Evidence map›Paper›PMID 28381489›Full record

ArticleJournal of neurophysiology2017

Parallel processing of internal and external feedback in the spinocerebellar system of primates.

Oren Cohen, Ran Harel, Tim D Aumann, Zvi Israel, Yifat Prut

Abstract read
In one paragraph

Article in Journal of neurophysiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

6 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Sensorimotor anatomy of gait, balance, and falls.Handbook of clinical neurology · 2018
    Review
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

5 authors at 4 institutions in 2 countries.

Oren CohenDepartment of Medical Neurobiology, Institute for Medical Research Israel-Canada and The Edmond & Lily Safra Center for Brain Sciences, The Hebrew University of Jerusalem, Hadassah Medical School, Jerusalem, Israel.
Ran HarelDepartment of Neurosurgery, Sheba Medical Center, Tel Aviv, Israel.
Tim D AumannFlorey Institute of Neuroscience and Mental Health, The University of Melbourne, Melbourne, Australia; and.
Zvi IsraelDepartment of Neurosurgery, Hadassah Hospital, Jerusalem, Israel.
Yifat PrutDepartment of Medical Neurobiology, Institute for Medical Research Israel-Canada and The Edmond & Lily Safra Center for Brain Sciences, The Hebrew University of Jerusalem, Hadassah Medical School, Jerusalem, Israel; yifatpr@ekmd.huji.ac.il.
Hebrew University of Jerusalem · ILHerzog Hospital · ILSheba Medical Center · ILUniversity of Melbourne · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cerebellar control of voluntary movements is achieved by the integration of external and internal feedback information to adjust and correct properly ongoing actions. In the forelimb of primates, rostral-spinocerebellar tract (RSCT) neurons are thought to integrate segmental, descending, and afferent sources and relay upstream a compound signal that contains both an efference copy of the spinal-level motor command and the state of the periphery. We tested this hypothesis by implanting stimulating electrodes in the superior cerebellar peduncle and recording the activity of cervical spinal neurons in primates. To dissociate motor commands and proprioceptive signals, we used a voluntary wrist task and applied external perturbations to the movement. We identified a large group of antidromically activated RSCT neurons located in deep dorsal sites and a smaller fraction of postsynaptically activated (PSA) cells located in intermediate and ventral laminae. RSCT cells received sensory input from broad, proximally biased receptive fields (RFs) and were not affected by applied wrist perturbations. PSA cells received sensory information from distal RFs and were more strongly related to active and passive movements. The anatomical and functional properties of RSCT and PSA cells suggest that descending signals converging on PSA cells contribute to both motor preparation and motor control. In parallel, RSCT neurons relay upstream an integrated signal that encodes the state of working muscles and can contribute to distal-to-proximal coordination of action. Thus the rostral spinocerebellar system sends upstream an efference copy of the motor command but does not signal abrupt errors in the performed movement.

Indexed as

Feedback, PhysiologicalProprioceptionAnimalsEvoked Potentials, MotorMacaca fascicularisNeuronsSpinocerebellar Tractsmotor controlprimatesspinocerebellarvoluntary movements

Identifiers

PMID28381489
PMCPMC5498734
OpenAlexW2604660342

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.