Evidence map›Paper›PMID 29923318›Full record

ArticleDevelopmental neurobiology2018

Intraspinal serotonergic signaling suppresses locomotor activity in larval zebrafish.

Jacob E Montgomery, Sarah Wahlstrom-Helgren, Timothy D Wiggin, Brittany M Corwin, Christina Lillesaar, Mark A Masino

Abstract read
In one paragraph

Article in Developmental neurobiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Serotonergic Control of Spine Morphology During Growth in Zebrafish.bioRxiv : the preprint server for biology · 2026
    Article
  2. Enteroendocrine cells wire the gut-brain vagal axis.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Article
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  6. Review
  7. Article
  8. Article
  9. Article
  10. iScience · 2023
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Serotonin in Animal Cognition and Behavior.International journal of molecular sciences · 2020
    Review
  17. Review
  18. Article
  19. 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

6 authors.

Jacob E MontgomeryDepartment of Neuroscience, University of Minnesota, Minneapolis, Minnesota.ORCID http://orcid.org/0000-0002-0178-982X
Sarah Wahlstrom-HelgrenDepartment of Neuroscience, University of Minnesota, Minneapolis, Minnesota.
Timothy D WigginDepartment of Neuroscience, University of Minnesota, Minneapolis, Minnesota.
Brittany M CorwinDepartment of Neuroscience, University of Minnesota, Minneapolis, Minnesota.
Christina LillesaarDepartment of Physiological Chemistry, University of Würzburg, Biocenter, Würzburg, Germany.
Mark A MasinoDepartment of Neuroscience, University of Minnesota, Minneapolis, Minnesota.

Funding

PREDOCTORAL TRAINING OF NEUROSCIENTISTST32GM008471 · NIGMS · UNIVERSITY OF MINNESOTA TWIN CITIES · PI EBNER, TIMOTHY J · 1993 to 2017
$4.9M
Dopaminergic modulation of spinal locomotor circuitsR01NS094176 · NINDS · UNIVERSITY OF MINNESOTA · PI MASINO, MARK A · 2016 to 2020
$1.7M
Control of Locomotor Activity by Identified Premotor Spinal InterneuronsR01NS065054 · NINDS · UNIVERSITY OF MINNESOTA · PI MASINO, MARK A · 2010 to 2013
$1.3M
V3 Spinal Cord Neurons Participate in Driving Locomotion in VertebratesF31NS083110 · NINDS · UNIVERSITY OF MINNESOTA · PI WIGGIN, TIMOTHY DAVID · 2013 to 2014
$45k
NIGMS NIH HHS T32 GM008471NINDS NIH HHS F31 NS083110NINDS NIH HHS R01 NS065054NINDS NIH HHS R01 NS094176
6 · The paper itself

Abstract

Serotonin (5HT) is a modulator of many vital processes in the spinal cord (SC), such as production of locomotion. In the larval zebrafish, intraspinal serotonergic neurons (ISNs) are a source of spinal 5HT that, despite the availability of numerous genetic and optical tools, has not yet been directly shown to affect the spinal locomotor network. In order to better understand the functions of ISNs, we used a combination of strategies to investigate ISN development, morphology, and function. ISNs were optically isolated from one another by photoconverting Kaede fluorescent protein in individual cells, permitting morphometric analysis as they developed in vivo. ISN neurite lengths and projection distances exhibited the greatest amount of change between 3 and 4 days post-fertilization (dpf) and appeared to stabilize by 5 dpf. Overall ISN innervation patterns were similar between cells and between SC regions. ISNs possessed rostrally-extending neurites resembling dendrites and a caudally-extending neurite resembling an axon, which terminated with an enlarged growth cone-like structure. Interestingly, these enlargements remained even after neurite extension had ceased. Functionally, application of exogenous 5HT reduced spinally-produced motor nerve bursting. A selective 5HT reuptake inhibitor and ISN activation with channelrhodopsin-2 each produced similar effects to 5HT, indicating that spinally-intrinsic 5HT originating from the ISNs has an inhibitory effect on the spinal locomotor network. Taken together this suggests that the ISNs are morphologically mature by 5 dpf and supports their involvement in modulating the activity of the spinal locomotor network. © 2018 Wiley Periodicals, Inc. Develop Neurobiol, 2018.

Indexed as

morphologyoptogeneticserotoninspinal cordzebrafish

Identifiers

PMID29923318
PMCPMC6301152

What OpenQuestion holds

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Registered trials

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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.