Intermittent intake of rapid cocaine injections promotes the risk of relapse and increases mesocorticolimbic BDNF levels during abstinence

• Published in: Neuropsychopharmacology (New York, N.Y.) N.Y.), 2019-05, Vol.44 (6), p.1027-1035
• Main Authors: Gueye, Aliou B, Allain, Florence, Samaha, Anne-Noël
• Format: Article
• Language: English
• Subjects: Addictions; Animals; Behavior, Animal - drug effects; Behavior, Animal - physiology; Brain; Brain - drug effects; Brain - metabolism; Brain - physiopathology; Brain-derived neurotrophic factor; Brain-Derived Neurotrophic Factor - metabolism; Cocaine; Cocaine - administration & dosage; Cocaine - pharmacology; Cocaine-Related Disorders - metabolism; Cocaine-Related Disorders - physiopathology; Conditioning; Craving - drug effects; Craving - physiology; Cues; Disease Models, Animal; Dopamine Uptake Inhibitors - administration & dosage; Dopamine Uptake Inhibitors - pharmacology; Drug abuse; Drug addiction; Intravenous administration; Narcotics; Nucleus accumbens; Nucleus Accumbens - drug effects; Nucleus Accumbens - metabolism; Nucleus Accumbens - physiopathology; Prefrontal Cortex - drug effects; Prefrontal Cortex - metabolism; Prefrontal Cortex - physiopathology; Rats; Reinforcement; Reinstatement; Reward; Rodents; Schedules; Self Administration; Time Factors; Ventral Tegmental Area - drug effects; Ventral Tegmental Area - metabolism; Ventral Tegmental Area - physiopathology; Ventral tegmentum; Withdrawal
• ISSN: 0893-133X; 1740-634X
• DOI: 10.1038/s41386-018-0249-8

Cocaine is thought to be more addictive when it reaches the brain rapidly. We predicted that variation in the speed of cocaine delivery influences the likelihood of addiction in part by determining the risk of relapse after abstinence. Under an intermittent-access schedule, rats pressed a lever for rapid (injected over 5 s) or slower (90 s) intravenous cocaine injections (0.5 mg/kg/injection). Control rats self-administered food pellets. A tone-light cue accompanied each self-administered reward. The 5s- and 90s-rats took a similar average amount of cocaine. One or 45 days after withdrawal from cocaine/forced abstinence, lever-pressing behaviour was extinguished during a 6-h session. Immediately thereafter, cue- or cocaine (10 mg/kg, i.p.)-induced reinstatement was assessed for 1 h. One or 45 days after withdrawal, only 5s-rats showed significant cocaine-induced reinstatement of reward-seeking behaviour. In both cocaine groups, cue-induced reinstatement behaviour was more pronounced after 45 days than after 1 day of withdrawal from cocaine, indicating incubation of conditioned drug craving. However, cue-induced reinstatement after extended abstinence was greatest in the 5s-rats. Brain-derived neurotrophic factor (BDNF) activity in the brain regulates reinstatement behaviour. Thus, 24 h after reinstatement tests, we measured BDNF protein concentrations in mesocorticolimbic regions. Only 5s-rats showed time-dependent increases in BDNF concentrations in the prelimbic cortex, nucleus accumbens core and ventral tegmental area after withdrawal from cocaine (day 45 > day 1). Thus, rapidly rising brain cocaine levels might facilitate addiction by evoking changes in the brain that intensify drug craving after abstinence, and these changes persist long after the last bout of cocaine use.