Evidence map›Paper›PMID 25474527›Full record

ArticlePloS one2014

Computational modeling reveals key contributions of KCNQ and hERG currents to the malleability of uterine action potentials underpinning labor.

Wing-Chiu Tong, Rachel M Tribe, Roger Smith, Michael J Taggart

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

11 citing papers in PubMed, 23 citations in OpenAlex.

  1. KCommunications medicine · 2026
    Article
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  4. An update on pacemaking in the myometrium.The Journal of physiology · 2026
    Review
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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 3 institutions in 2 countries.

Wing-Chiu TongInstitute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom.
Rachel M TribeDivision of Women's Health, King's College London and King's Health Partners, London, United Kingdom.
Roger SmithHunter Medical Research Institute, University of Newcastle, New Lambton, New South Wales, Australia.
Michael J TaggartInstitute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom.
Newcastle University · GBHunter Medical Research Institute · AUKings Health Partners · GB

Funding

Medical Research Council G0900525Medical Research Council G0902091Medical Research Council G1100243
6 · The paper itself

Abstract

The electrical excitability of uterine smooth muscle cells is a key determinant of the contraction of the organ during labor and is manifested by spontaneous, periodic action potentials (APs). Near the end of term, APs vary in shape and size reflecting an ability to change the frequency, duration and amplitude of uterine contractions. A recent mathematical model quantified several ionic features of the electrical excitability in uterine smooth muscle cells. It replicated many of the experimentally recorded uterine AP configurations but its limitations were evident when trying to simulate the long-duration bursting APs characteristic of labor. A computational parameter search suggested that delayed rectifying K(+) currents could be a key model component requiring improvement to produce the longer-lasting bursting APs. Of the delayed rectifying K(+) currents family it is of interest that KCNQ and hERG channels have been reported to be gestationally regulated in the uterus. These currents exhibit features similar to the broadly defined uterine IK1 of the original mathematical model. We thus formulated new quantitative descriptions for several I(KCNQ) and I(hERG). Incorporation of these currents into the uterine cell model enabled simulations of the long-lasting bursting APs. Moreover, we used this modified model to simulate the effects of different contributions of I(KCNQ) and I(hERG) on AP form. Our findings suggest that the alterations in expression of hERG and KCNQ channels can potentially provide a mechanism for fine tuning of AP forms that lends a malleability for changing between plateau-like and long-lasting bursting-type APs as uterine cells prepare for parturition.

Indexed as

Action PotentialsComputer SimulationModels, BiologicalEther-A-Go-Go Potassium ChannelsFemaleHumansKCNQ Potassium ChannelsKineticsLabor, ObstetricMyocytes, Smooth MusclePregnancyUterusEther-A-Go-Go Potassium ChannelsKCNQ Potassium Channels

Identifiers

PMID25474527
PMCPMC4256391
OpenAlexW2055991741

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.