Focal lesions induce large-scale percolation of sleep-like intracerebral activity in awake humans.
Bistability
Effective connectivity
Intracranial recording
Radio-frequency thermo-coagulation
Stroke
Journal
NeuroImage
ISSN: 1095-9572
Titre abrégé: Neuroimage
Pays: United States
ID NLM: 9215515
Informations de publication
Date de publication:
01 07 2021
01 07 2021
Historique:
received:
06
11
2020
revised:
15
02
2021
accepted:
08
03
2021
pubmed:
28
3
2021
medline:
14
10
2021
entrez:
27
3
2021
Statut:
ppublish
Résumé
Focal cortical lesions are known to result in large-scale functional alterations involving distant areas; however, little is known about the electrophysiological mechanisms underlying these network effects. Here, we addressed this issue by analysing the short and long distance intracranial effects of controlled structural lesions in humans. The changes in Stereo-Electroencephalographic (SEEG) activity after Radiofrequency-Thermocoagulation (RFTC) recorded in 21 epileptic subjects were assessed with respect to baseline resting wakefulness and sleep activity. In addition, Cortico-Cortical Evoked Potentials (CCEPs) recorded before the lesion were employed to interpret these changes with respect to individual long-range connectivity patterns. We found that small structural ablations lead to the generation and large-scale propagation of sleep-like slow waves within the awake brain. These slow waves match those recorded in the same subjects during sleep, are prevalent in perilesional areas, but can percolate up to distances of 60 mm through specific long-range connections, as predicted by CCEPs. Given the known impact of slow waves on information processing and cortical plasticity, demonstrating their intrusion and percolation within the awake brain add key elements to our understanding of network dysfunction after cortical injuries.
Identifiants
pubmed: 33771696
pii: S1053-8119(21)00241-X
doi: 10.1016/j.neuroimage.2021.117964
pii:
doi:
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
117964Informations de copyright
Copyright © 2021 The Author(s). Published by Elsevier Inc. All rights reserved.