Evidence map›Paper›PMID 24591572›Full record

ArticleThe Journal of physiology2014

Increase in cytosolic Ca2+ produced by hypoxia and other depolarizing stimuli activates a non-selective cation channel in chemoreceptor cells of rat carotid body.

Dawon Kang, Jiaju Wang, James O Hogan, Rudi Vennekens, Marc Freichel, Carl White, Donghee Kim

Open access · greenAbstract read
In one paragraph

Article in The Journal of physiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

18 citing papers in PubMed, 27 citations in OpenAlex.

  1. Acute Hypoxia Inhibits KActa physiologica (Oxford, England) · 2026
    Article
  2. Article
  3. TASK inhibition by mild acidosis increases CaAmerican journal of physiology. Lung cellular and molecular physiology · 2023
    Article
  4. Article
  5. Review
  6. CaAmerican journal of physiology. Cell physiology · 2020
    Article
  7. Review
  8. Article
  9. Activation of voltage-dependent KThe Journal of physiology · 2018
    Article
  10. All for one - OThe Journal of physiology · 2018
    Article
  11. Review
  12. Is Carotid Body Physiological OFrontiers in physiology · 2018
    Review
  13. Article
  14. Article
  15. Carotid body oxygen sensing and adaptation to hypoxia.Pflugers Archiv : European journal of physiology · 2016
    Review
  16. TASK channels in arterial chemoreceptors and their role in oxygen and acid sensing.Pflugers Archiv : European journal of physiology · 2015
    Review
  17. Role of K₂p channels in stimulus-secretion coupling.Pflugers Archiv : European journal of physiology · 2015
    Review
  18. Oxygen sensing with ion channels.Channels (Austin, Tex.) · 2014
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 4 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. donghee.kim@rosalindfranklin.edu.
Jiaju Wang
James O Hogan
Rudi Vennekens
Marc Freichel
Carl White
Donghee Kim
Rosalind Franklin University of Medicine and Science · USHeidelberg University · DEKU Leuven · BE

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 HL111497NHLBI NIH HHS R01 HL111497
6 · The paper itself

Abstract

The current model of O2 sensing by carotid body chemoreceptor (glomus) cells is that hypoxia inhibits the outward K(+) current and causes cell depolarization, Ca(2+) influx via voltage-dependent Ca(2+) channels and a rise in intracellular [Ca(2+)] ([Ca(2+)]i). Here we show that hypoxia (<5% O2), in addition to inhibiting the two-pore domain K(+) channels TASK-1/3 (TASK), indirectly activates an ∼20 pS channel in isolated glomus cells. The 20 pS channel was permeable to K(+), Na(+) and Cs(+) but not to Cl(-) or Ca(2+). The 20 pS channel was not sensitive to voltage. Inhibition of TASK by external acid, depolarization of glomus cells with high external KCl (20 mm) or opening of the Ca(2+) channel with FPL64176 activated the 20 pS channel when 1 mm Ca(2+) was present in the external solution. Ca(2+) (10 μm) applied to the cytosolic side of inside-out patches activated the 20 pS channel. The threshold [Ca(2+)]i for activation of the 20 pS channel in cell-attached patches was ∼200 nm. The reversal potential of the 20 pS channel was estimated to be -28 mV. Our results reveal a sequential mechanism in which hypoxia (<5% O2) first inhibits the K(+) conductance and then activates a Na(+)-permeable, non-selective cation channel via depolarization-induced rise in [Ca(2+)]i. Our results suggest that inhibition of K(+) efflux and stimulation of Na(+) influx both contribute to the depolarization of glomus cells during moderate to severe hypoxia.

Indexed as

AnimalsCalciumCarotid BodyCell HypoxiaChemoreceptor CellsCytosolFemaleMaleMiceMice, Inbred C57BLMice, KnockoutNerve Tissue ProteinsPotassium Channels, Tandem Pore DomainRatsRats, Sprague-DawleyCalciumNerve Tissue ProteinsPotassium Channels, Tandem Pore Domainpotassium channel subfamily K member 3

Identifiers

PMID24591572
PMCPMC4230773
OpenAlexW1539356845

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.