Sex- and genotype-dependent nicotine plus cue-primed reinstatement is enhanced in adolescent Sprague Dawley rats containing the human 6 3'-UTR polymorphism (rs2304297).

RATIONALE

Large-scale human candidate gene studies have indicated that a genetic variant (rs2304297) in the alpha(α)6 nicotinic acetylcholine receptor (nAChR) subunit, encoded by the 6 gene, may play a key role in adolescent nicotine addictive behavior. We hypothesized that the polymorphism selectively enhances nicotine + cue-primed reinstatement, but not nicotine- or cue-reinstatement in α6 (risk) vs. α6 (non-risk) allele carriers, without having baseline effects on natural rewards.

METHODS

Using CRISPR-Cas9 genomic engineering, we developed a humanized rat line with the human gene variant of the 6 3'-UTR polymorphism in Sprague-Dawley rats. Genetically modified adolescent male and female rats were food trained under a fixed-ratio (FR)1 schedule of reinforcement and progressively increased to FR5. Animals were implanted with catheters and began nicotine self-administration (15 μg/kg/infusion) at FR5. Upon reaching stable responding, reinforced behavior was extinguished by removal of drug and cues. Reinstatement testing began for cue only, nicotine only, and nicotine + cue in a Latin Square Design. Animals were returned to extinction conditions for 2 days minimum between testing.

RESULTS

For natural food rewards, nicotine self-administration, progressive ratio, and extinction, adolescent male and female (α6 and α6 ) rats exhibited equivalent behaviors. Male α6 rats show enhanced nicotine + cue-primed reinstatement when compared with male α6 rats. This genotype effect on reinstatement was not seen in female rats.

CONCLUSION

Our findings support the functional role of the human 6 3'-UTR SNP genetic variant in sex-dependently enhancing nicotine seeking behavior in adolescent rats. Overall, the findings support clinical and preclinical data highlighting a role of α6 nAChRs mediating sex heterogeneity in substance use and related phenotypes.