AI Article Synopsis

  • The rise of synthetic cannabinoids (SCBs) poses a serious public health risk, as they produce similar psychoactive effects to THC but with unpredictable side effects and a potential for addiction.
  • Despite being marketed as legal and safe, SCBs are poorly regulated due to a lack of scientific research on their harmful effects.
  • A study using an intravenous self-administration (IVSA) method in rats showed that two SCBs (AM-1248 and CB-13) exhibited strong reinforcing effects, indicating significant abuse potential and impulsive behavior.

Article Abstract

Currently, the expanding recreational use of synthetic cannabinoids (SCBs) threatens public health. SCBs produce psychoactive effects similar to those of tetrahydrocannabinol, the main component of cannabis, and additionally induce unexpected pharmacological side effects. SCBs are falsely advertised as legal and safe, but in reality, SCB abuse has been reported to cause acute intoxication and addictive disorders. However, because of the lack of scientific evidence to elucidate their dangerous pharmacological effects, SCBs are weakly regulated and continue to circulate in illegal drug markets. In the present study, the intravenous self-administration (IVSA) paradigm was used to evaluate the abuse potential of three SCBs (AM-1248, CB-13, and PB-22) in rats. All three SCBs maintained IVSA with a large number of infusions and active lever presses, demonstrating their reinforcing effects. The increase of active lever presses was particularly significant during the early IVSA sessions, indicating the reinforcementenhancing effects of the SCBs (AM-1248 and CB-13). The number of inactive lever presses was significantly higher in the SCB groups (AM-1248 and CB-13) than that in the vehicle group, indicating their impulsive effects. In summary, these results demonstrated that SCBs have distinct pharmacological properties and abuse potential.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8255142PMC
http://dx.doi.org/10.4062/biomolther.2020.212DOI Listing

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