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• W3097586099 abstract "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." @default.
• W3097586099 created "2020-11-09" @default.
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• W3097586099 date "2020-10-31" @default.
• W3097586099 modified "2023-10-16" @default.
• W3097586099 title "Electrical stimulation of the endopiriform nucleus attenuates epilepsy in rats by network modulation" @default.
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• W3097586099 doi "https://doi.org/10.1002/acn3.51214" @default.
• W3097586099 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/7732253" @default.
• W3097586099 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/33128504" @default.
• W3097586099 hasPublicationYear "2020" @default.
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