Evidence map›Paper›PMID 39476952›Full record

ArticleBrain stimulation

Concurrent optogenetic motor mapping of multiple limbs in awake mice reveals cortical organization of coordinated movements.

Nischal Khanal, Jonah A Padawer-Curry, Trevor Voss, Kevin A Schulte, Annie R Bice, Adam Q Bauer

Abstract read
In one paragraph

Article in Brain stimulation. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Action-type mapping principles extend beyond evolutionarily conserved actions, even in people born without hands.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  5. Multi-coil TMS for preclinical applications in ultra-high-field MRI.Imaging neuroscience (Cambridge, Mass.) · 2025
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Nischal KhanalImaging Science Program, Washington University in St. Louis, St. Louis, Missouri, United States; Mallinckrodt Institute of Radiology, Washington University School of Medicine in St. Louis, 660 S. Euclid Ave, St. Louis, MO 63110, United States. Electronic address: nkhanal@wustl.edu.
Jonah A Padawer-CurryImaging Science Program, Washington University in St. Louis, St. Louis, Missouri, United States; Mallinckrodt Institute of Radiology, Washington University School of Medicine in St. Louis, 660 S. Euclid Ave, St. Louis, MO 63110, United States. Electronic address: j.padawer-curry@wustl.edu.
Trevor VossBiophotonics Center, School of Engineering, Vanderbilt University, Keck FEL Center, Suite 200, 410 24th Ave. South, Nashville, TN 37232, United States. Electronic address: Trevor.r.voss@vanderbilt.edu.
Kevin A SchulteUniversity of Missouri School of Medicine, 1 Hospital Dr, Columbia, MO 65212, United States. Electronic address: kas9tb@health.missouri.edu.
Annie R BiceMallinckrodt Institute of Radiology, Washington University School of Medicine in St. Louis, 660 S. Euclid Ave, St. Louis, MO 63110, United States. Electronic address: abice@wustl.edu.
Adam Q BauerImaging Science Program, Washington University in St. Louis, St. Louis, Missouri, United States; Mallinckrodt Institute of Radiology, Washington University School of Medicine in St. Louis, 660 S. Euclid Ave, St. Louis, MO 63110, United States; Department of Biomedical Engineering, Washington University in St. Louis, St. Louis, Missouri, United States. Electronic address: aqbauer@wustl.edu.

Funding

21ST CENTURY IMAGING SCIENCES: GRADUATE STUDENT TRAININGT32EB014855 · NIBIB · WASHINGTON UNIVERSITY · PI JOSEPH P CULVER, JOSEPH A O'SULLIVAN · 2012 to 2026
$3.1M
Imaging and Reversibility of Cellular and Network Metabolic Dysfunction in Alzheimer's DiseaseRF1AG079503 · NIA · WASHINGTON UNIVERSITY · PI BAUER, ADAM Q, GOYAL, MANU S · 2022 to 2022
$2.2M
OPTOGENETIC MAPPING OF CELL SPECIFIC CONNECTIONS IN THE MOUSE BRAIN AFTER STROKER01NS102870 · NINDS · WASHINGTON UNIVERSITY · PI BAUER, ADAM Q · 2018 to 2022
$2.1M
Determining the efficacy of therapeutic interventions after stroke from cell specific functional connectomesR01NS126326 · NINDS · WASHINGTON UNIVERSITY · PI ADAM Q BAUER · 2023 to 2026
$1.8M
Imaging and Reversibility of Cellular and Network Metabolic Dysfunction in Alzheimer's DiseaseR01AG079503 · NIA · WASHINGTON UNIVERSITY · PI ADAM Q BAUER, Manu S Goyal · 2025 to 2026
$1.4M
Effects of Psychedelics on Brain Function and NeuroplasticityF99NS139512 · NINDS · WASHINGTON UNIVERSITY · PI PADAWER-CURRY, JONAH · 2024 to 2025
$88k
NIA NIH HHS R01 AG079503NIA NIH HHS RF1 AG079503NIBIB NIH HHS T32 EB014855NINDS NIH HHS F99 NS139512NINDS NIH HHS R01 NS102870NINDS NIH HHS R01 NS126326
6 · The paper itself

Abstract

backgroundMotor mapping allows for determining the macroscopic organization of motor circuits and corresponding motor movement representations on the cortex. Techniques such as intracortical microstimulation (ICMS) are robust, but can be time consuming and invasive, making them non-ideal for cortex-wide mapping or longitudinal studies. In contrast, optogenetic motor mapping offers a rapid and minimally invasive technique, enabling mapping with high spatiotemporal resolution. However, motor mapping has seen limited use in tracking 3-dimensonal, multi-limb movements in awake animals. This gap has left open questions regarding the underlying organizational principles of motor control of coordinated, ethologically-relevant movements involving multiple limbs.

objectiveOur first objective was to develop Multi-limb Optogenetic Motor Mapping (MOMM) to concurrently map motor movement representations of multiple limbs with high fidelity in awake mice. Having established MOMM, our next objective was determine whether maps of coordinated and ethologically-relevant motor output were topographically organized on the cortex.

methodsWe combine optogenetic stimulation with a deep learning driven pose-estimation toolbox, DeepLabCut (DLC), and 3-dimensional triangulation to concurrently map motor movements of multiple limbs in awake mice.

resultsMOMM consistently revealed cortical topographies for all mapped features within and across mice. Many motor maps overlapped and were topographically similar. Several motor movement representations extended beyond cytoarchitecturally defined somatomotor cortex. Finer articulations of the forepaw resided within gross motor movement representations of the forelimb. Moreover, many cortical sites exhibited concurrent limb coactivation when photostimulated, prompting the identification of several cortical regions harboring coordinated and ethologically-relevant movements.

conclusionsThe cortex appears to be topographically organized by motor programs, which are responsible for coordinated, multi-limbed, and behavior-like movements.

Indexed as

Brain MappingMotor CortexMovementOptogeneticsAnimalsExtremitiesMaleMiceMice, Inbred C57BLWakefulnessCortical organizationMotor circuitryMotor mappingOptogenetics

Identifiers

PMID39476952
PMCPMC12699988

What Socratic holds

Textmetadata
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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 Socratic graph.