Evidence map›Paper›PMID 15331683›Full record

ArticleThe Journal of physiology2004

Neuroepithelial oxygen chemoreceptors of the zebrafish gill.

Michael G Jonz, Ian M Fearon, Colin A Nurse

Open access · greenAbstract readComparative Study
In one paragraph

Article in The Journal of physiology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

41 citing papers in PubMed, 216 citations in OpenAlex.

  1. Article
  2. Specialized gas-exchange endothelium of the zebrafish gill.bioRxiv : the preprint server for biology · 2025
    Article
  3. Article
  4. Article
  5. Oxygen chemoreceptor inhibition by dopamine DThe Journal of physiology · 2025
    Article
  6. Structure and function of the larval teleost fish gill.Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology · 2024
    Review
  7. Gulf toadfish (Opsanus beta) gill neuroepithelial cells in response to hypoxia exposure.Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology · 2024
    Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. Review
  15. The development of the OJournal of comparative physiology. B, Biochemical, systemic, and environmental physiology · 2021
    Article
  16. Review
  17. Does blood flow limit acute hypoxia performance in larval zebrafish (Danio rerio)?Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology · 2021
    Article
  18. Hydrogen sulphide sensitivity and tolerance in genetically distinct lineages of a selfing mangrove fish (Kryptolebias marmoratus).Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology · 2020
    Article
  19. The role of TASK-2 channels in COAmerican journal of physiology. Regulatory, integrative and comparative physiology · 2020
    Article
  20. Hypoxia attenuate ionic transport in the isolated gill epithelium of Carcinus maenas.Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology · 2020
    Article
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 at 1 institution in 1 country.

Michael G JonzDepartment of Biology, McMaster University, 1280 Main Street West, Hamilton, ON, Canada L8S 4K1.
Ian M Fearon
Colin A Nurse
McMaster University · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In aquatic vertebrates, hypoxia induces physiological changes that arise principally from O(2) chemoreceptors of the gill. Neuroepithelial cells (NECs) of the zebrafish gill are morphologically similar to mammalian O(2) chemoreceptors (e.g. carotid body), suggesting that they may play a role in initiating the hypoxia response in fish. We describe morphological changes of zebrafish gill NECs following in vivo exposure to chronic hypoxia, and characterize the cellular mechanisms of O(2) sensing in isolated NECs using patch-clamp electrophysiology. Confocal immunofluorescence studies indicated that chronic hypoxia (P(O(2)) = 35 mmHg, 60 days) induced hypertrophy, proliferation and process extension in NECs immunoreactive for serotonin or synaptic vesicle protein (SV2). Under voltage clamp, NECs responded to hypoxia (P(O(2)) = 25-140 mmHg) with a dose-dependent decrease in K(+) current. The current-voltage relationship of the O(2)-sensitive current (I(KO(2))) reversed near E(K) and displayed open rectification. Pharmacological characterization indicated that I(KO(2)) was resistant to 20 mM tetraethylammonium (TEA) and 5 mM 4-aminopyridine (4-AP), but was sensitive to 1 mm quinidine. In current-clamp recordings, hypoxia produced membrane depolarization associated with a conductance decrease; this depolarization was blocked by quinidine, but was insensitive to TEA and 4-AP. These biophysical and pharmacological characteristics suggest that hypoxia sensing in zebrafish gill NECs is mediated by inhibition of a background K(+) conductance, which generates a receptor potential necessary for neurosecretion and activation of sensory pathways in the gill. This appears to be a fundamental mechanism of O(2) sensing that arose early in vertebrate evolution, and was adopted later in mammalian O(2) chemoreceptors.

Indexed as

AnimalsChemoreceptor CellsGillsHypoxia, BrainIn Vitro TechniquesMembrane PotentialsNeuroepithelial CellsOxygenQuinidineZebrafishOxygenQuinidine

Identifiers

PMID15331683
PMCPMC1665292
OpenAlexW2133814656

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.