Evidence map›Paper›PMID 41092900›Full record

ArticleCurrent biology : CB2025

Short-term memory by distributed neural network oscillators in a simple nervous system.

Raymond L Dunn, Caitriona M Costello, Jackson M Borchardt, Daniel Y Sprague, Grace C Chiu, Julia M Miller, Noelle D L'Etoile, Saul Kato

Abstract read
In one paragraph

Article in Current biology : CB, 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

5 · Who and what money

Authors and funding

8 authors.

Raymond L DunnWeill Institute of Neurosciences, University of California, San Francisco, San Francisco, CA 94158, USA.
Caitriona M CostelloWeill Institute of Neurosciences, University of California, San Francisco, San Francisco, CA 94158, USA.
Jackson M BorchardtWeill Institute of Neurosciences, University of California, San Francisco, San Francisco, CA 94158, USA.
Daniel Y SpragueWeill Institute of Neurosciences, University of California, San Francisco, San Francisco, CA 94158, USA.
Grace C ChiuWeill Institute of Neurosciences, University of California, San Francisco, San Francisco, CA 94158, USA.
Julia M MillerDepartment of Cell and Tissue Biology, University of California, San Francisco, San Francisco, CA 94143, USA.
Noelle D L'EtoileDepartment of Cell and Tissue Biology, University of California, San Francisco, San Francisco, CA 94143, USA.
Saul KatoWeill Institute of Neurosciences, University of California, San Francisco, San Francisco, CA 94158, USA. Electronic address: saul.kato@ucsf.edu.

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Aric L Daul, Ann E. Rougvie · 2012 to 2026
$7.5M
Olfactory memory acquisition consolidation and recallR01DC005991 · NIDCD · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI L 'ETOILE, NOELLE D · 2005 to 2022
$7.1M
The Effects of Stimulation and Sleep on Neural Circuit ConnectionsR01NS087544 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Noelle D L 'Etoile, Miri Kerensa VanHoven · 2014 to 2026
$6.2M
Emergence of Functional Network Dynamics from Single Cell PropertiesR35GM124735 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KATO, SAUL S · 2017 to 2021
$1.9M
Closed-loop control of neural dynamics and action selection in C elegansF31NS115572 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI DUNN, RAYMOND LAKE · 2019 to 2021
$124k
NIDCD NIH HHS R01 DC005991NIGMS NIH HHS R35 GM124735NIH HHS P40 OD010440NINDS NIH HHS F31 NS115572NINDS NIH HHS R01 NS087544
6 · The paper itself

Abstract

Short-term memory allows an animal to gather sensory evidence over time, integrate it with evolving internal state, and make informed decisions about when and how to act at a later time. The implementation of short-term memory by brains remains an outstanding mystery. Simpler animals such as the microscopic nematode C. elegans present the opportunity to understand, at a deep mechanistic level, how cognitive functions such as short-term memory are implemented by biological neural networks. We first establish that C. elegans can remember recent sensory experience to make discrete, informed turns for chemotaxis. Then, using a closed-loop virtual-reality system combining whole-brain imaging and targeted optogenetic neural perturbation, we find that this memory is held in the relative phase of the distributed oscillations of two groups of many neurons. One oscillatory neural complex drives the sequence of well-defined behavioral command states of the animal, and the other oscillatory neural complex drives large swings of the animal's head during forward crawling. However, during reverse crawling, the headswing oscillatory complex, in coordination with the command state complex, serves as a phase-based memory system. We propose that the implementation of a short-term memory system via the internalization of motor oscillations could represent the evolutionary origin of flexible internal neural network processing, i.e., thought, and a foundation of higher cognition.

Indexed as

Caenorhabditis elegansMemory, Short-TermNerve NetAnimalsBrainChemotaxisNeuronsOptogeneticsbrain oscillationsC. elegansclosed loopcognitiondecision-makingneural dynamicsneural manifoldoptogeneticsshort-term memorywhole-brain imaging

Identifiers

PMID41092900
PMCPMC12829590

What OpenQuestion holds

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Registered trials

None linked

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.