Evidence map›Paper›PMID 30588759›Full record

ArticleGenes, brain, and behavior2019

Novel zebrafish behavioral assay to identify modifiers of the rapid, nongenomic stress response.

Han B Lee, Tanya L Schwab, Ashley N Sigafoos, Jennifer L Gauerke, Randall G Krug, MaKayla R Serres, Dakota C Jacobs, Ryan P Cotter, Biswadeep Das, Morgan O Petersen and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Genes, brain, and behavior, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 10% 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

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 67 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Exploring the Toxicity and Therapeutic Potential ofInternational journal of molecular sciences · 2025
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Multiple faces of stress in the zebrafish (Frontiers in physiology · 2024
    Article
  18. iScience · 2023
    Article
  19. Review
  20. Review
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

14 authors at 1 institution in 1 country.

Han B LeeNeuroscience Graduate Program, Mayo Clinic Graduate School of Biomedical Sciences, Rochester, Minnesota.ORCID 0000-0002-6633-966X
Tanya L SchwabDepartment of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, Minnesota.
Ashley N SigafoosDepartment of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, Minnesota.
Jennifer L GauerkeDepartment of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, Minnesota.
Randall G KrugNeuroscience Graduate Program, Mayo Clinic Graduate School of Biomedical Sciences, Rochester, Minnesota.
MaKayla R SerresDepartment of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, Minnesota.
Dakota C JacobsDepartment of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, Minnesota.
Ryan P CotterDepartment of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, Minnesota.
Biswadeep DasDepartment of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, Minnesota.
Morgan O PetersenDepartment of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, Minnesota.
Camden L DabyDepartment of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, Minnesota.
Rhianna M UrbanDepartment of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, Minnesota.
Bethany C BerryDepartment of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, Minnesota.
Karl J ClarkNeuroscience Graduate Program, Mayo Clinic Graduate School of Biomedical Sciences, Rochester, Minnesota.ORCID 0000-0002-9637-0967
Mayo Clinic · US

Funding

PILOT AND FEASIBILTY PROGRAMP30DK084567 · NIDDK · MAYO CLINIC ROCHESTER · PI Samar Ibrahim · 2009 to 2026
$22.2M
Systematic Vertebrate Functional GenomicsR01GM063904 · NIGMS · UNIVERSITY OF TEXAS AT AUSTIN · PI EKKER, STEPHEN CARL · 2001 to 2025
$10.7M
Systematic Vertebrate Functional GenomicsR56GM063904 · NIGMS · MAYO CLINIC ROCHESTER · PI EKKER, STEPHEN CARL · 2009 to 2010
$611k
Developing zebrafish models to reveal interactions between stress and addictionR21DA032194 · NIDA · MAYO CLINIC ROCHESTER · PI CLARK, KARL J · 2011 to 2012
$394k
NIDA NIH HHS DA032194NIDA NIH HHS R21 DA032194NIDDK NIH HHS DK84567NIDDK NIH HHS P30 DK084567NIGMS NIH HHS GM63904NIGMS NIH HHS R01 GM063904NIGMS NIH HHS R56 GM063904
6 · The paper itself

Abstract

When vertebrates face acute stressors, their bodies rapidly undergo a repertoire of physiological and behavioral adaptations, which is termed the stress response. Rapid changes in heart rate and blood glucose levels occur via the interaction of glucocorticoids and their cognate receptors following hypothalamic-pituitary-adrenal axis activation. These physiological changes are observed within minutes of encountering a stressor and the rapid time domain rules out genomic responses that require gene expression changes. Although behavioral changes corresponding to physiological changes are commonly observed, it is not clearly understood to what extent hypothalamic-pituitary-adrenal axis activation dictates adaptive behavior. We hypothesized that rapid locomotor response to acute stressors in zebrafish requires hypothalamic-pituitary-interrenal (HPI) axis activation. In teleost fish, interrenal cells are functionally homologous to the adrenocortical layer. We derived eight frameshift mutants in genes involved in HPI axis function: two mutants in exon 2 of mc2r (adrenocorticotropic hormone receptor), five in exon 2 or 5 of nr3c1 (glucocorticoid receptor [GR]) and two in exon 2 of nr3c2 (mineralocorticoid receptor [MR]). Exposing larval zebrafish to mild environmental stressors, acute changes in salinity or light illumination, results in a rapid locomotor response. We show that this locomotor response requires a functioning HPI axis via the action of mc2r and the canonical GR encoded by nr3c1 gene, but not MR (nr3c2). Our rapid behavioral assay paradigm based on HPI axis biology can be used to screen for genetic and environmental modifiers of the hypothalamic-pituitary-adrenal axis and to investigate the effects of corticosteroids and their cognate receptor interactions on behavior.

Indexed as

Behavior, AnimalLocomotionStress, PhysiologicalAnimalsHypothalamo-Hypophyseal SystemMutationPituitary-Adrenal SystemReceptors, CorticotropinReceptors, GlucocorticoidReceptors, MineralocorticoidZebrafishZebrafish ProteinsReceptors, CorticotropinReceptors, GlucocorticoidReceptors, MineralocorticoidZebrafish Proteinsassay developmentbehavioral geneticscortisolcustom nucleaseglucocorticoid receptorHPA axis

Identifiers

PMID30588759
PMCPMC6446827
OpenAlexW2908501762

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.