Altered neuronal activity in the ventromedial prefrontal cortex drives nicotine intake escalation

Nicotine addiction develops after prolonged drug use and escalation of drug intake. However, because of difficulties in demonstrating escalation of nicotine use in rats, its underlying neuroadaptations still remain poorly understood. Here we report that access to unusually high doses of nicotine (i.e., from 30 mu g to 240 mu g/kg/injection) for self-administration precipitated a rapid and robust escalation of nicotine intake and increased the motivation for the drug in rats. This nicotine intake escalation also induced long-lasting changes in vmPFC neuronal activity both before and during nicotine self-administration. Specifically, after escalation of nicotine intake, basal vmPFC neuronal activity increased above pre-escalation and control activity levels, while ongoing nicotine self-administration restored these neuronal changes. Finally, simulation of the restoring effects of nicotine with in vivo optogenetic inhibition of vmPFC neurons caused a selective de-escalation of nicotine self-administration.

Automated summary

Nicotine addiction develops after prolonged drug use and escalation of drug intake. Access to unusually high doses of nicotine leads to a rapid escalation of nicotine intake and increased motivation for the drug in rats. This escalation also induces long-lasting changes in specific neuronal activity in the brain.