Electrical stimulation of the endopiriform nucleus attenuates epilepsy in rats by network modulation

Ann Clin Transl Neurol. 2020 Dec;7(12):2356-2369. doi: 10.1002/acn3.51214. Epub 2020 Oct 31.

Abstract

Objective: Neuromodulatory anterior thalamic deep brain stimulation (DBS) is an effective therapy for intractable epilepsy, but few patients achieve complete seizure control with thalamic DBS. Other stimulation sites may be considered for anti-seizure DBS. We investigated bilateral low-frequency stimulation of the endopiriform nuclei (LFS-EPN) to control seizures induced by intracortically implanted cobalt wire in rats.

Methods: Chronic epilepsy was induced by cobalt wire implantation in the motor cortex unilaterally. Bipolar-stimulating electrodes were implanted into the EPN bilaterally. Continuous electroencephalography (EEG) was recorded using electrodes placed into bilateral motor cortex and hippocampus CA1 areas. Spontaneous seizures were monitored by long-term video-EEG, and behavioral seizures were classified based on the Racine scale. Continuous 1-Hz LFS-EPN began on the third day after electrode implantation and was controlled by a multi-channel stimulator. Stimulation continued until the rats had no seizures for three consecutive days.

Results: Compared with the control and sham stimulation groups, the LFS-EPN group experienced significantly fewer seizures per day and the mean Racine score of seizures was lower due to fewer generalized seizures. Ictal discharges at the epileptogenic site had significantly reduced theta band power in the LFS-EPN group compared to the other groups.

Interpretation: Bilateral LFS-EPN attenuates cobalt wire-induced seizures in rats by modulating epileptic networks. Reduced ictal theta power of the EEG broadband spectrum at the lesion site may be associated with the anti-epileptogenic mechanism of LFS-EPN. Bilateral EPN DBS may have therapeutic applications in human partial epilepsies.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CA1 Region, Hippocampal / physiopathology
  • Deep Brain Stimulation
  • Disease Models, Animal
  • Electric Stimulation Therapy*
  • Electrocorticography
  • Epilepsy / therapy*
  • Implantable Neurostimulators
  • Male
  • Motor Cortex / physiopathology*
  • Piriform Cortex*
  • Rats
  • Rats, Sprague-Dawley
  • Seizures
  • Theta Rhythm / physiology*

Grants and funding

This work was funded by National Natural Science Foundation of China grants XFY 81471391, XFY 81671367, XFY 81790653, and XFY 81971202.