Evidence map›Paper›PMID 24081450›Full record

ArticlePflugers Archiv : European journal of physiology2014

THIK-1 (K2P13.1) is a small-conductance background K(+) channel in rat trigeminal ganglion neurons.

Dawon Kang, James O Hogan, Donghee Kim

Abstract read
In one paragraph

Article in Pflugers Archiv : European journal of physiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

22 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
  2. Structure of the human KNature structural & molecular biology · 2025
    Article
  3. Gating mechanism of the two-pore-domain potassium channel THIK1.Nature structural & molecular biology · 2025
    Article
  4. Cryo-EM structure of the human THIK-1 K2P KNature structural & molecular biology · 2025
    Article
  5. The cryo-EM structure and physical basis for anesthetic inhibition of the THIK1 K2P channel.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  6. Structure of the human KbioRxiv : the preprint server for biology · 2024
    Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Higher expression of KCNK10 (TREK-2) KPflugers Archiv : European journal of physiology · 2021
    Article
  13. Verapamil Inhibits TRESK (KInternational journal of molecular sciences · 2018
    Article
  14. Adenosine AThe Journal of physiology · 2018
    Article
  15. Genes linked to species diversity in a sexually dimorphic communication signal in electric fish.Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology · 2018
    Article
  16. Role of K₂p channels in stimulus-secretion coupling.Pflugers Archiv : European journal of physiology · 2015
    Review
  17. Review
  18. Article
  19. Article
  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

3 authors at 2 institutions in 2 countries.

Dawon KangDepartment of Physiology and Biophysics, Chicago Medical School, Rosalind Franklin University of Medicine and Science, 3333 Green Bay Road, North Chicago, IL, 60064, USA.
James O Hogan
Donghee Kim
Rosalind Franklin University of Medicine and Science · USGyeongsang National University · KR

Funding

Mechanism of oxygen sensing by chemoreceptor cellsR01HL111497 · NHLBI · ROSALIND FRANKLIN UNIV OF MEDICINE & SCI · PI KIM, DONGHEE · 2012 to 2015
$1.4M
NHLBI NIH HHS R01 HL111497
6 · The paper itself

Abstract

The goal of this study was to determine the molecular identity of a small-conductance (~5-pS) background K(+) channel expressed in trigeminal ganglion (TG) neurons. We tested the hypothesis that the 5-pS channel is a K2P channel by comparing the pharmacological and single-channel properties of THIK-1 expressed in HEK293 cells. As reported earlier, whole-cell THIK-1 current was inhibited by halothane and activated by arachidonic acid. Among 25 additional modulators tested, bupivacaine (100 μM), quinidine (50 μM) and Ba(2+) (3 mM) and cold (10 °C) were most effective inhibitors of THIK-1 current (>50 % inhibition). In cell-attached patches with high KCl in the pipette and bath solutions, THIK-1 produced a small-conductance (~5 pS) channel with a weak inwardly rectifying current-voltage relationship. Halothane, bupivacaine and cold inhibited the single-channel activities of both THIK-1 and the 5-pS channel in TG neurons, whereas arachidonic acid augmented them. THIK-1 expressed in HEK293 cells and the 5-pS channels in TG neurons were insensitive to hypoxia. Reverse transcriptase-PCR, Western blot and immunocytochemical analyses suggested that THIK-1 mRNA and protein were expressed in TG neurons. These results show that THIK-1 is functionally expressed in TG neurons and contributes to the background K(+) conductance.

Indexed as

Action PotentialsAnimalsCell HypoxiaCells, CulturedHEK293 CellsHumansNeuronsPotassium Channel BlockersPotassium Channels, Tandem Pore DomainRatsRNA, MessengerTrigeminal GanglionKcnk13 protein, ratPotassium Channel BlockersPotassium Channels, Tandem Pore DomainRNA, Messenger

Identifiers

PMID24081450
PMCPMC3972372
OpenAlexW2048698029

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.