Evidence map›Paper›PMID 42367984›Full record

ArticlebioRxiv : the preprint server for biology2026

DeltaQ: Value-Guided Hebbian Learning in Spiking Neuronal Networks for Multi-Goal Navigation.

Christopher Earl, Gozde Unal, Hananel Hazan, Samuel A Neymotin

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Christopher EarlOkinawa Institute of Science and Technology, Okinawa, Japan.
Gozde UnalCenter for Biomedical Imaging and Neuromodulation, Nathan Kline Institute for Psychiatric Research Orangeburg, NY.
Hananel HazanAllen Discovery Center, Tufts University, Medford, MA.ORCID 0000-0003-1446-1628
Samuel A NeymotinCenter for Biomedical Imaging and Neuromodulation, Nathan Kline Institute for Psychiatric Research Orangeburg, NY.ORCID 0000-0003-3646-5195

Funding

Project 5: ComputationalP50MH109429 · NIMH · NATHAN S. KLINE INSTITUTE FOR PSYCH RES · PI Michael Peter Milham · 2017 to 2026
$25.3M
Cortical and thalamic mechanisms of selective auditory attentionR01DC012947 · NIDCD · NATHAN S. KLINE INSTITUTE FOR PSYCH RES · PI NEYMOTIN, SAMUEL A, SCHROEDER, CHARLES E · 2013 to 2022
$5.2M
Dynamic circuit motifs underlying multimodal interactions in primate auditory cortexR01DC019979 · NIDCD · NATHAN S. KLINE INSTITUTE FOR PSYCH RES · PI Stephan Bickel, Samuel A Neymotin · 2022 to 2026
$3.3M
Auditory event-related potentials as in vivo preclinical assays of circuit engagement for E/I-based therapeutic developmentR01MH134118 · NIMH · NATHAN S. KLINE INSTITUTE FOR PSYCH RES · PI JAVITT, DANIEL C., NEYMOTIN, SAMUEL A · 2023 to 2024
$1.6M
NIDCD NIH HHS R01 DC012947NIDCD NIH HHS R01 DC019979NIMH NIH HHS P50 MH109429NIMH NIH HHS R01 MH134118
6 · The paper itself

Abstract

Animals must often navigate environments where feedback about progress toward a goal is sparse or delayed, requiring internal representations of space and memory of prior experience. The hippocampal-entorhinal system is believed to support this capability through distributed spatial representations that guide goal-directed behavior. However, many computational models of these circuits focus primarily on reproducing neural dynamics rather than demonstrating how such representations support learning on navigation tasks. We present a biologically inspired spiking neuronal network (SNN) model that combines grid-cell-derived spatial representations, ΔQ-modulated Hebbian plasticity, and context-dependent modulation to support navigation under sparse reward conditions. Grid Cell populations generate distributed spatial codes that are transformed by an Association Cell population into more spatially selective internal representations. Learning is driven by changes in Q-values (ΔQ) computed from a goal-conditioned Q-table, allowing local synaptic plasticity to incorporate information about long-term navigation outcomes. For environments containing multiple navigation objectives, a Context Cell population provides task-dependent modulation that enables a shared network architecture to support distinct navigation policies. Across two complementary maze environments, the model demonstrates three core capabilities: generation of distinct spatial representations, learning of efficient navigation policies under sparse and delayed reward, and support for multiple navigation objectives within a shared environment. The results further show that contextual modulation introduces subtle task-dependent variations into a largely shared population representation, allowing identical spatial locations to support different navigation behaviors. These findings demonstrate that biologically inspired spatial representations, value-guided plasticity, and contextual modulation can jointly support flexible navigation in spiking neuronal networks, providing a bridge between mechanistic neural circuit models and functional reinforcement learning.

Identifiers

PMID42367984
PMCPMC13308139

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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 Socratic graph.