Evidence map›Paper›PMID 19587321›Full record

ArticleJournal of neurophysiology2009

Origins of abnormal excitability in biceps brachii motoneurons of spastic-paretic stroke survivors.

Carol J Mottram, Nina L Suresh, C J Heckman, Monica A Gorassini, William Z Rymer

Open access · greenAbstract read
In one paragraph

Article in Journal of neurophysiology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

65 citing papers in PubMed, 129 citations in OpenAlex.

  1. Trial
  2. Trial
  3. The relationship between the flexion synergy and stretch reflexes in individuals with chronic hemiparetic stroke.IEEE ... International Conference on Rehabilitation Robotics : [proceedings] · 2011
    Trial
  4. Review
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  8. Article
  9. Article
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  11. Observational
  12. Article
  13. Article
  14. Article
  15. Article
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  17. Quantifying Altered Neural Connectivity of the Stretch Reflex in Chronic Hemiparetic Stroke.IEEE transactions on neural systems and rehabilitation engineering : a publication of the IEEE Engineering in Medicine and Biology Society · 2020
    Article
  18. Article
  19. Nonlinear Input-Output Functions of Motoneurons.Physiology (Bethesda, Md.) · 2020
    Review
  20. Article

5 more citing papers are in PubMed but not listed here.

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 3 institutions in 2 countries.

Carol J MottramSensory Motor Performance Program, Rehabilitation Institute of Chicago, Chicago, Illinois 60611, USA. c-mottram@northwestern.edu
Nina L Suresh
C J Heckman
Monica A Gorassini
William Z Rymer
Shirley Ryan AbilityLab · USNorthwestern University · USUniversity of Alberta · CA

Funding

ENGINEERING FOR NEUROLOGIC REHABILITATIONR24HD050821 · NICHD · REHABILITATION INSTITUTE OF CHICAGO D/B/A SHIRLEY RYAN ABILITYLAB · PI RYMER, WILLIAM ZEV · 2005 to 2014
$7.9M
PATHOPHYSIOLOGY AND REHABILITATION OF NEURAL DYSFUNCTIONT32HD007418 · NICHD · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Levi John Hargrove · 1992 to 2026
$6.5M
NICHD NIH HHS 2T32 HD-007418-16NICHD NIH HHS 5R24 HD-050821-04
6 · The paper itself

Abstract

Stroke survivors often exhibit abnormal motoneuron excitability, manifested clinically as spasticity with exaggerated stretch reflexes in resting muscles. We examined whether this abnormal excitability is a result of increased activation of intrinsic voltage-dependent persistent inward currents (PICs) or whether it is a result of enhanced synaptic inputs to the motoneuron. This distinction was made by recording firing rate profiles of pairs of motor units during isometric contractions of elbow flexor muscles. To estimate PIC amplitude, the discharge of the lower-threshold (reporter) motor unit of the pair was used to estimate the synaptic input to the higher-threshold (test) motor unit. The estimated synaptic input required to recruit the test unit was compared with the synaptic input when the test unit was derecruited (DeltaF) and this served as an estimate of the intrinsic (PIC) contribution to motoneuron firing. We found that PIC estimates were not larger in spastic-paretic motoneurons (DeltaF = 4.0 +/- 1.6 pps) compared with contralateral (4.6 +/- 1.4 pps) and age-matched healthy control motoneurons (3.8 +/- 1.7, all P > 0.1). Instead, following the voluntary contractions, the majority of lower-threshold motor units in spastic-paretic muscles (83%) exhibited spontaneous discharge, compared with 14% of contralateral and 0% of control motor units. Furthermore, there was strong co-modulation of simultaneously active units in spastic muscle. The presence of ongoing, correlated unit activity at "rest," coupled with firing behavior at recruitment unique to lower-threshold motor units in spastic muscles, suggested that firing changes are likely a result of a low-level depolarizing synaptic drive to the resting motoneuron pool.

Indexed as

Action PotentialsAgedElbowFemaleFunctional LateralityHumansMaleMembrane PotentialsMiddle AgedMotor NeuronsMuscle ContractionMuscle SpasticityParesisStrokeSynapses

Identifiers

PMID19587321
PMCPMC2775372
OpenAlexW2067186423

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.