文摘
Sucrose reinforcement in rats was used as a preclinical model for food consumption upon nicotine-dosing discontinuation. Nicotine (0.4 mg/kg) enhanced sucrose reinforcement and devalued sucrose reinforcement upon discontinuation of dosing. Naloxone (0.3 & 3.0 mg/kg) attenuated reinforcement enhancement by nicotine, but did not prevent devaluation by nicotine. The highest dose of naloxone (3.0 mg/kg) in combination with nicotine, interfered with sucrose reinforcement during dosing. Opioid antagonism by itself did not interfere with sucrose reinforcement at the doses used. Discontinuation of the higher (3.0 mg/kg) but not lower (0.3 mg/kg) dose of naloxone, devalued sucrose reinforcement.