Graduate Program in Neuroscience, Yerkes National Primate Research Center, Departments of Pediatrics and Psychiatry and Behavioral Sciences, Emory University, 954 Gatewood Dr. NE, Atlanta, GA, 30329, USA.
Graduate Program in Molecular and Systems Pharmacology, Emory University, Atlanta, GA, USA.
Neurotherapeutics. 2020 Jan;17(1):165-177. doi: 10.1007/s13311-019-00752-1.
Cocaine use during adolescence decreases the likelihood that individuals will seek treatment for recurrent drug use. In rodents, developmental cocaine exposure weakens action-consequence decision-making, causing a deferral to familiar, habit-like behavioral response strategies. Here, we aimed to improve action-outcome decision-making. We found that acute pharmacological stimulation of the tyrosine/tropomyosin receptor kinase B (trkB) via 7,8-dihydroxyflavone (7,8-DHF) or 3,4-methylenedioxymethamphetamine (MDMA) blocked cocaine-induced habit biases by strengthening memory for action-outcome associations. We believe that MDMA acts by stimulating neurotrophin/trkB systems in the orbitofrontal cortex (OFC), a region involved in prospectively evaluating the consequences of one's action, because 1) MDMA also increased brain-derived neurotrophic factor (BDNF) in the OFC, 2) MDMA corrected habit biases due to Bdnf loss in the OFC, and 3) overexpression of a truncated isoform of trkB occluded the memory-enhancing effects of MDMA. Thus, selecting actions based on their consequences requires BDNF-trkB in the OFC, the stimulation of which may improve goal attainment in both drug-naïve and cocaine-exposed individuals. SIGNIFICANCE STATEMENT: Cocaine use during adolescence decreases the likelihood that individuals will seek treatment for recurrent drug use, even as adults. Understanding how early-life cocaine exposure impacts goal-oriented action and prospective decision-making in adulthood is thus important. One key aspect of goal-directed decision-making is anticipating the consequences of one's actions, a process that likely involves the orbitofrontal cortex (OFC). In rodents, developmental cocaine exposure weakens action-consequence decision-making, causing a deferral to familiar, habit-like behavioral response strategies. Here, we report that we can improve memory for action-consequence relationships by stimulating neurotrophic factors, which support cell survival, development, and plasticity in the brain. With strengthened action-consequence associations, cocaine-exposed mice regain the ability to optimally select actions based on their likely outcomes. Brain region-selective manipulations reveal that neurotrophin systems in the OFC are necessary for stable memory of action-consequence relationships.
青少年时期使用可卡因会降低个体寻求复发性药物使用治疗的可能性。在啮齿动物中,发育性可卡因暴露会削弱行为-后果决策,导致对熟悉的、习惯化的行为反应策略的延迟。在这里,我们旨在改善行为-结果决策。我们发现,通过 7,8-二羟基黄酮(7,8-DHF)或 3,4-亚甲二氧基甲基苯丙胺(MDMA)急性药理学刺激酪氨酸/原肌球蛋白受体激酶 B(trkB),通过加强对行为-结果关联的记忆,阻断可卡因引起的习惯偏差。我们认为,MDMA 通过刺激眶额皮质(OFC)中的神经营养因子/trkB 系统发挥作用,OFC 是一个参与前瞻性评估一个人行为后果的区域,因为 1)MDMA 还增加了 OFC 中的脑源性神经营养因子(BDNF),2)MDMA 纠正了由于 OFC 中 Bdnf 缺失而导致的习惯偏差,3)trkB 截断异构体的过表达阻断了 MDMA 的增强记忆作用。因此,基于后果选择行为需要 OFC 中的 BDNF-trkB,其刺激可能会提高药物-naïve 和可卡因暴露个体的目标实现。
青少年时期使用可卡因会降低个体寻求复发性药物使用治疗的可能性,即使成年后也是如此。因此,了解早期可卡因暴露如何影响成年期以目标为导向的行为和前瞻性决策非常重要。目标导向决策的一个关键方面是预测一个人的行为后果,这个过程可能涉及眶额皮质(OFC)。在啮齿动物中,发育性可卡因暴露会削弱行为-后果决策,导致对熟悉的、习惯化的行为反应策略的延迟。在这里,我们报告说,我们可以通过刺激神经营养因子来改善对行为-后果关系的记忆,神经营养因子支持大脑中的细胞存活、发育和可塑性。通过加强行为-后果关联,可卡因暴露的小鼠重新获得了根据可能的结果优化选择行为的能力。大脑区域选择性操作表明,OFC 中的神经营养因子系统对于行为-后果关系的稳定记忆是必要的。