Evidence map›Paper›PMID 20506479›Full record

ArticleThe Journal of comparative neurology2010

Regenerated synapses in lamprey spinal cord are sparse and small even after functional recovery from injury.

Paul A Oliphint, Naila Alieva, Andrea E Foldes, Eric D Tytell, Billy Y-B Lau, Jenna S Pariseau, Avis H Cohen, Jennifer R Morgan

Abstract read
In one paragraph

Article in The Journal of comparative neurology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
–field-weighted citation impact
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

33 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Proprioceptive feedback amplification restores effective locomotion in a neuromechanical model of lampreys with spinal injuries.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  6. Article
  7. Article
  8. Article
  9. Semaphorin signaling restricts neuronal regeneration inFrontiers in cell and developmental biology · 2022
    Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  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

8 authors.

Paul A OliphintSection of Molecular Cell and Developmental Biology; Institute for Cell and Molecular Biology, Institute for Neuroscience, University of Texas at Austin, Austin, Texas 78712, USA.
Naila Alieva
Andrea E Foldes
Eric D Tytell
Billy Y-B Lau
Jenna S Pariseau
Avis H Cohen
Jennifer R Morgan

Funding

CRCNS: An Integrated Locomotion Model for Lamprey SwimmingR01NS054271 · NINDS · UNIV OF MARYLAND, COLLEGE PARK · PI COHEN, AVIS H · 2005 to 2009
$1.5M
NINDS NIH HHS R01 NS054271NINDS NIH HHS R01NS05427102
6 · The paper itself

Abstract

Despite the potential importance that synapse regeneration plays in restoring neuronal function after spinal cord injury (SCI), even the most basic questions about the morphology of regenerated synapses remain unanswered. Therefore, we set out to gain a better understanding of central synapse regeneration by examining the number, distribution, molecular composition, and ultrastructure of regenerated synapses under conditions in which behavioral recovery from SCI was robust. To do so, we used the giant reticulospinal (RS) neurons of lamprey spinal cord because they readily regenerate, are easily identifiable, and contain large synapses that serve as a classic model for vertebrate excitatory neurotransmission. Using a combination of light and electron microscopy, we found that regenerated giant RS synapses regained the basic structures and presynaptic organization observed at control giant RS synapses at a time when behavioral recovery was nearly complete. However, several obvious differences remained. Most strikingly, regenerated giant RS axons produced very few synapses. In addition, presynaptic sites within regenerated axons were less complex, had fewer vesicles, and had smaller active zones than normal. In contrast, the densities of presynapses and docked vesicles were nearly restored to control values. Thus, robust functional recovery from SCI can occur even when the structures of regenerated synapses are sparse and small, suggesting that functional recovery is due to a more complex set of compensatory changes throughout the spinal network.

Indexed as

Nerve RegenerationRecovery of FunctionAnimalsAxonsBiomechanical PhenomenaGap JunctionsLarvaNeuronsPetromyzonPresynaptic TerminalsSpinal Cord InjuriesSwimmingSynapsesSynaptic VesiclesTime Factors

Identifiers

PMID20506479
PMCPMC4533873

What OpenQuestion holds

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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.