Evidence map›Paper›PMID 23221401›Full record

ArticleJournal of neurophysiology2013

Reduction of spinal sensory transmission by facilitation of 5-HT1B/D receptors in noninjured and spinal cord-injured humans.

Jessica M D'Amico, Yaqing Li, David J Bennett, Monica A Gorassini

Open access · greenAbstract readControlled Clinical Trial
In one paragraph

Article in Journal of neurophysiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 18% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 49 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. 5-HTThe European journal of neuroscience · 2022
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. 5-HTJournal of neurophysiology · 2019
    Article
  17. Article
  18. Article
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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

4 authors at 1 institution in 1 country.

Jessica M D'AmicoCentre for Neuroscience, Univ. of Alberta, 5-005 Katz Group - Rexall Centre, Edmonton, AB, Canada T6G 2E1.
Yaqing Li
David J Bennett
Monica A Gorassini
University of Alberta · CA

Funding

Motoneuron Properties in Chronic Spinal InjuryR01NS047567 · NINDS · UNIVERSITY OF ALBERTA · PI BENNETT, DAVID JAMES, FOUAD, KARIM · 2004 to 2020
$4.0M
Canadian Institutes of Health Research MOP-106549Canadian Institutes of Health Research MOP-14697NINDS NIH HHS R01 NS047567
6 · The paper itself

Abstract

Activation of receptors by serotonin (5-HT1) and norepinephrine (α2) on primary afferent terminals and excitatory interneurons reduces transmission in spinal sensory pathways. Loss or reduction of descending sources of serotonin and norepinephrine after spinal cord injury (SCI) and the subsequent reduction of 5-HT1/α2 receptor activity contributes, in part, to the emergence of excessive motoneuron activation from sensory afferent pathways and the uncontrolled triggering of persistent inward currents that depolarize motoneurons during muscle spasms. We tested in a double-blind, placebo-controlled study whether facilitating 5-HT1B/D receptors with the agonist zolmitriptan reduces the sensory activation of motoneurons during an H-reflex in both noninjured control and spinal cord-injured participants. In both groups zolmitriptan, but not placebo, reduced the size of the maximum soleus H-reflex with a peak decrease to 59% (noninjured) and 62% (SCI) of predrug values. In SCI participants we also examined the effects of zolmitriptan on the cutaneomuscular reflex evoked in tibialis anterior from stimulation to the medial arch of the foot. Zolmitriptan, but not placebo, reduced the long-latency, polysynaptic component of the cutaneomuscular reflex (first 200 ms of reflex) by ∼50%. This ultimately reduced the triggering of the long-lasting component of the reflex (500 ms poststimulation to end of reflex) known to be mediated by persistent inward currents in the motoneuron. These results demonstrate that facilitation of 5-HT1B/D receptors reduces sensory transmission in both monosynaptic and polysynaptic reflex pathways to ultimately reduce long-lasting reflexes (spasms) after SCI.

Indexed as

Action PotentialsAdultDouble-Blind MethodFemaleH-ReflexHumansMaleMiddle AgedMotor NeuronsMuscle, SkeletalMuscle SpasticityOxazolidinonesReceptors, Adrenergic, alpha-2Receptor, Serotonin, 5-HT1BReceptor, Serotonin, 5-HT1DSerotonin 5-HT1 Receptor AgonistsOxazolidinonesReceptors, Adrenergic, alpha-2Receptor, Serotonin, 5-HT1BReceptor, Serotonin, 5-HT1DSerotonin 5-HT1 Receptor AgonistsTryptamineszolmitriptan

Identifiers

PMID23221401
PMCPMC3602943
OpenAlexW2088090269

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.