Evidence map›Paper›PMID 22580045›Full record

ArticleBiochemical pharmacology2012

The nicotinic acetylcholine receptors of zebrafish and an evaluation of pharmacological tools used for their study.

Roger L Papke, Fumihito Ono, Clare Stokes, Jason M Urban, R Thomas Boyd

Open access · greenAbstract read
In one paragraph

Article in Biochemical pharmacology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

27 citing papers in PubMed, 57 citations in OpenAlex.

  1. Nicotine and Cytisine Embryotoxicity in the Experimental Zebrafish Model.International journal of molecular sciences · 2023
    Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
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  10. Article
  11. Article
  12. Article
  13. Identification ofeLife · 2020
    Article
  14. Assessing the hazard of E-Cigarette flavor mixtures using zebrafish.Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association · 2020
    Article
  15. Article
  16. Article
  17. Review
  18. Zebrafish mutants of the neuromuscular junction: swimming in the gene pool.The journal of physiological sciences : JPS · 2015
    Review
  19. Article
  20. Molecular psychiatry of zebrafish.Molecular psychiatry · 2015
    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

5 authors at 3 institutions in 1 country.

Roger L PapkeDepartment of Pharmacology, University of Florida College of Medicine, Gainesville, FL, USA. rlpapke@ufl.edu
Fumihito Ono
Clare Stokes
Jason M Urban
R Thomas Boyd
Florida College · USNational Institute on Alcohol Abuse and Alcoholism · USThe Ohio State University · US

Funding

UF Clinical and Translational Science AwardUL1TR000064 · NCATS · UNIVERSITY OF FLORIDA · PI NELSON, DAVID R · 2012 to 2014
$12.2M
Targeting of Alpha7 nAChR for therapeutic effectsR01GM057481 · NIGMS · UNIVERSITY OF FLORIDA · PI PAPKE, ROGER L · 2000 to 2023
$7.6M
In vivo studies of neural system in zebrafishZIAAA000437 · NIAAA · NATIONAL INSTITUTE ON ALCOHOL ABUSE AND ALCOHOLISM · PI ONO, FUMIHITO · 2009 to 2015
$5.2M
Intramural NIH HHSNCATS NIH HHS UL1 TR000064NIGMS NIH HHS GM57481NIGMS NIH HHS R01 GM057481
6 · The paper itself

Abstract

Zebrafish (Danio rerio) have been used to study multiple effects of nicotine, for example on cognition, locomotion, and stress responses, relying on the assumption that pharmacological tools will operate similarly upon molecular substrates in the fish and mammalian systems. We have cloned the zebrafish nicotinic acetylcholine receptor (nAChR) subunits and expressed key nAChR subtypes in Xenopus oocytes including neuronal (α4β2, α2β2, α3β4, and α7) and muscle (α1β1(b)ɛδ) nAChR. Consistent with studies of mammalian nAChR, nicotine was relatively inactive on muscle-type receptors, having both low potency and efficacy. It had high efficacy but low potency for α7 receptors, and the best potency and good efficacy for α4β2 receptors. Cytisine, a key lead compound for the development of smoking cessation agents, is a full agonist for both mammalian α7 and α3β4 receptors, but a full agonist only for the fish α7, with surprisingly low efficacy for α3β4. The efficacy of cytisine for α4β2 was somewhat greater than typically reported for mammalian α4β2. The ganglionic blocker mecamylamine was most potent for blocking α3β4 receptors, least potent for α7, and roughly equipotent for the muscle receptors and the β2-containing nAChR. However, the block of β2-containing receptors was slowly reversible, consistent with effective targeting of these CNS-type receptors in vivo. Three prototypical α7-selective agonists, choline, tropane, and 4OH-GTS-21, were tested, and these agents were observed to activate both fish α7 and α4β2 nAChR. Our data therefore indicate that while some pharmacological tools used in zebrafish may function as expected, others will not.

Indexed as

Amino Acid SequenceAnimalsCattleChick EmbryoDose-Response Relationship, DrugDrug Evaluation, PreclinicalHumansMiceMolecular Sequence DataNicotinic AgonistsNicotinic AntagonistsRatsReceptors, NicotinicSpecies SpecificityXenopus laevisZebrafishNicotinic AgonistsNicotinic AntagonistsReceptors, Nicotinic

Identifiers

PMID22580045
PMCPMC3372685
OpenAlexW2158199896

What OpenQuestion holds

Textmetadata
LicenceTDM
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.