| Literature DB >> 26157969 |
Bálint Péter Kerekes1, Kinga Tóth2, Attila Kaszás3, Balázs Chiovini3, Zoltán Szadai3, Gergely Szalay4, Dénes Pálfi3, Attila Bagó5, Klaudia Spitzer4, Balázs Rózsa3, István Ulbert1, Lucia Wittner6.
Abstract
Spontaneous synchronous population activity (SPA) can be detected by electrophysiological methods in cortical slices of epileptic patients, maintained in a physiological medium in vitro. In order to gain additional spatial information about the network mechanisms involved in the SPA generation, we combined electrophysiological studies with two-photon imaging. Neocortical slices prepared from postoperative tissue of epileptic and tumor patients were maintained in a dual perfusion chamber in a physiological incubation medium. SPA was recorded with a 24-channel extracellular linear microelectrode covering all neocortical layers. After identifying the electrophysiologically active regions of the slice, bolus loading of neuronal and glial markers was applied on the tissue. SPA-related [Formula: see text] transients were detected in a large population of neighboring neurons with two-photon microscopy, simultaneous with extracellular SPA and intracellular whole-cell patch-clamp recordings. The intracellularly recorded cells were filled for subsequent anatomy. The cells were reconstructed in three dimensions and examined with light- and transmission electron microscopy. Combining high spatial resolution two-photon [Formula: see text] imaging techniques and high temporal resolution extra- and intracellular electrophysiology with cellular anatomy may permit a deeper understanding of the structural and functional properties of the human neocortex.Entities:
Keywords: epilepsy; glutamate uncaging; human; neocortex; synchrony; two-photon imaging
Year: 2014 PMID: 26157969 PMCID: PMC4478968 DOI: 10.1117/1.NPh.1.1.011013
Source DB: PubMed Journal: Neurophotonics ISSN: 2329-423X Impact factor: 3.593