Seizures and sleep in the thalamus: Focal limbic seizures show divergent activity patterns in different thalamic nuclei

  • Li Feng
  • , Joshua E. Motelow
  • , Chanthia Ma
  • , William Biche
  • , Cian McCafferty
  • , Nicholas Smith
  • , Mengran Liu
  • , Qiong Zhan
  • , Ruonan Jia
  • , Bo Xiao
  • , Alvaro Duque
  • , Hal Blumenfeld

Research output: Contribution to journalArticlepeer-review

Abstract

The thalamus plays diverse roles in cortical-subcortical brain activity patterns. Recent work suggests that focal temporal lobe seizures depress subcortical arousal systems and convert cortical activity into a pattern resembling slow-wave sleep. The potential simultaneous and paradoxical role of the thalamus in both limbic seizure propagation, and in sleep-like cortical rhythms has not been investigated.We recorded neuronal activity from the central lateral (CL), anterior (ANT), and ventral posteromedial (VPM) nuclei of the thalamus in an established female rat model of focal limbic seizures. We found that population firing of neurons in CL decreased during seizures while the cortex exhibited slow waves. In contrast, ANT showed a trend toward increased neuronal firing compatible with polyspike seizure discharges seen in the hippocampus. Meanwhile,VPMexhibited a remarkable increase in sleep spindles during focal seizures. Single-unit juxtacellular recordings from CL demonstrated reduced overall firing rates, but a switch in firing pattern from single spikes to burst firing during seizures. These findings suggest that different thalamic nuclei play very different roles in focal limbic seizures. While limbic nuclei, such as ANT, appear to participate directly in seizure propagation, arousal nuclei, such as CL, may contribute to depressed cortical function, whereas sleep spindles in relay nuclei, such as VPM, may interrupt thalamocortical information flow. These combined effects could be critical for controlling both seizure severity and impairment of consciousness. Further understanding of differential effects of seizures on different thalamocortical networks may lead to improved treatments directly targeting these modes of impaired function.

Original languageEnglish
Pages (from-to)11441-11454
Number of pages14
JournalJournal of Neuroscience
Volume37
Issue number47
DOIs
Publication statusPublished - 22 Nov 2017
Externally publishedYes

Keywords

  • Burst firing
  • Consciousness
  • Juxtacellular recording
  • Sleep
  • Temporal lobe epilepsy
  • Thalamus

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