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Glucocorticoid-cholinergic interactions in the dorsal striatum in memory consolidation of inhibitory avoidance training

机译:背侧纹状体中糖皮质激素-胆碱能相互作用在抑制回避训练记忆巩固中的作用

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摘要

Extensive evidence indicates that glucocorticoid hormones act in a variety of brain regions to enhance the consolidation of memory of emotionally motivated training experiences. We previously reported that corticosterone, the major glucocorticoid in the rat, administered into the dorsal striatum immediately after inhibitory avoidance training dose-dependently enhances memory consolidation of this training. There is also abundant evidence that the intrinsic cholinergic system of the dorsal striatum is importantly involved in memory consolidation of inhibitory avoidance training. However, it is presently unknown whether these two neuromodulatory systems interact within the dorsal striatum in the formation of long-term memory. To address this issue, we first investigated in male Wistar rats whether the muscarinic receptor agonist oxotremorine administered into the dorsal striatum immediately after inhibitory avoidance training enhances 48 h retention of the training. Subsequently, we examined whether an attenuation of glucocorticoid signaling by either a systemic administration of the corticosterone-synthesis inhibitor metyrapone or an intra-striatal infusion of the glucocorticoid receptor (GR) antagonist RU 38486 would block the memory enhancement induced by oxotremorine. Our findings indicate that oxotremorine dose-dependently enhanced 48 h retention latencies, but that the administration of either metyrapone or RU 38486 prevented the memory-enhancing effect of oxotremorine. In the last experiment, corticosterone was infused into the dorsal striatum together with the muscarinic receptor antagonist scopolamine immediately after inhibitory avoidance training. Scopolamine blocked the enhancing effect of corticosterone on 48 h retention performance. These findings indicate that there are mutual interactions between glucocorticoids and the striatal cholinergic system in enhancing the consolidation of memory of inhibitory avoidance training.
机译:大量证据表明,糖皮质激素可在大脑的各个区域发挥作用,以增强对情感动机的训练记忆的记忆。我们先前曾报道,抑制性避免训练后,立即将皮质酮(大鼠中的主要糖皮质激素)施用于背部纹状体,可剂量依赖性地增强该训练的记忆巩固。也有大量证据表明,背侧纹状体的内在胆碱能系统与抑制回避训练的记忆巩固有关。然而,目前尚不清楚这两个神经调节系统是否在长期纹状体的背侧纹状体内相互作用。为了解决这个问题,我们首先在雄性Wistar大鼠中研究了抑制回避训练后立即向背侧纹状体施用毒蕈碱受体激动剂oxotremorine是否会增加训练的48 h保留时间。随后,我们研究了通过全身性给予皮质酮合成抑制剂甲吡酮或纹状体内输注糖皮质激素受体(GR)拮抗剂RU 38486所引起的糖皮质激素信号传导的减弱是否会阻断由oxotremorine引起的记忆增强。我们的发现表明,oxotremorine剂量依赖性地增加了48 h的保留潜伏期,但甲吡酮或RU 38486的给药阻止了oxotremorine的记忆增强作用。在最后一个实验中,抑制性回避训练后,立即将皮质酮与毒蕈碱受体拮抗剂东pol碱一起注入到背侧纹状体中。东co碱阻断了皮质酮对48小时保留性能的增强作用。这些发现表明,糖皮质激素和纹状体胆碱能系统之间存在相互作用,从而增强了抑制回避训练记忆的巩固。

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