Endocannabinoid genetic variation enhances vulnerability to THC reward in adolescent female mice.
Caitlin E BurgdorfDeqiang JingRuirong YangChienchun HuangMatthew N HillKen MackieTeresa A MilnerVirginia M PickelFrancis S LeeAnjali M RajadhyakshaPublished in: Science advances (2020)
Adolescence represents a developmental period with the highest risk for initiating cannabis use. Little is known about whether genetic variation in the endocannabinoid system alters mesolimbic reward circuitry to produce vulnerability to the rewarding properties of the exogenous cannabinoid Δ9-tetrahydrocannabinol (THC). Using a genetic knock-in mouse model (FAAHC/A) that biologically recapitulates the human polymorphism associated with problematic drug use, we find that in adolescent female mice, but not male mice, this FAAH polymorphism enhances the mesolimbic dopamine circuitry projecting from the ventral tegmental area (VTA) to the nucleus accumbens (NAc) and alters cannabinoid receptor 1 (CB1R) levels at inhibitory and excitatory terminals in the VTA. These developmental changes collectively increase vulnerability of adolescent female FAAHC/A mice to THC preference that persists into adulthood. Together, these findings suggest that this endocannabinoid genetic variant is a contributing factor for increased susceptibility to cannabis dependence in adolescent females.
Keyphrases
- young adults
- mental health
- climate change
- high fat diet induced
- mouse model
- depressive symptoms
- genome wide
- prefrontal cortex
- endothelial cells
- childhood cancer
- transcription factor
- type diabetes
- insulin resistance
- adipose tissue
- spinal cord injury
- wild type
- gene expression
- dna methylation
- early life
- deep brain stimulation
- pluripotent stem cells