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内侧海马微量注射 D-环丝氨酸对大鼠恐惧性消退的影响,以及 NMDA 受体亚单位 NR2B 和海马神经发生的表达。

The effects of intra-hippocampal microinfusion of D-cycloserine on fear extinction, and the expression of NMDA receptor subunit NR2B and neurogenesis in the hippocampus in rats.

机构信息

Department of Psychiatry, The First Hospital of China Medical University, Shenyang, 110001, PR China.

出版信息

Prog Neuropsychopharmacol Biol Psychiatry. 2013 Jul 1;44:257-64. doi: 10.1016/j.pnpbp.2013.02.017. Epub 2013 Mar 21.

Abstract

Pharmacological and behavior interventions for inhibiting fear and anxiety are important in the treatment of different types of anxiety disorder. Fear extinction, as a novel form of associative learning, is the most extensively studied models to understand the neural mechanisms of fear-related and anxiety disorders. One of the possible mechanisms of neural plasticity in extinction learning may depend on activation of NMDA receptors in the amygdale; however, the role played by the hippocampus in extinction remains largely unclear. In the present study, using a fear conditioning paradigm, we repeatedly microinfused D-cycloserine, a partial agonist of NMDA receptor, into the hippocampus and investigated the effects of repeated infusions of DCS on extinction behavior and protein levels of NMDA receptor subunit NR2B. We also examined the effects of DCS on neurogenesis in adult rat hippocampus. Our results showed that the administration of DCS facilitated the acquisition and retrieval of extinction memory, and enhanced the expression of NR2B protein in the dentate gyrus, CA1 and CA3 of the hippocampus. We also found that repeated microinfusions of DCS increased proliferation of newly born cells in the hippocampus. These findings suggest that neural plasticity mediated by NMDA receptors in the hippocampus is involved in the enhancement of acquisition and retrieval of extinction memory.

摘要

药理学和行为干预措施对于抑制恐惧和焦虑在治疗不同类型的焦虑症中非常重要。作为一种新的联想学习形式,恐惧消退是研究恐惧相关和焦虑障碍神经机制的最广泛的模型之一。在消退学习中神经可塑性的一种可能机制可能取决于杏仁核中 NMDA 受体的激活;然而,海马在消退中的作用在很大程度上仍不清楚。在本研究中,我们使用恐惧条件反射范式,反复将 NMDA 受体部分激动剂 D-环丝氨酸微注入海马体,并研究了 DCS 的重复输注对消退行为和 NMDA 受体亚单位 NR2B 蛋白水平的影响。我们还研究了 DCS 对成年大鼠海马体神经发生的影响。我们的结果表明,DCS 的给药促进了消退记忆的获得和检索,并增强了海马体齿状回、CA1 和 CA3 中 NR2B 蛋白的表达。我们还发现,DCS 的重复微注射增加了海马中新生成细胞的增殖。这些发现表明,海马体中 NMDA 受体介导的神经可塑性参与了消退记忆获得和检索的增强。

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