Abstract
Objective
Tuberous sclerosis complex (TSC) is one of the most common genetic causes of epilepsy. Seizures in TSC typically first present in infancy or early childhood, including focal seizures and infantile spasms. Infantile spasms in TSC are particularly characteristic in its strong responsiveness to vigabatrin. Although a number of mouse models of epilepsy in TSC have been described, there are very limited electroencephalographic (EEG) or seizure data during the preweanling neonatal and infantile‐equivalent mouse periods. Tsc1
GFAPCKO mice are a well‐characterized mouse model of epilepsy in TSC, but whether these mice have seizures during early development has not been documented. The objective of this study was to determine whether preweanling Tsc1
GFAPCKO mice have developmental EEG abnormalities or seizures, including spasms.
Methods
Longitudinal video‐EEG and electromyographic recordings were performed serially on Tsc1
GFAPCKO and control mice from postnatal days 9‐21 and analyzed for EEG background abnormalities, sleep‐wake vigilance states, and spontaneous seizures. Spasms were also induced with varying doses of N‐methyl‐D‐aspartate (NMDA).
Results
The interictal EEG of Tsc1
GFAPCKO mice had excessive discontinuity and slowing, suggesting a delayed developmental progression compared with control mice. Tsc1
GFAPCKO mice also had increased vigilance state transitions and fragmentation. Tsc1
GFAPCKO mice had spontaneous focal seizures in the early neonatal period and a reduced threshold for NMDA‐induced spasms, but no spontaneous spasms were observed.
Significance
Neonatal Tsc1
GFAPCKO mice recapitulate early developmental aspects of EEG abnormalities, focal seizures, and an increased propensity for spasms. This mouse model may be useful for early mechanistic and therapeutic studies of epileptogenesis in TSC.
ABR