The Direct Relationship between Inhibitory Currents and Local Field Potentials

The frequency profiles of various extracellular field oscillations are known to reflect functional brain states, yet we lack detailed explanations of how these brain oscillations arise. Of particular clinical relevance are the high-frequency oscillations (HFOs) associated with interictal events and the onset of seizures. These time periods are also when pyramidal firing appears to be vetoed by high-frequency volleys of inhibitory synaptic currents, thereby providing an inhibitory restraint that opposes epileptiform spread (Trevelyan et al., 2006, 2007). The pattern and timing of this inhibitory volley is suggestive of a causal relationship between the restraint and HFOs. I show that at these times, isolated inhibitory currents from single pyramidal cells have a similarity to the extracellular signal that significantly exceeds chance. The ability to extrapolate from discrete currents in single cells to the extracellular signal arises because these inhibitory currents are synchronized in local populations of pyramidal cells. The visibility of these inhibitory currents in the field recordings is greatest when local pyramidal activity is suppressed: the correlation between the inhibitory currents and the field signal becomes worse when local activity increases, suggestive of a switch from one source of HFO to another as the restraint starts to fail. This association suggests that a significant component of HFOs reflects the last act of defiance in the face of an advancing ictal event.

[1]  E. D. Adrian,et al.  THE ORIGIN OF THE BERGER RHYTHM , 1935 .

[2]  B. Katz,et al.  Spontaneous subthreshold activity at motor nerve endings , 1952, The Journal of physiology.

[3]  D. Prince,et al.  Control mechanisms in cortical epileptogenic foci. "Surround" inhibition. , 1967, Archives of neurology.

[4]  P. Young,et al.  Time series analysis, forecasting and control , 1972, IEEE Transactions on Automatic Control.

[5]  C. Nicholson Electric current flow in excitable cells J. J. B. Jack, D. Noble &R. W. Tsien Clarendon Press, Oxford (1975). 502 pp., £18.00 , 1976, Neuroscience.

[6]  G. Jenkins,et al.  Time series analysis, forecasting and control , 1971 .

[7]  B H Gähwiler,et al.  Activity-dependent disinhibition. II. Effects of extracellular potassium, furosemide, and membrane potential on ECl- in hippocampal CA3 neurons. , 1989, Journal of neurophysiology.

[8]  B. Gähwiler,et al.  Activity-dependent disinhibition. I. Repetitive stimulation reduces IPSP driving force and conductance in the hippocampus in vitro. , 1989, Journal of neurophysiology.

[9]  F. Krasne,et al.  Evidence for a computational distinction between proximal and distal neuronal inhibition. , 1992, Science.

[10]  G. Buzsáki,et al.  High-frequency network oscillation in the hippocampus. , 1992, Science.

[11]  M. Deschenes,et al.  Low- and high-frequency membrane potential oscillations during theta activity in CA1 and CA3 pyramidal neurons of the rat hippocampus under ketamine-xylazine anesthesia. , 1993, Journal of neurophysiology.

[12]  K. Staley,et al.  Ionic mechanisms of neuronal excitation by inhibitory GABAA receptors , 1995, Science.

[13]  G. Buzsáki,et al.  Sharp wave-associated high-frequency oscillation (200 Hz) in the intact hippocampus: network and intracellular mechanisms , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[14]  G. Buzsáki,et al.  Gamma (40-100 Hz) oscillation in the hippocampus of the behaving rat , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[15]  K. Micheva,et al.  Postnatal Development of GABA Neurons in the Rat Somatosensory Barrel Cortex: A Quantitative Study , 1995, The European journal of neuroscience.

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

[17]  K. Micheva,et al.  Quantitative aspects of synaptogenesis in the rat barrel field cortex with special reference to GABA circuitry , 1996, The Journal of comparative neurology.

[18]  G. Buzsáki,et al.  Interneurons of the hippocampus , 1998, Hippocampus.

[19]  T. Freund,et al.  Differences between Somatic and Dendritic Inhibition in the Hippocampus , 1996, Neuron.

[20]  E G Jones,et al.  Inhibitory synaptogenesis in mouse somatosensory cortex. , 1997, Cerebral cortex.

[21]  R. Traub,et al.  Electrical coupling underlies high-frequency oscillations in the hippocampus in vitro , 1998, Nature.

[22]  Charles L. Wilson,et al.  Hippocampal and Entorhinal Cortex High‐Frequency Oscillations (100–500 Hz) in Human Epileptic Brain and in Kainic Acid‐Treated Rats with Chronic Seizures , 1999, Epilepsia.

[23]  S. Hestrin,et al.  A network of fast-spiking cells in the neocortex connected by electrical synapses , 1999, Nature.

[24]  Charles L. Wilson,et al.  High‐frequency oscillations in human brain , 1999, Hippocampus.

[25]  B. Connors,et al.  Two networks of electrically coupled inhibitory neurons in neocortex , 1999, Nature.

[26]  Peter Somogyi,et al.  Cell surface domain specific postsynaptic currents evoked by identified GABAergic neurones in rat hippocampus in vitro , 2000, The Journal of physiology.

[27]  P. Jonas,et al.  Efficacy and Stability of Quantal GABA Release at a Hippocampal Interneuron–Principal Neuron Synapse , 2000, The Journal of Neuroscience.

[28]  Roger D. Traub,et al.  A Model of High-Frequency Ripples in the Hippocampus Based on Synaptic Coupling Plus Axon–Axon Gap Junctions between Pyramidal Neurons , 2000, The Journal of Neuroscience.

[29]  H. Parri,et al.  Spontaneous astrocytic Ca2+ oscillations in situ drive NMDAR-mediated neuronal excitation , 2001, Nature Neuroscience.

[30]  J. Haueisen,et al.  Multiplicity in the high-frequency signals during the short-latency somatosensory evoked cortical activity in humans , 2001, Clinical Neurophysiology.

[31]  Y. Kawaguchi,et al.  Distinct Firing Patterns of Neuronal Subtypes in Cortical Synchronized Activities , 2001, The Journal of Neuroscience.

[32]  Fiona E. N. LeBeau,et al.  A Possible Role for Gap Junctions in Generation of Very Fast EEG Oscillations Preceding the Onset of, and Perhaps Initiating, Seizures , 2001 .

[33]  M. Steriade,et al.  Focal synchronization of ripples (80-200 Hz) in neocortex and their neuronal correlates. , 2001, Journal of neurophysiology.

[34]  Helen J. Cross,et al.  A Possible Role for Gap Junctions in Generation of Very Fast EEG Oscillations Preceding the Onset of, and Perhaps Initiating, Seizures , 2001, Epilepsia.

[35]  Itzhak Fried,et al.  Interictal high‐frequency oscillations (80–500Hz) in the human epileptic brain: Entorhinal cortex , 2002, Annals of neurology.

[36]  M. Steriade,et al.  The role of chloride-dependent inhibition and the activity of fast-spiking neurons during cortical spike–wave electrographic seizures , 2002, Neuroscience.

[37]  G. Buzsáki Theta Oscillations in the Hippocampus , 2002, Neuron.

[38]  Charles L. Wilson,et al.  Quantitative analysis of high-frequency oscillations (80-500 Hz) recorded in human epileptic hippocampus and entorhinal cortex. , 2002, Journal of neurophysiology.

[39]  S. Schiff,et al.  Decreased Neuronal Synchronization during Experimental Seizures , 2002, The Journal of Neuroscience.

[40]  M. Steriade,et al.  Neocortical very fast oscillations (ripples, 80-200 Hz) during seizures: intracellular correlates. , 2003, Journal of neurophysiology.

[41]  M. Steriade Neuronal Substrates of Sleep and Epilepsy , 2003 .

[42]  P. Somogyi,et al.  Brain-state- and cell-type-specific firing of hippocampal interneurons in vivo , 2003, Nature.

[43]  Miles A Whittington,et al.  Interneuron Diversity series: Inhibitory interneurons and network oscillations in vitro , 2003, Trends in Neurosciences.

[44]  D. Labiner,et al.  Neuronal Substrates of Sleep and Epilepsy , 2004 .

[45]  D. McCormick,et al.  Inhibitory Postsynaptic Potentials Carry Synchronized Frequency Information in Active Cortical Networks , 2005, Neuron.

[46]  Andrew J Trevelyan,et al.  Does inhibition balance excitation in neocortex? , 2005, Progress in biophysics and molecular biology.

[47]  H. Berger Über das Elektrenkephalogramm des Menschen , 1929, Archiv für Psychiatrie und Nervenkrankheiten.

[48]  Brendon O. Watson,et al.  Modular Propagation of Epileptiform Activity: Evidence for an Inhibitory Veto in Neocortex , 2006, The Journal of Neuroscience.

[49]  Guglielmo Foffani,et al.  Reduced Spike-Timing Reliability Correlates with the Emergence of Fast Ripples in the Rat Epileptic Hippocampus , 2007, Neuron.

[50]  R. Yuste,et al.  Feedforward Inhibition Contributes to the Control of Epileptiform Propagation Speed , 2007, The Journal of Neuroscience.

[51]  D. Kleinfeld,et al.  Is there a common origin to surround-inhibition as seen through electrical activity versus hemodynamic changes? Focus on "Duration-dependent response in SI to vibrotactile stimulation in squirrel monkey". , 2007, Journal of neurophysiology.

[52]  K. Staley Neurons Skip a Beat during Fast Ripples , 2007, Neuron.

[53]  A. Schulze-Bonhage,et al.  Seizure Prediction in Epilepsy , 2008 .

[54]  B. Schelter Seizure Prediction in Epilepsy: From Basic Mechanisms to Clinical Applications , 2008 .

[55]  P. Jonas,et al.  Postnatal Differentiation of Basket Cells from Slow to Fast Signaling Devices , 2008, The Journal of Neuroscience.

[56]  A. Pérez-Villalba Rhythms of the Brain, G. Buzsáki. Oxford University Press, Madison Avenue, New York (2006), Price: GB £42.00, p. 448, ISBN: 0-19-530106-4 , 2008 .