Key Findings:  The results of this study demonstrate that the anti-inflammatory effect of β-caryophyllene (BCP) involves CB2 and the PPARγ pathway and suggest BCP as a possible therapy for the treatment of inflammatory bowel disease. AM630 and the PPARγ antagonist GW9662 significantly reversed the protective effect of BCP.
Type of Study:  Animal Study
Study Result:  Positive
Study Location(s):  Brazil
Year of Pub:  2011
Cannabinoids Studied:  AM-x Synthetic Cannabinoids, Synthetic Cannabinoid (unspecified)
Phytocannabinoid Source:  Not Applicable
Terpenes Studied:  ß-Caryophyllene
Receptors Studied:  CB2, PPAR - Gamma
Ligands Studied:  Anti-inflammatory cytokines, Pro-inflammatory cytokines
Dosage: Animals were orally treated by gavage with 12.5, 25, or 50 mg/kg of BCP twice a day from day 0 to day 7 (preventive treatment) or with 50 mg/kg from day 3 to day 7 (therapeutic treatment).
Route of Administration:  Oral (Ingestion)