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恐惧再激活激活齿状回中的环磷酸腺苷信号通路。

Fear renewal activates cyclic adenosine monophosphate signaling in the dentate gyrus.

机构信息

Faculty of Forensic Medicine, Zhongshan School of Medicine, Sun Yat-Sen University, Guangzhou, China.

Guangdong Province Key Laboratory of Brain Function and Disease, Zhongshan School of Medicine, Sun Yat-Sen University, Guangzhou, China.

出版信息

Brain Behav. 2019 Aug;9(8):e01280. doi: 10.1002/brb3.1280. Epub 2019 Jul 17.

Abstract

BACKGROUND

Fear renewal, the context-specific relapse of a conditioned fear after extinction, is a widely pursued model of post-traumatic stress disorder and phobias. However, its cellular and molecular mechanisms remain poorly understood. The dentate gyrus (DG) has emerged as a critical locus of plasticity with relevance to memory, anxiety disorders, and depression, and it contributes to fear memory retrieval. Here, we have identified the role of the DG in fear renewal and its molecular mechanism.

MATERIALS AND METHODS

Muscimol (MUS), activator of cyclic adenosine monophosphate (cAMP) forskolin (FSK), inhibitor of protein kinase A (PKA), Rip-cAMP, and a phosphodiesterase inhibitor rolipram were infused into DG of standard deviation rats before renewal testing. cAMP levels after fear renewal was measured by enzyme-linked immunosorbent assay. The protein levels of phosphodiesterase 4 (PDE4) isoforms were tested by western blot. At last, the roles of cAMP signaling were also tested in the acquisition of fear conditioning, fear retrieval, and extinction.

RESULTS

Intra-DG treatment of MUS and Rp-cAMP impaired fear renewal. FSK and rolipram exhibited the opposite effect, which also occurred in the retrieval of original fear memory. This change in fear renewal was regulated by PDE4 isoforms PDE4A, PDE4A5, and PDE4D. In addition, FSK and rolipram facilitated the acquisition of fear conditioning in long-term memory, but not short-term memory, while Rp-cAMP impaired long-term memory. For extinction, FSK and rolipram inhibited extinction process, while Rp-cAMP facilitated fear extinction.

CONCLUSION

These findings demonstrated that fear renewal activated cAMP signaling in the DG through decreased PDE4 activity. Because of the role of cAMP signaling in the acquisition or retrieval of fear conditioning and encoding of extinction, it is speculated that initial learning and extinction may have similarities in molecular mechanism, especially fear retrieval and fear renewal may share cAMP signaling pathway in the DG.

摘要

背景

恐惧再现是指在消退后条件性恐惧的特定情境复发,是创伤后应激障碍和恐惧症的广泛研究模型。然而,其细胞和分子机制仍知之甚少。齿状回(DG)作为与记忆、焦虑障碍和抑郁相关的可塑性关键部位,并有助于恐惧记忆的检索。在这里,我们确定了 DG 在恐惧再现中的作用及其分子机制。

材料和方法

在再测试前,将 muscimol (MUS)、环磷酸腺苷 (cAMP) 佛司可林 (FSK) 的激活剂、蛋白激酶 A (PKA) 的抑制剂 Rip-cAMP 和磷酸二酯酶抑制剂 rolipram 输注到标准偏差大鼠的 DG 中。通过酶联免疫吸附试验测量恐惧再现后 cAMP 水平。通过蛋白质印迹测试磷酸二酯酶 4 (PDE4) 同工型的蛋白水平。最后,还测试了 cAMP 信号在恐惧条件反射的获得、恐惧检索和消退中的作用。

结果

DG 内注射 MUS 和 Rp-cAMP 可损害恐惧再现。FSK 和 rolipram 表现出相反的效果,这也发生在原始恐惧记忆的检索中。恐惧再现的这种变化受 PDE4 同工型 PDE4A、PDE4A5 和 PDE4D 调节。此外,FSK 和 rolipram 促进了长时记忆中恐惧条件反射的获得,但不促进短时记忆,而 Rp-cAMP 损害了长时记忆。对于消退,FSK 和 rolipram 抑制了消退过程,而 Rp-cAMP 促进了恐惧消退。

结论

这些发现表明,DG 中的恐惧再现通过降低 PDE4 活性激活了 cAMP 信号。由于 cAMP 信号在恐惧条件反射的获得或检索以及消退的编码中的作用,推测初始学习和消退在分子机制上可能具有相似性,特别是恐惧检索和恐惧再现可能在 DG 中共享 cAMP 信号通路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5fd8/6710207/6a889dc2f441/BRB3-9-e01280-g001.jpg

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