Department of Pharmacology & Toxicology, Neuroscience Research Center, Medical College of Wisconsin, Milwaukee, WI, USA.
Departments of Pharmacology & Toxicology and Neurosurgery, Neuroscience Research Center, Medical College of Wisconsin, Milwaukee, WI, USA.
Transl Psychiatry. 2024 Sep 23;14(1):387. doi: 10.1038/s41398-024-03068-7.
The dorsal medial prefrontal cortex (dmPFC) plays a dual role in modulating drug seeking and fear-related behaviors. Learned associations between cues and drug seeking are encoded by a specific ensemble of neurons. This study explored the stability of a dmPFC cocaine seeking ensemble over 2 weeks and its influence on persistent cocaine seeking and fear memory retrieval. In the first series of experiments, we trained TetTag c-fos-driven-EGFP mice in cocaine self-administration and tagged strongly activated neurons with EGFP during the initial day 7 cocaine seeking session. Subsequently, a follow-up seeking test was conducted 2 weeks later to examine ensemble reactivation between two seeking sessions via c-Fos immunostaining. In the second series of experiments, we co-injected viruses expressing TRE-cre and a cre-dependent inhibitory PSAM-GlyR into the dmPFC of male and female c-fos-tTA mice to enable "tagging" of cocaine seeking ensemble or cued fear ensemble neurons with inhibitory chemogenetic receptors. These c-fos-tTA mice have the c-fos promoter that drives expression of the tetracycline transactivator (tTA). The tTA can bind to the tetracycline response element (TRE) site on the viral construct, resulting in the expression of cre-recombinase, which enables the expression of cre-dependent inhibitory chemogenetic receptors and fluorescent reporters. Then we investigated ensemble contribution to subsequent cocaine seeking and fear recall during inhibition of the tagged ensemble by administering uPSEM792s (0.3 mg/kg), a selective ligand for PSAM-GlyR. In both sexes, there was a positive association between the persistence of cocaine seeking and the proportion of reactivated EGFP+ neurons within the dmPFC. More importantly, inhibition of the cocaine seeking ensemble suppressed cocaine seeking, but not recall of fear memory, while inhibition of the fear ensemble reduced conditioned freezing but not cocaine seeking. The results demonstrate that cocaine and fear recall ensembles in the dmPFC are stable, but largely exclusive from one another.
背内侧前额皮质(dmPFC)在调节药物寻求和与恐惧相关的行为方面发挥双重作用。线索和药物寻求之间的习得性关联由特定的神经元集合编码。本研究探讨了 dmPFC 可卡因寻求集合在 2 周内的稳定性及其对持续可卡因寻求和恐惧记忆检索的影响。在一系列实验中,我们在可卡因自我给药中训练 TetTag c-fos 驱动的 EGFP 小鼠,并在初始第 7 天可卡因寻求会议期间使用 EGFP 标记强烈激活的神经元。随后,进行后续的寻求测试,通过 c-Fos 免疫染色检查两个寻求会议之间的集合再激活。在第二系列实验中,我们共注射表达 TRE-cre 和依赖 cre 的抑制性 PSAM-GlyR 的病毒到雄性和雌性 c-fos-tTA 小鼠的 dmPFC 中,以用抑制性化学遗传受体标记可卡因寻求集合或提示恐惧集合神经元。这些 c-fos-tTA 小鼠具有 c-fos 启动子,该启动子驱动四环素转录激活剂(tTA)的表达。tTA 可以与病毒构建体上的四环素反应元件(TRE)位点结合,导致 cre 重组酶的表达,从而使 cre 依赖性抑制性化学遗传受体和荧光报告基因的表达。然后,我们通过给予 uPSEM792s(0.3mg/kg)抑制标记的集合,研究了集合对随后可卡因寻求和恐惧回忆的贡献,uPSEM792s 是 PSAM-GlyR 的选择性配体。在两性中,可卡因寻求的持久性与 dmPFC 内再激活的 EGFP+神经元的比例之间存在正相关。更重要的是,抑制可卡因寻求集合抑制可卡因寻求,但不抑制恐惧记忆的回忆,而抑制恐惧集合则降低条件性冻结,但不抑制可卡因寻求。结果表明,dmPFC 中的可卡因和恐惧回忆集合是稳定的,但彼此之间很大程度上是排他的。