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检索后抑制磷酸二酯酶 4 会改变记忆命运,有利于遗忘而不是再巩固。

Phosphodiesterase 4 inhibition after retrieval switches the memory fate favoring extinction instead of reconsolidation.

机构信息

Department of Pharmacology, Federal University of Parana, Curitiba, PR, Brazil.

Department of Psychiatry and Neuropsychology, School of Mental Health and Neuroscience, University of Maastricht, Maastricht, The Netherlands.

出版信息

Sci Rep. 2023 Nov 21;13(1):20384. doi: 10.1038/s41598-023-47717-1.

Abstract

Phosphodiesterase 4 (PDE4), an enzyme expressed in the dorsal hippocampus (DH), hydrolyzes the cAMP, limiting the PKA-induced CREB phosphorylation (pCREB) and BDNF expression. Depending on the brain region, PKA and pCREB mediate reconsolidation or extinction, whereas BDNF is mainly related to extinction facilitation. The mechanisms underpinning the switch between reconsolidation and extinction are relatively unknown. Here, we tested the hypothesis that PDE4 might control these processes. We showed in Wistar rats submitted to contextual fear conditioning that PDE4 inhibition with roflumilast (ROF) within the DH, after a short retrieval, did not change freezing behavior after one day (TestA). After 10 days, the ROF-treated group significantly reduced the expression of freezing behavior. This effect depended on retrieval, Test A exposure, and reinstated after a remainder foot shock, suggesting an extinction facilitation. The ROF effect depended on PKA after retrieval or, protein synthesis after Test A. After retrieval, ROF treatment did not change the pCREB/CREB ratio in the DH. It enhanced proBDNF expression without changing pre-proBDNF or mature BDNF in the DH after Test A. The results suggest that the inhibition of PDE4 in the DH after a short retrieval changes the memory sensibility from reconsolidation to extinction via regulating proBDNF expression.

摘要

磷酸二酯酶 4(PDE4)是一种在背侧海马(DH)中表达的酶,可水解 cAMP,限制 PKA 诱导的 CREB 磷酸化(pCREB)和 BDNF 表达。根据大脑区域的不同,PKA 和 pCREB 介导再巩固或遗忘,而 BDNF 主要与遗忘促进有关。再巩固和遗忘之间转换的机制尚不清楚。在这里,我们检验了 PDE4 可能控制这些过程的假设。我们在接受情境性恐惧条件反射的 Wistar 大鼠中表明,在短时间检索后,DH 中的罗氟司特(ROF)抑制 PDE4 不会改变一天后的冻结行为(TestA)。10 天后,ROF 处理组显著减少了冻结行为的表达。这种作用取决于检索、Test A 暴露和再刺激后的剩余足部电击,提示遗忘促进。ROF 的作用取决于检索后的 PKA 或 Test A 后的蛋白质合成。检索后,ROF 处理不会改变 DH 中的 pCREB/CREB 比值。它增强了 proBDNF 的表达,而在 Test A 后,DH 中的 pre-proBDNF 或成熟 BDNF 没有改变。结果表明,短时间检索后 DH 中 PDE4 的抑制通过调节 proBDNF 的表达,将记忆敏感性从再巩固转变为遗忘。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb09/10663466/242db5d9b445/41598_2023_47717_Fig1_HTML.jpg

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