Replication study on the role of dopamine-dependent prefrontal reactivations in human extinction memory retrieval

Abstract Even after successful extinction, conditioned fear can return. Strengthening the consolidation of the fear-inhibitory safety memory formed during extinction is one way to counteract return of fear. In a previous study, we found that post-extinction L-DOPA administration improved extinction...

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Main Authors: Elena Andres, Hu Chuan-Peng, Anna M. V. Gerlicher, Benjamin Meyer, Oliver Tüscher, Raffael Kalisch
Format: Article
Language:English
Published: Nature Portfolio 2024-03-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-024-46936-y
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author Elena Andres
Hu Chuan-Peng
Anna M. V. Gerlicher
Benjamin Meyer
Oliver Tüscher
Raffael Kalisch
author_facet Elena Andres
Hu Chuan-Peng
Anna M. V. Gerlicher
Benjamin Meyer
Oliver Tüscher
Raffael Kalisch
author_sort Elena Andres
collection DOAJ
description Abstract Even after successful extinction, conditioned fear can return. Strengthening the consolidation of the fear-inhibitory safety memory formed during extinction is one way to counteract return of fear. In a previous study, we found that post-extinction L-DOPA administration improved extinction memory retrieval 24 h later. Furthermore, spontaneous post-extinction reactivations of a neural activation pattern evoked in the ventromedial prefrontal cortex (vmPFC) during extinction predicted extinction memory retrieval, L-DOPA increased the number of these reactivations, and this mediated the effect of L-DOPA on extinction memory retrieval. Here, we conducted a preregistered replication study of this work in healthy male participants. We confirm that spontaneous post-extinction vmPFC reactivations predict extinction memory retrieval. This predictive effect, however, was only observed 90 min after extinction, and was not statistically significant at 45 min as in the discovery study. In contrast to our previous study, we find no evidence that L-DOPA administration significantly enhances retrieval and that this is mediated by enhancement of the number of vmPFC reactivations. However, additional non-preregistered analyses reveal a beneficial effect of L-DOPA on extinction retrieval when controlling for the trait-like stable baseline levels of salivary alpha-amylase enzymatic activity. Further, trait salivary alpha-amylase negatively predicts retrieval, and this effect is reduced by L-DOPA treatment. Importantly, the latter findings result from non-preregistered analyses and thus further investigation is needed.
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spelling doaj.art-f0bf37484fd3478d84f1ccf5bff6591e2024-03-31T11:25:24ZengNature PortfolioNature Communications2041-17232024-03-0115111510.1038/s41467-024-46936-yReplication study on the role of dopamine-dependent prefrontal reactivations in human extinction memory retrievalElena Andres0Hu Chuan-Peng1Anna M. V. Gerlicher2Benjamin Meyer3Oliver Tüscher4Raffael Kalisch5Leibniz Institute for Resilience Research (LIR)Leibniz Institute for Resilience Research (LIR)Neuroimaging Center (NIC), Focus Program Translational Neuroscience (FTN), Johannes Gutenberg University Medical Center MainzLeibniz Institute for Resilience Research (LIR)Leibniz Institute for Resilience Research (LIR)Leibniz Institute for Resilience Research (LIR)Abstract Even after successful extinction, conditioned fear can return. Strengthening the consolidation of the fear-inhibitory safety memory formed during extinction is one way to counteract return of fear. In a previous study, we found that post-extinction L-DOPA administration improved extinction memory retrieval 24 h later. Furthermore, spontaneous post-extinction reactivations of a neural activation pattern evoked in the ventromedial prefrontal cortex (vmPFC) during extinction predicted extinction memory retrieval, L-DOPA increased the number of these reactivations, and this mediated the effect of L-DOPA on extinction memory retrieval. Here, we conducted a preregistered replication study of this work in healthy male participants. We confirm that spontaneous post-extinction vmPFC reactivations predict extinction memory retrieval. This predictive effect, however, was only observed 90 min after extinction, and was not statistically significant at 45 min as in the discovery study. In contrast to our previous study, we find no evidence that L-DOPA administration significantly enhances retrieval and that this is mediated by enhancement of the number of vmPFC reactivations. However, additional non-preregistered analyses reveal a beneficial effect of L-DOPA on extinction retrieval when controlling for the trait-like stable baseline levels of salivary alpha-amylase enzymatic activity. Further, trait salivary alpha-amylase negatively predicts retrieval, and this effect is reduced by L-DOPA treatment. Importantly, the latter findings result from non-preregistered analyses and thus further investigation is needed.https://doi.org/10.1038/s41467-024-46936-y
spellingShingle Elena Andres
Hu Chuan-Peng
Anna M. V. Gerlicher
Benjamin Meyer
Oliver Tüscher
Raffael Kalisch
Replication study on the role of dopamine-dependent prefrontal reactivations in human extinction memory retrieval
Nature Communications
title Replication study on the role of dopamine-dependent prefrontal reactivations in human extinction memory retrieval
title_full Replication study on the role of dopamine-dependent prefrontal reactivations in human extinction memory retrieval
title_fullStr Replication study on the role of dopamine-dependent prefrontal reactivations in human extinction memory retrieval
title_full_unstemmed Replication study on the role of dopamine-dependent prefrontal reactivations in human extinction memory retrieval
title_short Replication study on the role of dopamine-dependent prefrontal reactivations in human extinction memory retrieval
title_sort replication study on the role of dopamine dependent prefrontal reactivations in human extinction memory retrieval
url https://doi.org/10.1038/s41467-024-46936-y
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