Evidence map›Paper›PMID 41398471›Full record

ArticleCommunications biology2025

Low-dimensional signatures of neuronal activity associated with long-term operant conditioning in Aplysia.

Sara Vanaki, Nicholas O Gonzalez, Curtis L Neveu, Yuto Momohara, Behnaam Aazhang, John H Byrne

Abstract read
In one paragraph

Article in Communications biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Sara Vanaki *Department of Neurobiology and Anatomy, W.M. Keck Center for the Neurobiology of Learning and Memory, McGovern Medical School at the University of Texas Health Science Center, Houston, TX, USA.ORCID http://orcid.org/0009-0001-3062-7897
Nicholas O Gonzalez *Department of Neurobiology and Anatomy, W.M. Keck Center for the Neurobiology of Learning and Memory, McGovern Medical School at the University of Texas Health Science Center, Houston, TX, USA.
Curtis L NeveuDepartment of Neurobiology and Anatomy, W.M. Keck Center for the Neurobiology of Learning and Memory, McGovern Medical School at the University of Texas Health Science Center, Houston, TX, USA.
Yuto MomoharaDepartment of Neurobiology and Anatomy, W.M. Keck Center for the Neurobiology of Learning and Memory, McGovern Medical School at the University of Texas Health Science Center, Houston, TX, USA.
Behnaam AazhangDepartment of Electrical and Computer Engineering, Rice University, Houston, TX, USA.
John H ByrneDepartment of Neurobiology and Anatomy, W.M. Keck Center for the Neurobiology of Learning and Memory, McGovern Medical School at the University of Texas Health Science Center, Houston, TX, USA. John.H.Byrne@uth.tmc.edu.ORCID http://orcid.org/0000-0001-7947-5890

Funding

Analyses of the Distributed Representation of Associative-Learning in an Identified Circuit Using a Combination of Single-Cell Electrophysiology and Multicellular Voltage-Sensitive Dye RecordingsR01NS101356 · NINDS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI John H Byrne · 2018 to 2026
$3.2M
NINDS NIH HHS R01 NS101356U.S. Department of Health & Human Services | NIH | National Institute of Neurological Disorders and Stroke (NINDS) NS101356
6 · The paper itself

Abstract

Operant conditioning is a form of learning in which a behavior is reinforced by reward. Operant conditioning has multiple temporal domains, ranging from short-term, lasting a few minutes, to long-term, persisting for at least 24 h. The extent to which short- and long-term operant conditioning memories rely on shared or separate neural mechanisms is poorly understood. Voltage-sensitive dye (VSD) imaging has been used previously to record the activity of a large number of neurons simultaneously in the buccal ganglion to measure changes in neuronal activity during short-term operant conditioning. We examined neuronal activity using VSD 24 h after operant conditioning and compared these results with those from short-term operant conditioning to assess the extent to which short-term and long-term operant conditioning share common neural correlates. Non-negative matrix factorization (NMF) isolated the temporal signature of neuronal activity. Similar to short-term operant conditioning, long-term operant conditioning resulted in an earlier recruitment of an NMF module that corresponded to the retraction phase of feeding behavior, which indicated that the temporal signatures of short- and long-term operant conditioning share similar features. In contrast to short-term operant conditioning, long-term operant conditioning engaged a larger population of retraction neurons in a region of the buccal ganglion containing sensory neurons. These findings suggest that a more extensive network is involved in long-term operant conditioning memory.

Indexed as

AplysiaConditioning, OperantNeuronsAnimalsVoltage-Sensitive Dye Imaging

Identifiers

PMID41398471
PMCPMC12820046

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.