Cannabidiol is a behavioral modulator in BTBR mouse model of idiopathic autism

Sarah H Shrader1, Nicholas Mellen2, Jun Cai1,3

  • 1Department of Pharmacology and Toxicology, University of Louisville School of Medicine, Louisville, KY, United States.

PubMed

Insights

Cannabidiol (CBD) effectively reduced autism-like behaviors in mice. Different CBD doses targeted specific symptoms, suggesting its potential for treating repetitive behaviors, social deficits, and hyperactivity in Autism Spectrum Disorder (ASD).

Area of Science:

  • Neuroscience
  • Pharmacology
  • Genetics

Background:

  • Autism Spectrum Disorder (ASD) prevalence is increasing, affecting 1 in 36 U.S. children.
  • Core ASD symptoms include social interaction deficits, communication problems, and repetitive behaviors.
  • Current pharmacological treatments for core ASD symptoms are lacking.

Purpose of the Study:

  • To investigate the effects of Cannabidiol (CBD) on autism-like behaviors in BTBR mice, an established model for idiopathic ASD.
  • To determine if CBD can attenuate core ASD-like behaviors and associated comorbidities.

Main Methods:

  • Male BTBR mice received daily intraperitoneal injections of vehicle, 20 mg/kg CBD, or 50 mg/kg CBD for two weeks.
  • Behavioral assays were conducted on the final treatment day to assess CBD's effects.
  • CBD's impact was compared to age-matched, vehicle-treated C57BL/6J mice.

Main Results:

  • High-dose (50 mg/kg) CBD significantly reduced repetitive self-grooming and hyperactivity in BTBR mice.
  • Low-dose (20 mg/kg) CBD treatment ameliorated social deficits in BTBR mice.
  • CBD demonstrated dose-dependent effects on specific autism-related behaviors.

Conclusions:

  • Different CBD dosages may be required to effectively treat distinct ASD-related behaviors.
  • CBD shows promise as a potential therapeutic agent for ameliorating repetitive behaviors, social deficits, and hyperactivity associated with ASD.
  • Further research is warranted to explore CBD's efficacy in managing core ASD symptoms and comorbidities.
Abstract