Memory erasure by dopamine-gated retrospective learning

Erasing outdated memories is crucial for adaptive behavior. Yet once a cue-outcome association is learned, repeated cue exposure without outcome suppresses conditioned behavior without erasing the underlying memory. This allows rapid behavioral recovery when outcomes are reintroduced. Here, we confirm this limitation for standard "prospective extinction" protocols that present cues without the associated outcome, but show that true memory erasure is achieved by inverting the paradigm: presenting outcomes without associated cues, i.e., "retrospective extinction". We demonstrate that orbitofrontal cortex activity at outcome is necessary for the rapid behavioral recovery following prospective extinction, and that mesolimbic dopamine activity at outcome is necessary for retrospective extinction. These findings reconceptualize extinction mechanisms and suggest complementary strategies to mitigate relapse and erase maladaptive memories.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-01-21
DOI
https://doi.org/10.64898/2026.01.17.700100
Primary Topic
Memory and Neural Mechanisms
Type
article
Field-Weighted Citation Impact
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article

Memory erasure by dopamine-gated retrospective learning

Leo Zsembik, Styra Xicun Wang, Ritchie Chen, Sara Brooke et al.
bioRxiv (Cold Spring Harbor Laboratory)
Memory and Neural Mechanisms
article

Memory erasure by dopamine-gated retrospective learning

Leo Zsembik, Styra Xicun Wang, Ritchie Chen, Sara Brooke, Vijay Mohan K Namboodiri, Eric Garr, Huijeong Jeong, Mingkang Zhou, Marco Leyton, Sylvia M. L. Cox, Farah Farouq, Risha Chakraborty, Andrea D. Sanders, Ananya Srinivasan, Nishita Belur, Patricia H. Janak
article en

Abstract

Erasing outdated memories is crucial for adaptive behavior. Yet once a cue-outcome association is learned, repeated cue exposure without outcome suppresses conditioned behavior without erasing the underlying memory. This allows rapid behavioral recovery when outcomes are reintroduced. Here, we confirm this limitation for standard "prospective extinction" protocols that present cues without the associated outcome, but show that true memory erasure is achieved by inverting the paradigm: presenting outcomes without associated cues, i.e., "retrospective extinction". We demonstrate that orbitofrontal cortex activity at outcome is necessary for the rapid behavioral recovery following prospective extinction, and that mesolimbic dopamine activity at outcome is necessary for retrospective extinction. These findings reconceptualize extinction mechanisms and suggest complementary strategies to mitigate relapse and erase maladaptive memories.

bioRxiv (Cold Spring Harbor Laboratory)
Johns Hopkins University (US), University of California, San Francisco (US), Johns Hopkins Medicine (US), Yale University (US), Center for Neurosciences (US), Neurological Surgery (US), McGill University (CA), University of California, Berkeley (US)
Openalex Percentile: Top 82%
Memory and Neural Mechanisms
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