Evidence map›Paper›PMID 26277265›Full record

ArticleBiochimica et biophysica acta2015

Unoprostone activation of BK (KCa1.1) channel splice variants.

Ling Yu, Amity F Eaton, Qiang Yue, Hui-Fang Bao, He-Ping Ma, John Cuppoletti, Douglas C Eaton

Abstract read
In one paragraph

Article in Biochimica et biophysica acta, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.5field-weighted citation impact, top 33% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. BK Channels in the Central Nervous System.International review of neurobiology · 2016
    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

7 authors at 3 institutions in 2 countries.

Ling YuCollege of Resources and Environmental Sciences, Nanjing Agricultural University, Nanjing 210095, China.
Amity F EatonDepartment of Physiology and the Center for Cell and Molecular Signaling, Emory University School of Medicine Atlanta, GA 30322, United States.
Qiang YueDepartment of Physiology and the Center for Cell and Molecular Signaling, Emory University School of Medicine Atlanta, GA 30322, United States.
Hui-Fang BaoDepartment of Physiology and the Center for Cell and Molecular Signaling, Emory University School of Medicine Atlanta, GA 30322, United States.
He-Ping MaDepartment of Physiology and the Center for Cell and Molecular Signaling, Emory University School of Medicine Atlanta, GA 30322, United States.
John CuppolettiDepartment of Molecular and Cellular Physiology, University of Cincinnati, Cincinnati, OH 45267, USA.
Douglas C EatonDepartment of Physiology and the Center for Cell and Molecular Signaling, Emory University School of Medicine Atlanta, GA 30322, United States. Electronic address: deaton@emory.edu.
Emory University · USNanjing Agricultural University · CNUniversity of Cincinnati · US

Funding

IRACDA Fellowships in Research and Science Training (FIRST)K12GM000680 · NIGMS · EMORY UNIVERSITY · PI BROWN, LOU ANN S, MCCARTY, NAEL A · 2000 to 2024
$41.2M
REGULATION OF SODIUM IN TIGHT EPITHELIAR37DK037963 · NIDDK · EMORY UNIVERSITY · PI EATON, DOUGLAS C. · 2002 to 2011
$3.8M
Role of Ion Channels in Kidney DiseasesR01DK100582 · NIDDK · EMORY UNIVERSITY · PI MA, HE-PING · 2014 to 2017
$1.4M
NIDDK NIH HHS R01 DK100582NIDDK NIH HHS R37 DK037963NIDDK NIH HHS R37DK037963NIGMS NIH HHS K12 GM000680
6 · The paper itself

Abstract

This investigation was conducted to study the relationship between intracellular Ca(2+) and activation of large conductance Ca(2+)-activated K(+) (BK) currents by unoprostone, the first synthetic docosanoid. We used HEK293 cells stably transfected with two BK channel splice variants, one sensitive to unoprostone and the other insensitive. We examined the effects of unoprostone on channel activity in excised inside-out patches and cell-attached patches. The half-maximal stimulation of the sensitive BK channels by Ca(2+) was shifted from 3.4±0.017 nM to 0.81±.0058 nM in the presence of 10 nM unoprostone. There was no effect on insensitive channels even at unoprostone concentrations as high as 1000 nM. There was no effect of unoprostone on the voltage dependence of the BK channels. Changes in open probability and effects of Ca(2+) and unoprostone were best described by a synergistic binding model. These data would suggest that Ca(2+) and unoprostone were binding to sites close to one another on the channel protein and that unoprostone binding causes the affinity of the calcium binding site to increase. This idea is consistent with three dimensional models of the Ca(2+) binding site and a putative unoprostone binding domain. Our results have important implications for the clinical use of unoprostone to activate BK channels. Channel activation will be limited if intracellular Ca(2+) is not elevated.

Indexed as

Alternative SplicingAmino Acid SequenceAnimalsCalciumDinoprostDose-Response Relationship, DrugHEK293 CellsHumansIntracellular SpaceIon Channel GatingLarge-Conductance Calcium-Activated Potassium Channel alpha SubunitsMembrane PotentialsMolecular Sequence DataPatch-Clamp TechniquesProtein IsoformsRatsCalciumDinoprostisopropyl unoprostoneKcnma1 protein, ratLarge-Conductance Calcium-Activated Potassium Channel alpha SubunitsProtein IsoformsBK channelsCa(2+)-dependenceKCNMA1Rescula®Single channelsUnoprostone

Identifiers

PMID26277265
PMCPMC4598293
OpenAlexW2208722776

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.