Source Paper
Cannabidiol attenuates seizures and social deficits in a mouse model of Dravet syndrome
Joshua S. Kaplan, Nephi Stella, William A. Catterall, Ruth E. Westenbroek
Proceedings of the National Academy of Sciences • 2017
View Abstract
Significance Medicinal cannabis use is booming despite limited preclinical evidence and mechanistic insight. Recent clinical trials of cannabidiol (CBD) in Dravet syndrome (DS) support its clinical efficacy for reduction of seizure frequency and invite study of its benefits for additional DS symptoms. We demonstrate here that treatment with CBD is beneficial for seizure frequency, duration, and severity and for autistic-like social deficits in a mouse model of DS. CBD rescue of DS symptoms is associated with increased inhibitory neurotransmission, potentially mediated by antagonism of the lipid-activated G protein-coupled receptor GPR55. These studies lend critical support for treatment of seizures in DS with CBD, extend the scope of CBD treatment to autistic-like behaviors, and provide initial mechanistic insights into CBD’s therapeutic actions.
Spontaneous Seizure Monitoring
Objective: Quantification of the frequency of spontaneous seizures occurring in Dravet syndrome mice to assess the effects of cannabidiol (CBD) treatment on seizure phenotype
Protocol Steps
Spontaneous Seizure Monitoring
Monitor and quantify the frequency of spontaneous seizures occurring in Dravet syndrome mice during the experimental period
Note: The frequency of spontaneous seizures was measured as a primary outcome to assess CBD treatment effects
View evidence from paper
“the frequency of spontaneous seizures were substantially decreased”