Literature DB >> 15144857

In vivo laminar electrophysiology co-registered with histology in the hippocampus of patients with temporal lobe epilepsy.

István Ulbert1, Zsófia Maglóczky, Loránd Eross, Sándor Czirják, János Vajda, László Bognár, Szabolcs Tóth, Zerind Szabó, Péter Halász, Dániel Fabó, Eric Halgren, Tamás F Freund, George Karmos.   

Abstract

Laminar multiple microelectrodes have been developed to sample cortical and hippocampal activity in animals. If these measurements are adequately co-registered with the anatomy of the region, they can yield important information about its function and structure. In vivo laminar electrophysiological recordings from the human epileptic hippocampus are rare. However, histological and immunohistochemical analyses are widely used to determine the structural changes associated with temporal lobe epilepsy (TLE). Here we present data obtained by a combined approach: intraoperative recording of laminar field potentials, single and multiple unit activity under anesthesia, accompanied by histology and immunohistochemistry from the same hippocampal region of epileptic patients undergoing temporal lobectomy for drug-resistant TLE. The stability of the electrophysiology and the accuracy of its co-registration with histology were tested successfully. We have found large field potential spikes associated with bursting single units in CA1. Intracortical and subdural strip recordings from the lateral temporal cortex showed similar field potential activation patterns. A prominent oscillatory activity was present in the dentate gyrus with highly localized field potential gradient and multiple unit activity. This pattern could be used as a landmark defining the position of the electrode in the hippocampus. Our findings indicate that some aspects of the local and network epileptiform activity in the hippocampal formation are likely preserved under anesthesia. Electrophysiological identification of the functional state of the hippocampus together with its local structural correlates could further enhance our understanding of this disease.

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Year:  2004        PMID: 15144857     DOI: 10.1016/j.expneurol.2003.12.003

Source DB:  PubMed          Journal:  Exp Neurol        ISSN: 0014-4886            Impact factor:   5.330


  14 in total

1.  Combined two-photon imaging, electrophysiological, and anatomical investigation of the human neocortex in vitro.

Authors:  Bálint Péter Kerekes; Kinga Tóth; Attila Kaszás; Balázs Chiovini; Zoltán Szadai; Gergely Szalay; Dénes Pálfi; Attila Bagó; Klaudia Spitzer; Balázs Rózsa; István Ulbert; Lucia Wittner
Journal:  Neurophotonics       Date:  2014-09-11       Impact factor: 3.593

Review 2.  Recording and analysis techniques for high-frequency oscillations.

Authors:  G A Worrell; K Jerbi; K Kobayashi; J M Lina; R Zelmann; M Le Van Quyen
Journal:  Prog Neurobiol       Date:  2012-03-07       Impact factor: 11.685

3.  Hyperexcitability of the network contributes to synchronization processes in the human epileptic neocortex.

Authors:  Kinga Tóth; Katharina T Hofer; Ágnes Kandrács; László Entz; Attila Bagó; Loránd Erőss; Zsófia Jordán; Gábor Nagy; András Sólyom; Dániel Fabó; István Ulbert; Lucia Wittner
Journal:  J Physiol       Date:  2017-12-28       Impact factor: 5.182

4.  First-pass selectivity for semantic categories in human anteroventral temporal lobe.

Authors:  Alexander M Chan; Janet M Baker; Emad Eskandar; Donald Schomer; Istvan Ulbert; Ksenija Marinkovic; Sydney S Cash; Eric Halgren
Journal:  J Neurosci       Date:  2011-12-07       Impact factor: 6.167

5.  Laminar analysis of slow wave activity in humans.

Authors:  Richárd Csercsa; Balázs Dombovári; Dániel Fabó; Lucia Wittner; Loránd Eross; László Entz; András Sólyom; György Rásonyi; Anna Szucs; Anna Kelemen; Rita Jakus; Vera Juhos; László Grand; Andor Magony; Péter Halász; Tamás F Freund; Zsófia Maglóczky; Sydney S Cash; László Papp; György Karmos; Eric Halgren; István Ulbert
Journal:  Brain       Date:  2010-07-23       Impact factor: 13.501

6.  Role of A-type potassium currents in excitability, network synchronicity, and epilepsy.

Authors:  Erik Fransén; Jenny Tigerholm
Journal:  Hippocampus       Date:  2010-07       Impact factor: 3.899

7.  Microphysiology of epileptiform activity in human neocortex.

Authors:  Catherine A Schevon; Sau K Ng; Joshua Cappell; Robert R Goodman; Guy McKhann; Allen Waziri; Almut Branner; Alexandre Sosunov; Charles E Schroeder; Ronald G Emerson
Journal:  J Clin Neurophysiol       Date:  2008-12       Impact factor: 2.177

8.  Laminar distribution of electrically evoked hippocampal short latency ripple activity highlights the importance of the subiculum in vivo in human epilepsy, an intraoperative study.

Authors:  Emília Tóth; Virág Bokodi; Zoltán Somogyvári; Zsófia Maglóczky; Lucia Wittner; István Ulbert; Loránd Erőss; Dániel Fabó
Journal:  Epilepsy Res       Date:  2020-11-24       Impact factor: 3.045

9.  Spatial characterization of interictal high frequency oscillations in epileptic neocortex.

Authors:  Catherine A Schevon; A J Trevelyan; C E Schroeder; R R Goodman; G McKhann; R G Emerson
Journal:  Brain       Date:  2009-09-10       Impact factor: 13.501

10.  Utilization of independent component analysis for accurate pathological ripple detection in intracranial EEG recordings recorded extra- and intra-operatively.

Authors:  Shoichi Shimamoto; Zachary J Waldman; Iren Orosz; Inkyung Song; Anatol Bragin; Itzhak Fried; Jerome Engel; Richard Staba; Ashwini Sharan; Chengyuan Wu; Michael R Sperling; Shennan A Weiss
Journal:  Clin Neurophysiol       Date:  2017-10-25       Impact factor: 3.708

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