEG Focalities Detected in Subjects with Primary Generalized Epilepsies Monitored for Two Decades , 1997, Epilepsia.

[41]  T Seidenbecher,et al.  Relations between cortical and thalamic cellular activities during absence seizures in rats , 1998, The European journal of neuroscience.

[42]  D. Pinault,et al.  Intracellular recordings in thalamic neurones during spontaneous spike and wave discharges in rats with absence epilepsy , 1998, The Journal of physiology.

[43]  D. Contreras,et al.  Spike-wave complexes and fast components of cortically generated seizures. I. Role of neocortex and thalamus. , 1998, Journal of neurophysiology.

[44]  M Steriade,et al.  Spike-wave complexes and fast components of cortically generated seizures. III. Synchronizing mechanisms. , 1998, Journal of neurophysiology.

[45]  L. Danober,et al.  Pathophysiological mechanisms of genetic absence epilepsy in the rat , 1998, Progress in Neurobiology.

[46]  M. Curtis,et al.  The role of the thalamus in vigilance and epileptogenic mechanisms , 2000, Clinical Neurophysiology.

[47]  A. Coenen,et al.  Electrophysiological and pharmacological characteristics of two types of spike-wave discharges in WAG/Rij rats , 2001, Brain Research.

[48]  J. Bellanger,et al.  Interpretation of interdependencies in epileptic signals using a macroscopic physiological model of the EEG , 2001, Clinical Neurophysiology.