Evidence map›Paper›PMID 41279929›Full record

ArticlebioRxiv : the preprint server for biology2025

Effective computations for hippocampal place cell phenomena in sparse untrained random networks.

José R Hurtado, SueYeon Chung, André A Fenton

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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

3 authors.

José R HurtadoNew York University.
SueYeon ChungHarvard University.
André A FentonNew York University.ORCID 0000-0002-5063-1156

Funding

Towards a critical test of the synaptic plasticity and memory hypothesisR01MH132204 · NIMH · NEW YORK UNIVERSITY · PI ANDRE ANTONIO FENTON · 2023 to 2026
$2.5M
NIMH NIH HHS R01 MH132204
6 · The paper itself

Abstract

The mammalian brain processes experience-dependent spatial information through poorly-understood network mechanisms thought to depend on particular network connectivity patterns and activity-dependent synaptic plasticity. However, dedicated input connections that learn to shape information about place cannot easily explain many rodent hippocampal place cell phenomena. For example, representational drift notwithstanding, the discharge of each place cell maps to specific locations in a fixed environment, but the discharge of most cells remap to distinct independent locations across environments, despite the fact that most sub-second cofiring relationships amongst hippocampal neuron pairs persist across environments. Whereas some models of hippocampal spatial information processing rely on the dedicated input connections of a for-purpose connectome (ignoring remapping, representational drift, and maintained cofiring), other models use synaptic plasticity implemented by learning rules to alter random input connections, but struggle with either limited capacity, representational drift, and/or biological implausibility. Here, using a randomly tuned network with feedback inhibition, we examine whether the assumptions of a specific connectome and learning-implemented synaptic plasticity are necessary for diverse place cell phenomena. We find that the random network with non-plastic connections accounts for positional tuning, single place fields in small spaces and multiple place fields in large spaces, mixed selectivity, and remapping, amongst other place cell phenomena. This requires excitatory activity to be sparse and organized across stimuli by divisive normalization. Enabling synaptic plasticity only at the network connections (not at network inputs) accounts for additional place cell phenomena including overdispersion, representational drift, and memory tagging. We show by simulations and analytically that DivSparse, a random network with sparsifying inhibition can explain many features of place cell network activity, suggesting that simple biologically-plausible architectures can realize representations of spatial experience that are robust, flexible, and spontaneous.

Identifiers

PMID41279929
PMCPMC12632505

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.