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Phosphodiesterase 4 inhibition after retrieval switches the memory fate favoring extinction instead of reconsolidation
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 extinc...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10663466/ https://www.ncbi.nlm.nih.gov/pubmed/37990053 http://dx.doi.org/10.1038/s41598-023-47717-1 |
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author | Machado Batista Sohn, Jeferson Cardoso, Nathalie Carla Raymundi, Ana Maria Prickaerts, Jos Stern, Cristina Aparecida Jark |
author_facet | Machado Batista Sohn, Jeferson Cardoso, Nathalie Carla Raymundi, Ana Maria Prickaerts, Jos Stern, Cristina Aparecida Jark |
author_sort | Machado Batista Sohn, Jeferson |
collection | PubMed |
description | 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(1)). After 10 days, the ROF-treated group significantly reduced the expression of freezing behavior. This effect depended on retrieval, Test A(1) 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(1). 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(1). 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. |
format | Online Article Text |
id | pubmed-10663466 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-106634662023-11-21 Phosphodiesterase 4 inhibition after retrieval switches the memory fate favoring extinction instead of reconsolidation Machado Batista Sohn, Jeferson Cardoso, Nathalie Carla Raymundi, Ana Maria Prickaerts, Jos Stern, Cristina Aparecida Jark Sci Rep Article 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(1)). After 10 days, the ROF-treated group significantly reduced the expression of freezing behavior. This effect depended on retrieval, Test A(1) 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(1). 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(1). 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. Nature Publishing Group UK 2023-11-21 /pmc/articles/PMC10663466/ /pubmed/37990053 http://dx.doi.org/10.1038/s41598-023-47717-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Machado Batista Sohn, Jeferson Cardoso, Nathalie Carla Raymundi, Ana Maria Prickaerts, Jos Stern, Cristina Aparecida Jark Phosphodiesterase 4 inhibition after retrieval switches the memory fate favoring extinction instead of reconsolidation |
title | Phosphodiesterase 4 inhibition after retrieval switches the memory fate favoring extinction instead of reconsolidation |
title_full | Phosphodiesterase 4 inhibition after retrieval switches the memory fate favoring extinction instead of reconsolidation |
title_fullStr | Phosphodiesterase 4 inhibition after retrieval switches the memory fate favoring extinction instead of reconsolidation |
title_full_unstemmed | Phosphodiesterase 4 inhibition after retrieval switches the memory fate favoring extinction instead of reconsolidation |
title_short | Phosphodiesterase 4 inhibition after retrieval switches the memory fate favoring extinction instead of reconsolidation |
title_sort | phosphodiesterase 4 inhibition after retrieval switches the memory fate favoring extinction instead of reconsolidation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10663466/ https://www.ncbi.nlm.nih.gov/pubmed/37990053 http://dx.doi.org/10.1038/s41598-023-47717-1 |
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