7 research outputs found

    Extent of single-neuron activity modulation by hippocampal interictal discharges predicts declarative memory disruption in humans

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    Memory deficits are common in epilepsy patients. In these patients, the interictal EEG commonly shows interictal epileptiform discharges (IEDs). While IEDs are associated with transient cognitive impairments, it remains poorly understood why this is. We investigated the effects of human (male and female) hippocampal IEDs on single-neuron activity during a memory task in patients with medically refractory epilepsy undergoing depth electrode monitoring. We quantified the effects of hippocampal IEDs on single-neuron activity and the impact of this modulation on subjectively declared memory strength. Across all recorded neurons, the activity of 50 of 728 neurons were significantly modulated by IEDs, with the strongest modulation in the medial temporal lobe (33 of 416) and in particular the right hippocampus (12 of 58). Putative inhibitory neurons, as identified by their extracellular signature, were more likely to be modulated by IEDs than putative excitatory neurons (19 of 157 vs 31 of 571). Behaviorally, the occurrence of hippocampal IEDs was accompanied by a disruption of recognition of familiar images only if they occurred up to 2 s before stimulus onset. In contrast, IEDs did not impair encoding or recognition of novel images, indicating high temporal and task specificity of the effects of IEDs. The degree of modulation of individual neurons by an IED correlated with the declared confidence of a retrieval trial, with higher firing rates indicative of reduced confidence. Together, these data link the transient modulation of individual neurons by IEDs to specific declarative memory deficits in specific cell types, thereby revealing a mechanism by which IEDs disrupt medial temporal lobe-dependent declarative memory retrieval processes

    A NWB-based dataset and processing pipeline of human single-neuron activity during a declarative memory task

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    A challenge for data sharing in systems neuroscience is the multitude of different data formats used. Neurodata Without Borders: Neurophysiology 2.0 (NWB:N) has emerged as a standardized data format for the storage of cellular-level data together with meta-data, stimulus information, and behavior. A key next step to facilitate NWB:N adoption is to provide easy to use processing pipelines to import/export data from/to NWB:N. Here, we present a NWB-formatted dataset of 1863 single neurons recorded from the medial temporal lobes of 59 human subjects undergoing intracranial monitoring while they performed a recognition memory task. We provide code to analyze and export/import stimuli, behavior, and electrophysiological recordings to/from NWB in both MATLAB and Python. The data files are NWB:N compliant, which affords interoperability between programming languages and operating systems. This combined data and code release is a case study for how to utilize NWB:N for human single-neuron recordings and enables easy re-use of this hard-to-obtain data for both teaching and research on the mechanisms of human memory

    Los archivalia de Arias Montano en el Museo Plantin-Moretus de Amberes

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    En el presente trabajo ofrecemos un recorrido por los documentos de Benito Arias Montano conservados en el Museo Plantin-Moretus de Amberes. De los riquísimos fondos de esta institución existen ya dos inventarios, uno de manuscritos y otro de archivos. Sin embargo, la descripción bibliográfica que estos ofrecen dista mucho de ser exhaustiva; más bien se queda en la superficie. En una comparación fácil con la arqueología, se puede decir que los primeros conservadores de dicho museo realizaron una primera prospección horizontal y a cada uno de los investigadores les toca excavar en dirección vertical la parcela que les interese. Los resultados de nuestra búsqueda, centrada en Arias Montano, pueden agruparse en cinco bloques: correspondencia, pedidos de libros, documentos comerciales, cuentas con la casa plantiniana y un apartado misceláneo que llamamos varia
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