Evidence map›Paper›PMID 16446508›Full record

ArticleThe Journal of general physiology2006

A Na+- and Cl- -activated K+ channel in the thick ascending limb of mouse kidney.

Marc Paulais, Sahran Lachheb, Jacques Teulon

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The Journal of general physiology, 2006. 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
1.0field-weighted citation impact, top 28% 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, 52 citations in OpenAlex.

  1. Andrology · 2025
    Review
  2. Role of calcineurin in regulating renal potassium (KActa physiologica (Oxford, England) · 2024
    Review
  3. Inwardly rectifying KAmerican journal of physiology. Cell physiology · 2022
    Review
  4. Review
  5. ClAmerican journal of physiology. Cell physiology · 2020
    Review
  6. Kir4.1/Kir5.1 in the DCT plays a role in the regulation of renal KAmerican journal of physiology. Renal physiology · 2019
    Article
  7. Review
  8. Epithelial transport inThe Journal of general physiology · 2017
    Review
  9. Review
  10. Review
  11. Review
  12. Article
  13. The expression, regulation, and function of Kir4.1 (Kcnj10) in the mammalian kidney.American journal of physiology. Renal physiology · 2016
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  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 1 institution in 1 country.

Marc PaulaisUPMC, CNRS UMR7134, Institut Fédératif de Recherches 58, Paris, France. Marc.Paulais@bhdc.jussieu.fr
Sahran Lachheb
Jacques Teulon
Centre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study investigates the presence and properties of Na+-activated K+ (K(Na)) channels in epithelial renal cells. Using real-time PCR on mouse microdissected nephron segments, we show that Slo2.2 mRNA, which encodes for the K(Na) channels of excitable cells, is expressed in the medullary and cortical thick ascending limbs of Henle's loop, but not in the other parts of the nephron. Patch-clamp analysis revealed the presence of a high conductance K+ channel in the basolateral membrane of both the medullary and cortical thick ascending limbs. This channel was highly K+ selective (P(K)/P(Na) approximately 20), its conductance ranged from 140 to 180 pS with subconductance levels, and its current/voltage relationship displayed intermediate, Na+-dependent, inward rectification. Internal Na+ and Cl- activated the channel with 50% effective concentrations (EC50) and Hill coefficients (nH) of 30 +/- 1 mM and 3.9 +/- 0.5 for internal Na+, and 35 +/- 10 mM and 1.3 +/- 0.25 for internal Cl-. Channel activity was unaltered by internal ATP (2 mM) and by internal pH, but clearly decreased when internal free Ca2+ concentration increased. This is the first demonstration of the presence in the epithelial cell membrane of a functional, Na+-activated, large-conductance K+ channel that closely resembles native K(Na) channels of excitable cells. This Slo2.2 type, Na+- and Cl--activated K+ channel is primarily located in the thick ascending limb, a major renal site of transcellular NaCl reabsorption.

Indexed as

Adenosine TriphosphateAnimalsCell MembraneChloridesEpithelial CellsHydrogen-Ion ConcentrationLarge-Conductance Calcium-Activated Potassium ChannelsLoop of HenleMaleMiceMice, Inbred StrainsNerve Tissue ProteinsPatch-Clamp TechniquesPotassium ChannelsPotassium Channels, Sodium-ActivatedReverse Transcriptase Polymerase Chain ReactionAdenosine TriphosphateChloridesLarge-Conductance Calcium-Activated Potassium ChannelsNerve Tissue ProteinsPotassium ChannelsPotassium Channels, Sodium-ActivatedRNA, MessengerSlo2 protein, mouseSodium

Identifiers

PMID16446508
PMCPMC2151493
OpenAlexW1968522838

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.