<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Curot J</submitter><funding>European Union’s Seventh Framework Programme</funding><funding>International Development Research Centre, Canada</funding><funding>Fondation Française pour la Recherche sur l'Epilepsie</funding><funding>Canada-Israel Health Research Initiative</funding><funding>Canada Brain Research Fund</funding><funding>Canadian Institutes of Health Research</funding><funding>CIHR</funding><funding>Fondation Française pour la Recherche sur l’Epilepsie</funding><funding>European Research Council</funding><funding>Azrieli Foundation</funding><funding>European Union's Seventh Framework Programme</funding><funding>Israel Science Foundation</funding><funding>NSERC Discovery</funding><funding>CIHR Project</funding><pagination>561-575</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9924905</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>146(2)</volume><pubmed_abstract>Understanding the neuronal basis of epileptic activity is a major challenge in neurology. Cellular integration into larger scale networks is all the more challenging. In the local field potential, interictal epileptic discharges can be associated with fast ripples (200-600 Hz), which are a promising marker of the epileptogenic zone. Yet, how neuronal populations in the epileptogenic zone and in healthy tissue are affected by fast ripples remain unclear. Here, we used a novel 'hybrid' macro-micro depth electrode in nine drug-resistant epileptic patients, combining classic depth recording of local field potentials (macro-contacts) and two or three tetrodes (four micro-wires bundled together) enabling up to 15 neurons in local circuits to be simultaneously recorded. We characterized neuronal </pubmed_abstract><journal>Brain : a journal of neurology</journal><pubmed_title>Local neuronal excitation and global inhibition during epileptic fast ripples in humans.</pubmed_title><pmcid>PMC9924905</pmcid><funding_grant_id>FP/2007-2013</funding_grant_id><funding_grant_id>RGPIN-2018-04600</funding_grant_id><funding_grant_id>108877-001</funding_grant_id><funding_grant_id>155957</funding_grant_id><funding_grant_id>323711</funding_grant_id><pubmed_authors>Lotterie JA</pubmed_authors><pubmed_authors>Despouy E</pubmed_authors><pubmed_authors>Sol JC</pubmed_authors><pubmed_authors>Barbeau E</pubmed_authors><pubmed_authors>Curot J</pubmed_authors><pubmed_authors>Valton L</pubmed_authors><pubmed_authors>Denuelle M</pubmed_authors><pubmed_authors>Peyrache A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Local neuronal excitation and global inhibition during epileptic fast ripples in humans.</name><description>Understanding the neuronal basis of epileptic activity is a major challenge in neurology. Cellular integration into larger scale networks is all the more challenging. In the local field potential, interictal epileptic discharges can be associated with fast ripples (200-600 Hz), which are a promising marker of the epileptogenic zone. Yet, how neuronal populations in the epileptogenic zone and in healthy tissue are affected by fast ripples remain unclear. Here, we used a novel 'hybrid' macro-micro depth electrode in nine drug-resistant epileptic patients, combining classic depth recording of local field potentials (macro-contacts) and two or three tetrodes (four micro-wires bundled together) enabling up to 15 neurons in local circuits to be simultaneously recorded. We characterized neuronal </description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Feb</publication><modification>2025-04-18T21:29:35.724Z</modification><creation>2025-04-07T09:20:58.809Z</creation></dates><accession>S-EPMC9924905</accession><cross_references><pubmed>36093747</pubmed><doi>10.1093/brain/awac319</doi></cross_references></HashMap>