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| Cannabidiol reduces seizures following CNS infection with Theiler's murine encephalomyelitis virus.
Patel DC1, Wallis G1, Fujinami RS2, Wilcox KS1,3, Smith MD1,3,4.
Author information
1Department of Pharmacology & Toxicology University of Utah Salt Lake City Utah.2Department of Pathology University of Utah Salt Lake City Utah.3Anticonvulsant Drug Development Program University of Utah Salt Lake City Utah.4School of Dentistry University of Utah Salt Lake City Utah.
Abstract
Objective:
C57BL/6J mice infected with Theiler's murine encephalomyelitis virus (TMEV) develop acute behavioral seizures in the first week of infection and later develop chronic epilepsy. The TMEV model provides a useful platform to test novel antiseizure therapeutics. The present study was designed to test the efficacy of cannabidiol (CBD) in reducing acute seizures induced by viral infection.
Methods:
C57BL/6J mice were infected intracortically with 2 × 105 plaque-forming units of TMEV. Mice were divided into two treatment groups-1) CBD-treated mice and 2) vehicle-treated mice. Frequency and severity of acute seizures were evaluated by video-monitoring the mice four times daily by the experimenter blinded to the treatment group.
Results:
Cannabidiol (180 mg/kg; 360 mg/kg/day) decreased both the frequency and severity of acute behavioral seizures following TMEV infection, but 150 mg/kg of CBD did not improve overall seizure outcome. The time to peak effect (TPE) of CBD in the 6 Hz 32 mA psychomotor seizure test using C57BL/6J mice was observed at 2 hours post-CBD treatment. Interestingly, CBD (150 mg/kg) significantly reduced frequency and severity of TMEV-induced acute seizures at 2 hours post-CBD treatment. These results suggest that CBD could be effective in decreasing TMEV-induced acute seizures when the seizure test is conducted at the TPE of CBD.
Significance:
Cannabinoids are increasingly studied for their potential antiseizure effects. Several preclinical and clinical studies provide evidence that CBD could be an effective therapy for intractable epilepsies. The present study corroborates those previous findings and provides an opportunity to investigate pharmacokinetics, pharmacodynamics, and mechanism(s) of antiseizure effects of CBD in the TMEV model, which may help to design future clinical studies more effectively.www.ncbi.nlm.nih.gov/pubmed/31440724  www.ncbi.nlm.nih.gov/pmc/articles/PMC6698680/
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