Department of Neuroscience, Psychiatry, and Psychology, Center for Neuroscience, University of Pittsburgh, Pittsburgh, PA, USA.
Neuropsychopharmacology. 2022 Nov;47(12):2090-2100. doi: 10.1038/s41386-022-01387-1. Epub 2022 Jul 23.
Strategy switching is a form of cognitive flexibility that requires inhibiting a previously successful strategy and switching to a new strategy of a different categorical modality. It is dependent on dopamine (DA) receptor activation and release in ventral striatum and prefrontal cortex, two primary targets of ventral tegmental area (VTA) DA projections. Although the circuitry that underlies strategy switching early in learning has been studied, few studies have examined it after extended discrimination training. This may be important as DA activity and release patterns change across learning, with several studies demonstrating a critical role for substantia nigra pars compacta (SNc) DA activity and release once behaviors are well-learned. We have demonstrated that medial septum (MS) activation simultaneously increased VTA and decreased SNc DA population activity, as well as improved reversal learning via these actions on DA activity. We hypothesized that MS activation would improve strategy switching both early in learning and after extended training through its ability to increase VTA DA population activity and decrease SNc DA population activity, respectively. We chemogenetically activated the MS of male and female rats and measured their performance on an operant-based strategy switching task following 1, 10, or 15 days of discrimination training. Contrary to our hypothesis, MS activation did not affect strategy switching after 1 day of discrimination training. MS activation improved strategy switching after 10 days of training, but only in females. MS activation improved strategy switching in both sexes after 15 days of training. Infusion of bicuculline into the ventral subiculum (vSub) inhibited the MS-mediated decrease in SNc DA population activity and attenuated the improvement in strategy switching. Intra-vSub infusion of scopolamine inhibited the MS-mediated increase in VTA DA population activity but did not affect the improvement in strategy switching. Intra-vSub infusion of both bicuculline and scopolamine inhibited the MS-mediated effects on DA population activity in both the SNc and VTA and completely prevented the improvement in strategy switching. These data indicate that MS activation improves strategy switching once the original strategy has been sufficiently well-learned, and that this may occur via the MS's regulation of DA neuron responsivity.
策略转换是一种认知灵活性形式,需要抑制先前成功的策略并切换到不同范畴模式的新策略。它依赖于腹侧被盖区 (VTA) DA 投射的腹侧纹状体和前额叶皮层中的多巴胺 (DA) 受体激活和释放,这两个区域是 VTA DA 投射的两个主要靶点。尽管在学习早期已经研究了支持策略转换的回路,但很少有研究在经过扩展的辨别训练后对其进行研究。这可能很重要,因为随着学习的进行,DA 活动和释放模式会发生变化,有几项研究表明,一旦行为得到很好的学习,黑质致密部 (SNc) DA 活动和释放就起着关键作用。我们已经证明,内侧隔核 (MS) 的激活同时增加了 VTA 和减少了 SNc DA 群体活动,并且通过对 DA 活动的这些作用改善了反转学习。我们假设,MS 的激活通过增加 VTA DA 群体活动和减少 SNc DA 群体活动的能力,将分别在学习早期和经过扩展的训练后改善策略转换。我们通过化学遗传方法激活雄性和雌性大鼠的 MS,并在经过 1、10 或 15 天的辨别训练后测量它们在操作性策略转换任务上的表现。与我们的假设相反,MS 的激活并没有影响在 1 天的辨别训练后的策略转换。MS 的激活在经过 10 天的训练后改善了策略转换,但仅在雌性中。MS 的激活在经过 15 天的训练后改善了两性的策略转换。将毒蕈碱受体拮抗剂印防己毒素注入腹侧下托 (vSub) 抑制了 MS 介导的 SNc DA 群体活动的减少,并减弱了策略转换的改善。在 vSub 内注射东莨菪碱抑制了 MS 介导的 VTA DA 群体活动的增加,但不影响策略转换的改善。在 vSub 内同时注射印防己毒素和东莨菪碱抑制了 MS 对 SNc 和 VTA 中 DA 群体活动的影响,并完全阻止了策略转换的改善。这些数据表明,一旦最初的策略得到充分的学习,MS 的激活就会改善策略转换,而这可能是通过 MS 对 DA 神经元反应性的调节来实现的。