Evidence map›Paper›PMID 40531617›Full record

ArticleCell reports2025

The spinal premotor network driving scratching flexor and extensor alternation.

Mingchen Yao, Akira Nagamori, Sandrina Campos Maçãs, Eiman Azim, Tatyana Sharpee, Martyn Goulding, David Golomb, Graziana Gatto

Abstract read
In one paragraph

Article in Cell reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Mingchen YaoComputational Neurobiology Laboratory, Salk Institute for Biological Studies, La Jolla, CA, USA; Department of Physics, UCSD, La Jolla, CA, USA.
Akira NagamoriMolecular Neurobiology Laboratory, Salk Institute for Biological Studies, La Jolla, CA, USA.
Sandrina Campos MaçãsClinic and Policlinic for Neurology, University Hospital Cologne, Cologne, Germany.
Eiman AzimMolecular Neurobiology Laboratory, Salk Institute for Biological Studies, La Jolla, CA, USA. Electronic address: eazim@salk.edu.
Tatyana SharpeeComputational Neurobiology Laboratory, Salk Institute for Biological Studies, La Jolla, CA, USA; Department of Physics, UCSD, La Jolla, CA, USA. Electronic address: sharpee@salk.edu.
Martyn GouldingMolecular Neurobiology Laboratory, Salk Institute for Biological Studies, La Jolla, CA, USA. Electronic address: goulding@salk.edu.
David GolombDepartments of Physiology and Cell Biology and Physics, Ben Gurion University, Be'er-Sheva 8410501, Israel; School of Brain Sciences and Cognition, Ben Gurion University, Be'er-Sheva 8410501, Israel. Electronic address: golomb@bgu.ac.il.
Graziana GattoClinic and Policlinic for Neurology, University Hospital Cologne, Cologne, Germany. Electronic address: graziana.gatto@uk-koeln.de.

Funding

Spinal Circuits for the Control of Dextrous MovementU19NS112959 · NINDS · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI AZIM, EIMAN · 2019 to 2023
$14.3M
Spinal circuits for mechanical itch and light touchR35NS111643 · NINDS · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI Martyn D Goulding · 2019 to 2026
$9.7M
Functional dissection of cerebellar output circuits that orchestrate limb motor controlRF1NS128898 · NINDS · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI AZIM, EIMAN, CHEN, ALBERT · 2022 to 2022
$2.3M
Functional dissection of cerebellar output circuits that orchestrate limb motor controlR01NS128898 · NINDS · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI EIMAN AZIM, Albert Chen · 2025 to 2026
$1.3M
Defining the contributions of proprioception to goal-directed reaching movementsF32NS126231 · NINDS · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI NAGAMORI, AKIRA · 2022 to 2024
$177k
NINDS NIH HHS F32 NS126231NINDS NIH HHS R01 NS128898NINDS NIH HHS R35 NS111643NINDS NIH HHS RF1 NS128898NINDS NIH HHS U19 NS112959
6 · The paper itself

Abstract

Rhythmic motor behaviors are generated by neural networks termed central pattern generators (CPGs). Although locomotor CPGs have been extensively characterized, it remains unknown how the neuronal populations composing them interact to generate adaptive rhythms in mammals. We explored the cooperation dynamics among the three main populations of ipsilaterally projecting spinal CPG neurons-V1, V2a, and V2b neurons-in scratch reflex rhythmogenesis. Individual ablation of the three neuronal populations reduced the oscillation frequency. Activation of excitatory V2a neurons enhanced the oscillation frequency, while activating inhibitory V1 neurons suppressed movement. Building on these findings, we developed a neuromechanical model made of self-oscillating flexor and extensor modules coupled via inhibition. Rhythm frequency is increased by strong intra-module inhibition and facilitation mechanisms in excitatory neurons and decreased by strong inter-module inhibition. In sum, we describe how genetically identified neuron types and the strengths of their synaptic connections drive scratch rhythmogenesis.

Indexed as

Central Pattern GeneratorsNerve NetSpinal CordAnimalsLocomotionMiceMotor NeuronsNeuronsCPGsCP: Neuroscienceinhibitionmodelingneuronal perturbationsreflexesrhythmogenesissensorimotor responsesspinal cord circuits

Identifiers

PMID40531617
PMCPMC12277023

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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.