Dual orexin antagonist normalized sleep homeostatic drive, enhanced GABAergic inhibition, and suppressed seizures after traumatic brain injury

• Published in: Sleep (New York, N.Y.) Vol. 45; no. 12; p. 1
• Main Authors: Konduru, Sruthi R, Isaacson, Jesse R, Lasky, Danny J, Zhou, Zihao, Rao, Rohan K, Vattem, Swati S, Rewey, Sophie J, Jones, Mathew V, Maganti, Rama K
• Format: Journal Article
• Language: English
• Published: US Oxford University Press 12-12-2022
• Subjects: Analysis; Animals; Brain; Brain Injuries, Traumatic - complications; Brain Injuries, Traumatic - drug therapy; Convulsions & seizures; Electroencephalography; Epilepsy; GABA; Injuries; Mice; Neurological Disorders; Orexin Receptor Antagonists - pharmacology; Seizures (Medicine); Seizures - drug therapy; Seizures - etiology; Sleep; Sleep - physiology; Sleep disorders; Traumatic brain injury; sleep disorders; NREM delta power; TBI; posttraumatic epilepsy
• ISSN: 0161-8105; 1550-9109
• DOI: 10.1093/sleep/zsac238

Abstract
Study Objectives
Traumatic brain injury (TBI) can result in posttraumatic epilepsy (PTE) and sleep disturbances. We hypothesized that treatment with sleep aids after TBI can ameliorate PTE.
Methods
CD-1 mice underwent controlled cortical impact (CCI), sham injury, or no craniotomy. Sham and CCI groups underwent a monthlong daily treatment with sleep aids including a dual orexin antagonist (DORA-22) or THIP (gaboxadol) or a respective vehicle starting on the day of CCI. We performed continuous EEG (electroencephalography) recordings at week 1 and months 1, 2, and 3 for ~1 week each time. Seizure analysis occurred at all-time points and sleep analysis occurred in week 1 and month-1/2 in all groups. Subsets of CCI and sham groups were subjected to voltageclamp experiments in hippocampal slices to evaluate GABAergic synaptic inhibition.
Results
DORA-22 treatment suppressed seizures in month 1–3 recordings. TBI reduced the amplitude and frequency of miniature inhibitory synaptic currents (mIPSCs) in dentate granule cells and these changes were rescued by DORA-22 treatment. Sleep analysis showed that DORA-22 increased nonrapid eye movement (NREM) sleep during lights-off whereas THIP increased REM sleep during lights-on in week 1. Both treatments displayed subtle changes in time spent in NREM or REM at month-1/2 as well. TBI not only increased normalized EEG delta power (NΔ) at week-1 and month-1 but also resulted in the loss of the homeostatic diurnal oscillation of NΔ, which was restored by DORA-22 but not THIP treatment.
Conclusions
Dual orexin antagonists may have a therapeutic potential in suppressing PTE potentially by enhancing GABAergic inhibition and impacting sleep homeostatic drive.
Graphical Abstract
Graphical Abstract