Evidence map›Paper›PMID 23015438›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2012

The conserved dopaminergic diencephalospinal tract mediates vertebrate locomotor development in zebrafish larvae.

Aaron M Lambert, Joshua L Bonkowsky, Mark A Masino

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers.

0numbers the graph read from it
0cells of the map it votes in
79citing 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

79 citing papers in PubMed.

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  16. In Vivo Evaluation ofPharmaceuticals (Basel, Switzerland) · 2021
    Article
  17. Article
  18. Article
  19. Variants inHGG advances · 2021
    Article
  20. Article

19 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

3 authors.

Aaron M LambertDepartment of Neuroscience, University of Minnesota, Minneapolis, Minnesota 55455, USA.
Joshua L Bonkowsky
Mark A Masino

Funding

Trans-Cellular Activation of Transcription to Analyze Dopaminergic Axon ReorganizDP2MH100008 · NIMH · UNIVERSITY OF UTAH · PI BONKOWSKY, JOSH LEITCH · 2012 to 2012
$2.2M
Translational Research in Neurobiolgy of Disease Training ProgramT32DA022616 · NIDA · UNIVERSITY OF MINNESOTA · PI LOW, WALTER C · 2006 to 2010
$1.4M
Control of Locomotor Activity by Identified Premotor Spinal InterneuronsR01NS065054 · NINDS · UNIVERSITY OF MINNESOTA · PI MASINO, MARK A · 2010 to 2013
$1.3M
Characterization and Genetic Analysis of Basal Ganglia Axon PathfindingK08DA024753 · NIDA · UNIVERSITY OF UTAH · PI BONKOWSKY, JOSH LEITCH · 2008 to 2013
$931k
NIDA NIH HHS K08 DA024753NIDA NIH HHS T32 DA022616NIDA NIH HHS T32-DA022616NIMH NIH HHS DP2 MH100008NINDS NIH HHS R01 NS065054NINDS NIH HHS R01-NS065054
6 · The paper itself

Abstract

The most conserved part of the vertebrate dopaminergic system is the orthopedia (otp)-expressing diencephalic neuronal population that constitutes the dopaminergic diencephalospinal tract (DDT). Although studies in the neonatal murine spinal cord in vitro suggest an early locomotor role of the DDT, the function of the DDT in developing vertebrates in vivo remains unknown. Here, we investigated the role of the DDT in the locomotor development of zebrafish larvae. To assess the development of the behavioral and neural locomotor pattern, we used high-throughput video tracking in combination with peripheral nerve recordings. We found a behavioral and neural correspondence in the developmental switch from an immature to mature locomotor pattern. Blocking endogenous dopamine receptor 4 (D(4)R) signaling in vivo either before or after the developmental switch prevented or reversed the switch, respectively. Spinal transections of post-switch larvae reestablished the immature locomotor pattern, which was rescued to a mature-like pattern via spinal D(4)R agonism. Selective chemogenetic ablation of otp b (otpb) neurons that contribute to the DDT perpetuated the immature locomotor pattern in vivo. This phenotype was recapitulated by diencephalic transections that removed the dopaminergic otpb population and was rescued to a mature-like locomotor pattern by D(4)R agonism. We conclude that the dopaminergic otpb population, via the DDT, is responsible for spinal D(4)R signaling to mediate the developmental switch to the mature locomotor pattern of zebrafish. These results, integrated with the mammalian literature, suggest that the DDT represents an evolutionarily conserved neuromodulatory system that is necessary for normal vertebrate locomotor development.

Indexed as

Analysis of VarianceAnimalsAnimals, Genetically ModifiedDiencephalonDopamineDopamine AgentsDose-Response Relationship, DrugElectrophysiologyExcitatory Amino Acid AgonistsGreen Fluorescent ProteinsIn Situ Nick-End LabelingLarvaLocomotionMetronidazoleNeural PathwaysNeuronsDopamineDopamine Agentsenhanced green fluorescent proteinExcitatory Amino Acid AgonistsGreen Fluorescent ProteinsMetronidazoleNitroreductasesN-Methylaspartateorthopedia protein, zebrafishReceptors, Dopamine D4Transcription FactorsZebrafish Proteins

Identifiers

PMID23015438
PMCPMC3481997

What OpenQuestion holds

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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.