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首页> 外文期刊>Learning & memory >Modulation of memory consolidation by the basolateral amygdala or nucleus accumbens shell requires concurrent dopamine receptor activation in both brain regions
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Modulation of memory consolidation by the basolateral amygdala or nucleus accumbens shell requires concurrent dopamine receptor activation in both brain regions

机译:基底外侧杏仁核或伏隔核壳对记忆巩固的调节需要在两个大脑区域同时激活多巴胺受体

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摘要

Previous findings indicate that the basolateral amygdala (BLA) and the nucleus accumbens (NAc) interact in influencing memory consolidation. The current study investigated whether this interaction requires concurrent dopamine (DA) receptor activation in both brain regions. Unilateral, right-side cannulae were implanted into the BLA and the ipsilateral NAc shell or core in male Sprague-Dawley rats (similar to 300 g). One week later, the rats were trained on an inhibitory avoidance (IA) task and, 48 h later, they were tested for retention. Drugs were infused into the BLA and NAc shell or core immediately after training. Post-training intra-BLA infusions of DA enhanced retention, as assessed by latencies to enter the shock compartment on the retention test. Infusions of the general DA receptor antagonist cis-Flupenthixol (Flu) into the NAc shell (but not the core) blocked the memory enhancement induced by the BLA infusions of DA. In the reverse experiment, post-training intra-NAc shell infusions of DA enhanced retention and Flu infusions into the BLA blocked the enhancement. These findings indicate that BLA modulation of memory consolidation requires concurrent DA receptor activation in the NAc shell but not the core. Similarly, NAc shell modulation of memory consolidation requires concurrent DA receptor activation in the BLA. Together with previous findings, these results suggest that the dopaminergic innervation of the BLA and NAc shell is critically involved in the modulation of memory consolidation.
机译:先前的发现表明基底外侧杏仁核(BLA)和伏隔核(NAc)在影响记忆巩固中相互作用。目前的研究调查了这种相互作用是否需要在两个大脑区域同时激活多巴胺(DA)受体。在雄性Sprague-Dawley大鼠(约300 g)中,将单侧右侧套管植入BLA和同侧NAc壳或核中。一周后,对大鼠进行了抑制回避(IA)任务的训练,并在48小时后对它们的保持力进行了测试。训练后立即将药物注入BLA和NAc外壳或核心。训练后在DA中进行BLA内输注可增强保留,如在保留测试中通过进入休克室的潜伏期评估。将通用DA受体拮抗剂顺式氟戊醇(Flu)注入NAc外壳(而不是核心)可阻止DA的BLA注入诱导的记忆增强。在反向实验中,训练后的DA的NAc内壳层输注增强了保留,而向BLA中注入了Flu则阻止了增强。这些发现表明,记忆整合的BLA调节需要同时在NAc外壳而非核心中激活DA受体。同样,记忆整合的NAc外壳调节需要同时激活BLA中的DA受体。与以前的发现一起,这些结果表明,BLA和NAc壳的多巴胺能神经支配与记忆整合的调节密切相关。

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