Evidence map›Paper›PMID 17091215›Full record

ArticleThe Journal of membrane biology2006

A Kir2.3-like K+ conductance in mouse cortical collecting duct principal cells.

I D Millar, H C Taylor, G J Cooper, J D Kibble, L Robson

Abstract read
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In one paragraph

Article in The Journal of membrane biology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.4field-weighted citation impact, top 40% 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

6 citing papers in PubMed, 13 citations in OpenAlex.

  1. Expression, localization, and functional properties of inwardly rectifying KAmerican journal of physiology. Renal physiology · 2020
    Review
  2. Role and mechanisms of regulation of the basolateral KActa physiologica (Oxford, England) · 2017
    Review
  3. Review
  4. Article
  5. Basolateral membrane K+ channels in renal epithelial cells.American journal of physiology. Renal physiology · 2012
    Review
  6. 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 2 institutions in 2 countries.

I D MillarDepartment of Biomedical Science, University of Sheffield, Sheffield S10 2TN, United Kingdom.
H C Taylor
G J Cooper
J D Kibble
L Robson
University of Sheffield · GBSt. George's University · GD

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

K(+) channels play an important role in renal collecting duct cell function. The current study examined barium (Ba(2+))-sensitive whole-cell K(+) currents (IKBa) in mouse isolated collecting duct principal cells. IKBa demonstrated strong inward rectification and was inhibited by Ba(2+) in a dose- and voltage-dependent fashion, with the K (d) decreasing with hyperpolarization. The electrical distance of block by Ba(2+) was around 8.5%. As expected for voltage-dependent inhibition, the association constant increased with hyperpolarization, suggesting that the rate of Ba(2+) entry was increased at negative potentials. The dissociation constant also increased with hyperpolarization, consistent with the movement of Ba(2+) ions into the intracellular compartment at negative potentials. These properties are not consistent with ROMK but are consistent with the properties of Kir2.3. Kir2.3 is thought to be the dominant basolateral K(+) channel in principal cells. This study provides functional evidence for the expression of Kir2.3 in mouse cortical collecting ducts and confirms the expression of Kir2.3 in this segment of the renal tubule using reverse-transcriptase polymerase chain reaction. The conductance described here is the first report of a macroscopic K(+) conductance in mouse principal cells that shares the biophysical profile of Kir2.3. The properties and dominant nature of the conductance suggest that it plays an important role in K(+) handling in the principal cells of the cortical collecting duct.

Indexed as

AnimalsBariumDose-Response Relationship, DrugElectric ConductivityEpithelial Sodium ChannelsFemalegamma-GlutamyltransferaseGene ExpressionKidney CortexKidney Tubules, CollectingMaleMembrane PotentialsMiceMice, Inbred C57BLMucoproteinsPatch-Clamp TechniquesBariumEpithelial Sodium Channelsgamma-GlutamyltransferaseKcnj4 protein, mouseMucoproteinsPotassium Channels, Inwardly RectifyingPotassium ChlorideSodium ChlorideSodium Chloride SymportersUmod protein, mouseUromodulin

Identifiers

PMID17091215
OpenAlexW1987864325

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.