Transcriptomics in the nucleus accumbens shell reveal sex- and reinforcer-specific signatures associated with morphine and sucrose craving

• Published in: Neuropsychopharmacology (New York, N.Y.) N.Y.), 2022-09, Vol.47 (10), p.1764-1775
• Main Authors: Mayberry, Hannah L, Bavley, Charlotte C, Karbalaei, Reza, Peterson, Drew R, Bongiovanni, Angela R, Ellis, Alexandra S, Downey, Sara H, Toussaint, Andre B, Wimmer, Mathieu E
• Format: Article
• Language: English
• Subjects: Adaptation; Analgesics, Opioid - metabolism; Analgesics, Opioid - pharmacology; Animals; Conditioning, Operant; Craving; Cues; Drug addiction; Drug self-administration; Drug-Seeking Behavior; Female; Gender differences; Gene expression; Male; Morphine; Morphine - metabolism; Narcotics; Nucleus Accumbens; Opioids; Rats; Reinforcement; Self Administration; Sex differences; Sucrose; Sucrose - pharmacology; Therapeutic targets; Transcriptome; Transcriptomics
• ISSN: 0893-133X; 1740-634X
• DOI: 10.1038/s41386-022-01289-2

Incubation of craving is a well-documented phenomenon referring to the intensification of drug craving over extended abstinence. The neural adaptations that occur during forced abstinence following chronic drug taking have been a topic of intense study. However, little is known about the transcriptomic changes occurring throughout this window of time. To define gene expression changes associated with morphine consumption and extended abstinence, male and female rats underwent 10 days of morphine self-administration. Separate drug-naive rats self-administered sucrose in order to compare opioid-induced changes from those associated with natural, non-drug rewards. After one or 30 days of forced abstinence, rats were tested for craving, or nucleus accumbens shell tissue was dissected for RNA sequencing. Morphine consumption was predictive of drug seeking after extended (30 days) but not brief (1 day) abstinence in both sexes. Extended abstinence was also associated with robust sex- and reinforcer-specific changes in gene expression, suggesting sex differences underlying incubation of morphine and sucrose seeking respectively. Importantly, these changes in gene expression occurred without re-exposure to drug-paired cues, indicating that chronic morphine causes long-lasting changes in gene expression that prime the system for increased craving. These findings lay the groundwork for identifying specific therapeutic targets for curbing opioid craving without impacting the natural reward system in males and females.