Evidence map›Paper›PMID 39657670›Full record

ArticleCurrent biology : CB2025

Origin of visual experience-dependent theta oscillations.

Michael P Zimmerman, Samuel T Kissinger, Paige Edens, Renee C Towers, Sanghamitra Nareddula, Yididiya Y Nadew, Christopher J Quinn, Alexander A Chubykin

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 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

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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

8 authors.

Michael P ZimmermanDepartment of Biological Sciences, Purdue Institute for Integrative Neuroscience, Purdue University, 915 Mitch Daniels Blvd., West Lafayette, IN 47907, USA; Department of Biomedical Engineering, Purdue University, 206 S. Martin Jischke Dr., West Lafayette, IN 47907, USA.
Samuel T KissingerDepartment of Biological Sciences, Purdue Institute for Integrative Neuroscience, Purdue University, 915 Mitch Daniels Blvd., West Lafayette, IN 47907, USA.
Paige EdensDepartment of Biological Sciences, Purdue Institute for Integrative Neuroscience, Purdue University, 915 Mitch Daniels Blvd., West Lafayette, IN 47907, USA.
Renee C TowersDepartment of Biological Sciences, Purdue Institute for Integrative Neuroscience, Purdue University, 915 Mitch Daniels Blvd., West Lafayette, IN 47907, USA.
Sanghamitra NareddulaDepartment of Biological Sciences, Purdue Institute for Integrative Neuroscience, Purdue University, 915 Mitch Daniels Blvd., West Lafayette, IN 47907, USA.
Yididiya Y NadewDepartment of Computer Sciences, Iowa State University, 2434 Osborn Dr., Ames, IA 50011, USA.
Christopher J QuinnDepartment of Computer Sciences, Iowa State University, 2434 Osborn Dr., Ames, IA 50011, USA.
Alexander A ChubykinDepartment of Biological Sciences, Purdue Institute for Integrative Neuroscience, Purdue University, 915 Mitch Daniels Blvd., West Lafayette, IN 47907, USA. Electronic address: chubykin@purdue.edu.

Funding

Neural Mechanisms of Predictive Impairments in AutismR01MH116500 · NIMH · PURDUE UNIVERSITY · PI Alexander Chubykin · 2017 to 2026
$3.8M
NIMH NIH HHS R01 MH116500
6 · The paper itself

Abstract

Visual experience gives rise to persistent theta oscillations in the mouse primary visual cortex (V1) that are specific to the familiar stimulus. Our recent work demonstrated the presence of these oscillations in higher visual areas (HVAs), where they are synchronized with V1 in a context-dependent manner. However, it remains unclear where these unique oscillatory dynamics originate. To investigate this, we conducted paired extracellular electrophysiological recordings in two visual thalamic nuclei (dorsal lateral geniculate nucleus [dLGN] and lateral posterior nucleus [LP]), the retrosplenial cortex (RSC), and the hippocampus (HPC). Oscillatory activity was not found in either of the thalamic nuclei, but a sparse ensemble of oscillating neurons was observed in both the RSC and HPC, similar to V1. To infer functional connectivity changes between the brain regions, we performed directed information analysis, which indicated a trend toward decreased connectivity in all V1-paired regions, with a consistent increase in V1 → V1 connections, suggesting that the oscillations appear to initiate independently within V1. Lastly, complete NMDA lesioning of the HPC did not abolish theta oscillations in V1 that emerge with familiarity. Altogether, these results suggest that (1) theta oscillations do not originate in the thalamus; (2) RSC exhibits theta oscillations, which may follow V1 given the temporal delay present; and (3) the HPC had a sparse group of neurons, with theta oscillations matching V1; however, lesioning suggests that these oscillations emerge independent of each other. Overall, our findings pave the way for future studies to determine the mechanisms by which diverse inputs and outputs shape this memory-related oscillatory activity in the brain.

Indexed as

Theta RhythmAnimalsHippocampusMaleMiceMice, Inbred C57BLNeuronsPrimary Visual CortexVisual CortexVisual PathwaysVisual Perceptionfamiliaritylearningmemoryoscillationsilicon probesthetavisual cortex

Identifiers

PMID39657670
PMCPMC11720618

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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.