Disruption of TLE epileptiform activity retarded the seizure and reduced pathological HFOs.

CA3 Pathological high-frequency oscillations Pharmaco-genetic firing rate temporal lobe epilepsy

Journal

Brain research bulletin
ISSN: 1873-2747
Titre abrégé: Brain Res Bull
Pays: United States
ID NLM: 7605818

Informations de publication

Date de publication:
04 Jan 2024
Historique:
received: 31 10 2023
revised: 17 12 2023
accepted: 01 01 2024
medline: 7 1 2024
pubmed: 7 1 2024
entrez: 6 1 2024
Statut: aheadofprint

Résumé

In temporal lobe epilepsy (TLE), the epileptogenic zones, such as the temporal lobe structure, could generate pathological high-frequency oscillations (pHFOs, 250-500Hz) before the ictal period. These pHFOs have also been observed during the process of seizures in both TLE patients and animals, exhibiting a critical role as promising biomarkers for TLE seizures. TLE seizures could be modulated via regulating the neural excitability in epileptogenic zones, for that TLE is primarily associated with the excitation-inhibition imbalance. However, whether these kinds of modulations could also impact the pHFOs characteristics during TLE seizures is still unclear. For this purpose, we pharmaco-genetically inhibited the principal cells (PCs) in the mouse CA3 region and tracked the difference in the behavioral and electrophysiological features during LiCl-pilocarpine-induced TLE seizure between the hM4Di+CNO (experimental) mice and mCherry+CNO (control) mice. Delayed latency, decreased averaged duration, and reduced counts of the generalized seizure were observed in the experimental mice. Besides, the electrophysiological characteristics, such as the firing rate of PCs and the count of pHFO, exhibited significant decline in the CA3 and CA1 regions. During TLE seizure, there existed strong phase-coupling between pHFO and PCs spike timing in the control mice, while it was abolished in the experimental mice. In addition, we also found that the counts of pHFO were significantly associated with the behavioral features, indicating the close relationships within them. Collectively, our findings suggested that alterations in pHFO and the retardation of seizures may be attributed to disruptions in neuronal excitability, and the variations of electrophysiological features were related to seizure severity during TLE seizures. These results provide valuable insights into the role of pHFOs in TLE and shed light on the underlying mechanisms involved.

Identifiants

pubmed: 38184151
pii: S0361-9230(24)00002-9
doi: 10.1016/j.brainresbull.2024.110869
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

110869

Informations de copyright

Copyright © 2024 The Authors. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Fengru Guo (F)

Department of Neurosurgery, Sichuan Provincial People's Hospital, MOE Key Lab for Neuroinformation, University of Electronic Science and Technology of China, Chengdu, 611731, China. Electronic address: 201811140111@std.uestc.edu.cn.

Airui Li (A)

Department of Neurosurgery, Sichuan Provincial People's Hospital, MOE Key Lab for Neuroinformation, University of Electronic Science and Technology of China, Chengdu, 611731, China. Electronic address: 17340021713@163.com.

Qinjun Liu (Q)

Department of Neurosurgery, Sichuan Provincial People's Hospital, MOE Key Lab for Neuroinformation, University of Electronic Science and Technology of China, Chengdu, 611731, China. Electronic address: lliuqinjun@163.com.

Daqing Guo (D)

Department of Neurosurgery, Sichuan Provincial People's Hospital, MOE Key Lab for Neuroinformation, University of Electronic Science and Technology of China, Chengdu, 611731, China. Electronic address: dqguo@uestc.edu.cn.

Ke Chen (K)

Department of Neurosurgery, Sichuan Provincial People's Hospital, MOE Key Lab for Neuroinformation, University of Electronic Science and Technology of China, Chengdu, 611731, China. Electronic address: chenke0703@uestc.edu.cn.

Dezhong Yao (D)

Department of Neurosurgery, Sichuan Provincial People's Hospital, MOE Key Lab for Neuroinformation, University of Electronic Science and Technology of China, Chengdu, 611731, China. Electronic address: dyao@uestc.edu.cn.

Yan Cui (Y)

Department of Neurosurgery, Sichuan Provincial People's Hospital, MOE Key Lab for Neuroinformation, University of Electronic Science and Technology of China, Chengdu, 611731, China. Electronic address: cuiyanlance@163.com.

Yang Xia (Y)

Department of Neurosurgery, Sichuan Provincial People's Hospital, MOE Key Lab for Neuroinformation, University of Electronic Science and Technology of China, Chengdu, 611731, China. Electronic address: xiayang2930@163.com.

Classifications MeSH