Evidence map›Paper›PMID 31355747›Full record

ArticleeLife2019

Spinal V2b neurons reveal a role for ipsilateral inhibition in speed control.

Rebecca A Callahan, Richard Roberts, Mohini Sengupta, Yukiko Kimura, Shin-Ichi Higashijima, Martha W Bagnall

Open access · goldAbstract read
In one paragraph

Article in eLife, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.3field-weighted citation impact, top 8% of its field
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

30 citing papers in PubMed, 62 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. V2b Neurons Act via Multiple Targets to Produce in Phase Inhibition during Locomotion.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Electrical Synapses Mediate Embryonic Hyperactivity in a Zebrafish Model of Fragile X Syndrome.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
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

6 authors at 2 institutions in 2 countries.

Rebecca A CallahanDepartment of Neuroscience, Washington University School of Medicine, St Louis, United States.
Richard RobertsDepartment of Neuroscience, Washington University School of Medicine, St Louis, United States.
Mohini SenguptaDepartment of Neuroscience, Washington University School of Medicine, St Louis, United States.ORCID 0000-0002-5234-8258
Yukiko KimuraNational Institute for Basic Biology, Okazaki, Japan.ORCID 0000-0001-8381-8622
Shin-Ichi HigashijimaNational Institute for Basic Biology, Okazaki, Japan.ORCID 0000-0001-6350-4992
Martha W BagnallDepartment of Neuroscience, Washington University School of Medicine, St Louis, United States.ORCID 0000-0003-2102-6165
Washington University in St. Louis · USNational Institute for Basic Biology · JP

Funding

SYNAPTIC COMPUTATIONS IN CENTRAL VESTIBULAR NEURONSR01DC016413 · NIDCD · WASHINGTON UNIVERSITY · PI Martha W Bagnall · 2018 to 2026
$2.8M
Vestibular control of axial motor circuitryR00DC012536 · NIDCD · WASHINGTON UNIVERSITY · PI BAGNALL, MARTHA W · 2015 to 2017
$735k
IPSILATERAL INHIBITION IN SPINAL CORD MOTOR CIRCUITSF32NS103247 · NINDS · WASHINGTON UNIVERSITY · PI CALLAHAN, REBECCA ANN · 2017 to 2018
$106k
NIDCD NIH HHS R00 DC012536NIDCD NIH HHS R01 DC016413NINDS NIH HHS F32 NS103247
6 · The paper itself

Abstract

The spinal cord contains a diverse array of interneurons that govern motor output. Traditionally, models of spinal circuits have emphasized the role of inhibition in enforcing reciprocal alternation between left and right sides or flexors and extensors. However, recent work has shown that inhibition also increases coincident with excitation during contraction. Here, using larval zebrafish, we investigate the V2b (Gata3+) class of neurons, which contribute to flexor-extensor alternation but are otherwise poorly understood. Using newly generated transgenic lines we define two stable subclasses with distinct neurotransmitter and morphological properties. These V2b subclasses synapse directly onto motor neurons with differential targeting to speed-specific circuits. In vivo, optogenetic manipulation of V2b activity modulates locomotor frequency: suppressing V2b neurons elicits faster locomotion, whereas activating V2b neurons slows locomotion. We conclude that V2b neurons serve as a brake on axial motor circuits. Together, these results indicate a role for ipsilateral inhibition in speed control.

Indexed as

AnimalsInterneuronsMotionMotor NeuronsMuscle ContractionSpinal CordZebrafishcircuitryinhibitionlocomotionneurosciencespinal cordzebrafish

Identifiers

PMID31355747
PMCPMC6701946
OpenAlexW2966184004

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.