Your browser doesn't support javascript.
loading
Laminar analysis of the slow wave activity in the somatosensory cortex of anesthetized rats.
Fiáth, Richárd; Kerekes, Bálint Péter; Wittner, Lucia; Tóth, Kinga; Beregszászi, Patrícia; Horváth, Domonkos; Ulbert, István.
Afiliação
  • Fiáth R; Institute of Cognitive Neuroscience and Psychology, Research Centre for Natural Sciences, Hungarian Academy of Sciences, Magyar tudósok körútja 2, Budapest, 1117, Hungary.
  • Kerekes BP; School of Ph.D. Studies, Semmelweis University, Budapest, Hungary.
  • Wittner L; Faculty of Information Technology and Bionics, Pázmány Péter Catholic University, Budapest, Hungary.
  • Tóth K; Faculty of Information Technology and Bionics, Pázmány Péter Catholic University, Budapest, Hungary.
  • Beregszászi P; Institute of Cognitive Neuroscience and Psychology, Research Centre for Natural Sciences, Hungarian Academy of Sciences, Magyar tudósok körútja 2, Budapest, 1117, Hungary.
  • Horváth D; Institute of Cognitive Neuroscience and Psychology, Research Centre for Natural Sciences, Hungarian Academy of Sciences, Magyar tudósok körútja 2, Budapest, 1117, Hungary.
  • Ulbert I; Faculty of Information Technology and Bionics, Pázmány Péter Catholic University, Budapest, Hungary.
Eur J Neurosci ; 44(3): 1935-51, 2016 08.
Article em En | MEDLINE | ID: mdl-27177594
ABSTRACT
Rhythmic slow waves characterize brain electrical activity during natural deep sleep and under anesthesia, reflecting the synchronous membrane potential fluctuations of neurons in the thalamocortical network. Strong evidence indicates that the neocortex plays an important role in the generation of slow wave activity (SWA), however, contributions of individual cortical layers to the SWA generation are still unclear. The anatomically correct laminar profiles of SWA were revealed under ketamine/xylazine anesthesia, with combined local field potential recordings, multiple-unit activity (MUA), current source density (CSD) and time-frequency analyses precisely co-registered with histology. The up-state related negative field potential wave showed the largest amplitude in layer IV, the CSD was largest in layers I and III, whereas MUA was maximal in layer V, suggesting spatially dissociated firing and synaptic/transmembrane processes in the rat somatosensory cortex. Up-state related firing could start in virtually any layers (III-VI) of the cortex, but were most frequently initiated in layer V. However, in a subset of experiments, layer IV was considerably active in initiating up-state related MUA even in the absence of somatosensory stimulation. Somatosensory stimulation further strengthened up-state initiation in layer IV. Our results confirm that cortical layer V firing may have a major contribution to the up-state generation of ketamine/xylazine-induced SWA, however, thalamic influence through the thalamorecipient layer IV can also play an initiating role, even in the absence of sensory stimulation.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Córtex Somatossensorial / Ondas Encefálicas Limite: Animals Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Córtex Somatossensorial / Ondas Encefálicas Limite: Animals Idioma: En Ano de publicação: 2016 Tipo de documento: Article