Evidence map›Paper›PMID 20107061›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2010

Readiness discharge for spontaneous initiation of walking in crayfish.

Katsushi Kagaya, Masakazu Takahata

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

15 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. What Is the Readiness Potential?Trends in cognitive sciences · 2021
    Review
  6. Article
  7. Reckoning the moment of reckoning in spontaneous voluntary movement.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  8. Article
  9. Free will and paranormal beliefs.Frontiers in psychology · 2014
    Article
  10. Designing and implementing nervous system simulations on LEGO robots.Journal of visualized experiments : JoVE · 2013
    Article
  11. Article
  12. Article
  13. An accumulator model for spontaneous neural activity prior to self-initiated movement.Proceedings of the National Academy of Sciences of the United States of America · 2012
    Article
  14. Specialized brain regions and sensory inputs that control locomotion in leeches.Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology · 2012
    Article
  15. 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

2 authors at 2 institutions in 1 country.

Katsushi KagayaDivision of Biological Sciences, Graduate School of Science, Department of Life Sciences, Faculty of Science, Hokkaido University, Sapporo 060-0810, Japan. kagaya@sci.hokudai.ac.jp
Masakazu Takahata
Hokkaido University · JPHokkaido University of Science · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Animals initiate behavior not only reflexively but also spontaneously in the absence of external stimuli. In vertebrates, electrophysiological data on the neuronal activity associated with the self-initiated voluntary behavior have accumulated extensively. In invertebrates, however, little is known about the neuronal basis of the spontaneous initiation of behavior. We investigated the spike activity of brain neurons at the time of spontaneous initiation of walking in the crayfish Procambarus clarkii and found neuronal signals indicative of readiness or preparatory activities in the vertebrate brain that precede the onset of voluntary actions. Those readiness discharge neurons became active >1 s before the initiation of walking regardless of stepping direction. They remained inactive at the onset of mechanical stimulus-evoked walking in which other descending units were recruited. These results suggest that the parallel descending mechanisms from the brain separately subserve the spontaneous and stimulus-evoked walking. Electrical stimulation of these different classes of neurons caused different types of walking. In addition, we found other descending units that represented different aspects of walking, including those units that showed a sustained activity increase throughout the walking bout depending on its stepping direction, as well as one veto unit for canceling out the output effect of the readiness discharge and three termination units for stopping the walking behavior. These findings suggest that the descending activities are modularized in parallel for spontaneous initiation, continuation, and termination of walking, constituting a sequentially hierarchical control.

Indexed as

Action PotentialsAnimalsAstacoideaAxonsBrainEfferent PathwaysElectric StimulationElectrophysiologyExtremitiesFemaleFunctional LateralityGanglia, InvertebrateLocomotionMaleModels, AnimalMotor Neurons

Identifiers

PMID20107061
PMCPMC6633775
OpenAlexW2076096786

What OpenQuestion holds

Textmetadata
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.