首页> 外文期刊>Neurobiology of learning and memory >Region-specific roles of the prelimbic cortex, the dorsal CA1, the ventral DG and ventral CA1 of the hippocampus in the fear return evoked by a sub-conditioning procedure in rats
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Region-specific roles of the prelimbic cortex, the dorsal CA1, the ventral DG and ventral CA1 of the hippocampus in the fear return evoked by a sub-conditioning procedure in rats

机译:大鼠亚适应性程序诱发的恐惧返回中,前海皮质,海马背侧CA1,腹侧DG和腹侧CA1在区域特异性中的作用

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The return of learned fear is an important issue in anxiety disorder research since an analogous process may contribute to long-term fear maintenance or clinical relapse. A number of studies demonstrate that mPFC and hippocampus are important in the modulation of post-extinction re-expression of fear memory. However, the region-specific role of these structures in the fear return evoked by a sub-threshold conditioning (SC) is not known. In the present experiments, we first examined specific roles of the pre limbic cortex (PL), the dorsal hippocampus (DH, the dorsal CA1 area in particular), the ventral hippocampus (the ventral dentate gyrus (vDG) and the ventral CA1 area in particular) in this fear return process. Then we examined the role of connections between PL and vCA1 with this behavioral approach. Rats were subjected to five tone-shock pairings (1.0-mA shock) to induce conditioned fear (freezing), followed by three fear extinction sessions (25 tone-alone trials each session). After a post-test for extinction memory, some rats were retrained with the SC procedure to reinstate tone-evoked freezing. Rat groups were injected with low doses of the GABAA agonist muscimol to selectively inactivate PL, DH, vDG, or vCA1 120 min before the fear return test. A disconnection paradigm with ipsilateral or contralateral muscimol injection of the PL and the vCA1 was used to examine the role of this pathway in the fear return. We found that transient inactivation of these areas significantly impaired fear return (freezing): inactivation of the prelimbic cortex blocked SC-evoked fear return in particular but did not influence fear expression in general; inactivation of the DH area impaired fear return, but had no effect on the extinction retrieval process; both ventral DG and ventral CA1 are required for the return of extinguished fear whereas only ventral DG is required for the extinction retrieval. These findings suggest that PL, DH, vDG, and vCA1 all contribute to the fear return and connections between PL and vCA1 may be involved in the modulation of this process. (c) 2016 Elsevier Inc. All rights reserved.
机译:在焦虑症研究中,所学恐惧的回归是一个重要的问题,因为类似的过程可能有助于长期恐惧的维持或临床复发。大量研究表明,mPFC和海马在调节消亡后恐惧记忆的重新表达中起重要作用。但是,这些结构在特定阈值条件下引起的恐惧返回中的区域特定作用尚不清楚。在本实验中,我们首先检查了前缘皮质(PL),背侧海马区(DH,特别是背侧CA1区),腹侧海马区(腹侧齿状回(vDG)和腹侧CA1区的特定作用特别是在这种恐惧回归过程中。然后,我们使用这种行为方法研究了PL和vCA1之间的连接作用。对大鼠进行五次声震配对(1.0-mA冲击)以诱发条件性恐惧(冻结),然后进行三次恐惧消灭期(每期25次单音试验)。在进行灭绝记忆的后测后,对一些大鼠进行了SC程序再训练,以恢复音调诱发的冻结。在恐惧恐惧测试前120分钟,向大鼠组注射低剂量的GABAA激动剂麝香酚以选择性灭活PL,DH,vDG或vCA1。同侧或对侧麝香酚注射PL和vCA1的断开连接范例用于检查该途径在恐惧回归中的作用。我们发现这些区域的暂时失活严重损害了恐惧的返回(冻结):前肢皮层的失活尤其阻止了SC诱发的恐惧返回,但总体上不影响恐惧的表达。 DH区的失活削弱了恐惧的返回,但对灭绝恢复过程没有影响;消散恐惧的返回需要腹侧DG和腹侧CA1,而消退恢复只需要腹侧DG。这些发现表明,PL,DH,vDG和vCA1均会导致恐惧返回,并且PL和vCA1之间的连接可能参与了此过程的调节。 (c)2016 Elsevier Inc.保留所有权利。

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