Evidence map›Paper›PMID 10200419›Full record

ArticleThe Journal of physiology1999

Effects of intra- and extracellular acidifications on single channel Kir2.3 currents.

G Zhu, S Chanchevalap, N Cui, C Jiang

Open access · greenAbstract read
In one paragraph

Article in The Journal of physiology, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

25 citing papers in PubMed, 72 citations in OpenAlex.

  1. Comparison of KHandbook of experimental pharmacology · 2021
    Article
  2. Review
  3. Article
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  5. Article
  6. Article
  7. Article
  8. Modulation of acid-sensing ion channels: molecular mechanisms and therapeutic potential.International journal of physiology, pathophysiology and pharmacology · 2011
    Article
  9. The locus coeruleus and central chemosensitivity.Respiratory physiology & neurobiology · 2010
    Review
  10. Article
  11. TASK channels contribute to the K+-dominated leak current regulating respiratory rhythm generation in vitro.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2010
    Article
  12. SAP97 regulates Kir2.3 channels by multiple mechanisms.American journal of physiology. Heart and circulatory physiology · 2009
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
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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

4 authors at 1 institution in 1 country.

G ZhuDepartment of Biology, Georgia State University, 24 Peachtree Center Avenue, Atlanta, GA 30303-4010, USA.
S Chanchevalap
N Cui
C Jiang
Georgia State University · US

Funding

KIR channel modulations in hypercapnic acidosisR01HL058410 · NHLBI · GEORGIA STATE UNIVERSITY · PI JIANG, CHUN · 1996 to 2004
$1.0M
NHLBI NIH HHS R01 HL058410NHLBI NIH HHS R01 HL58410-01
6 · The paper itself

Abstract

1. The inward rectifier K+ channel Kir2.3 is inhibited by hypercapnia, and this inhibition may be mediated by decreases in intra- and extracellular pH. To understand whether Kir2.3 has two distinct pH sensors and whether cytosol-soluble factors are involved in the modulation of this channel during intracellular acidification, single channel currents were studied by expressing Kir2.3 in Xenopus oocytes. 2. In excised inside-out patches, Kir2.3 currents had a high baseline channel open-state probability (Po, at pH 7.4) with a strong inward rectification. Single channel conductance at hyperpolarizing membrane potential was about 17 pS with 150 mM K+ applied to both sides of the membrane. The channel showed a substate conductance of about 8 pS. 3. Reduction of intracellular pH (pHi) produced a fast and reversible inhibition of single channel Kir2.3 currents in inside-out patches. The extent of this inhibition is concentration dependent. A clear reduction in Kir2.3 currents was seen at pHi 7.0, and channel activity was completely suppressed at pHi 6.2 with mid-point inhibition (pK) at pH 6.77. 4. The effect of low pHi on Kir2.3 currents was due to a strong inhibition of Po and a moderate suppression of single channel conductance. The pK values for these single channel properties were pH 6.78 and 6.67, respectively. 5. The decrease in Po with low pHi resulted from an increase in the channel mean closed time without significant changes in the mean open time. Substate conductance was not seen during low pHi. 6. Decrease in extracellular pH (pHo) also caused inhibition of single channel activity of Kir2.3 currents in excised outside-out patches. This effect, however, was clearly different from that of pHi: the pK (pH 6.70) was about 0.1 pH units lower; more than 50 % channel activity was retained at pHo 5.8; and low pHo affected mainly single channel conductance. 7. These results therefore indicate that (1) there are two distinct pH sensors in Kir2.3, (2) different mechanisms are involved in the modulation of Kir2.3 through these two pH sensors, and (3) cytosol-soluble factors do not appear to be engaged in this modulation.

Indexed as

Potassium Channels, Inwardly RectifyingAlgorithmsAnimalsCytosolElectrophysiologyFemaleHydrogen-Ion ConcentrationIon Channel GatingMembrane PotentialsOocytesPatch-Clamp TechniquesPotassium ChannelsXenopus laevisKCNJ4 protein, humanPotassium ChannelsPotassium Channels, Inwardly Rectifying

Identifiers

PMID10200419
PMCPMC2269286
OpenAlexW2147869977

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.