Interdisciplinary Graduate Program in Neuroscience, University of Iowa, Iowa City, IA, 52242, USA.
Department of Psychological and Brain Sciences, University of Iowa, Iowa City, IA, 52242, USA.
Neuropsychopharmacology. 2024 Sep;49(10):1540-1549. doi: 10.1038/s41386-024-01846-x. Epub 2024 Mar 18.
Evidence indicates that the anterior (aIC), but not posterior (pIC), insular cortex promotes cued reinstatement of cocaine seeking after extinction in rats. It is unknown whether these subregions also regulate heroin seeking and whether such involvement depends on prior extinction learning. To address these questions, we used baclofen and muscimol (BM) to inactivate the aIC or pIC bilaterally during a seeking test after extinction or prolonged withdrawal from heroin. Male Sprague-Dawley rats in the extinction groups underwent 10+ days of heroin self-administration, followed by 6+ days of extinction sessions, and subsequent cued or heroin-primed reinstatement. Results indicate that aIC inactivation increased cued reinstatement of heroin seeking after extinction, whereas pIC inactivation prevented cued reinstatement. To determine whether these effects were extinction-dependent, we conducted a subsequent study using both sexes with prolonged withdrawal. Male and female rats in the withdrawal groups underwent 10+ days of heroin self-administration, followed by cued seeking tests after 1 and 14 days of homecage withdrawal to measure incubation of heroin craving. In this case, the findings indicate that aIC inactivation had no effect on incubation of heroin craving after withdrawal in either sex, whereas pIC inactivation decreased heroin craving only in males. These findings suggest that the aIC and pIC have opposing roles in suppressing vs promoting cued heroin seeking after extinction and that these roles are distinct from those in cocaine seeking. Moreover, the incubation of craving results suggest that new contingency learning is necessary to recruit the aIC in cued heroin seeking.
证据表明,在前脑岛(aIC),而不是后脑岛(pIC),促进了可卡因寻求的线索复燃,而在大鼠中,可卡因寻求的线索复燃是在消退之后发生的。目前尚不清楚这些亚区是否也调节海洛因的寻求,以及这种参与是否取决于之前的消退学习。为了解决这些问题,我们在消退或海洛因长期戒断后进行的寻求测试中,使用巴氯芬和毒蕈碱(BM)双侧失活 aIC 或 pIC。在消退组中,雄性 Sprague-Dawley 大鼠接受了 10 多天的海洛因自我给药,然后进行了 6 多天的消退疗程,随后进行了线索或海洛因引发的复燃。结果表明,aIC 失活增加了消退后海洛因寻求的线索复燃,而 pIC 失活则阻止了线索复燃。为了确定这些影响是否依赖于消退,我们使用延长戒断的雌雄大鼠进行了后续研究。在戒断组中,雄性和雌性大鼠接受了 10 多天的海洛因自我给药,然后在 1 天和 14 天的笼内戒断后进行线索寻求测试,以测量海洛因渴望的潜伏期。在这种情况下,研究结果表明,aIC 失活对两性海洛因渴望的潜伏期没有影响,而 pIC 失活仅在雄性中降低了海洛因渴望。这些发现表明,aIC 和 pIC 在抑制和促进消退后线索海洛因寻求方面具有相反的作用,而且这些作用与可卡因寻求不同。此外,渴望的潜伏期结果表明,在线索海洛因寻求中,需要新的条件反射学习来招募 aIC。