Evidence map›Paper›PMID 10766916›Full record

ArticleThe Journal of physiology2000

Pregnancy switches adrenergic signal transduction in rat and human uterine myocytes as probed by BKCa channel activity.

X B Zhou, G X Wang, B Huneke, T Wieland, M Korth

Open access · greenAbstract read
In one paragraph

Article in The Journal of physiology, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

15 citing papers in PubMed, 37 citations in OpenAlex.

  1. Noradrenergic αMolecular neurobiology · 2025
    Article
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  13. MaxiK channel partners: physiological impact.The Journal of physiology · 2006
    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

5 authors at 1 institution in 1 country.

X B ZhouInstitut fur Experimentelle und Klinische Pharmakologie und Toxikologie, und Frauenklinik, Universitats-Krankenhaus Eppendorf, Martinistrasse 52, D-20246 Hamburg, Germany.
G X Wang
B Huneke
T Wieland
M Korth
Olgahospital · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

1. We used large conductance Ca2+-activated K+ (BKCa) channel activity as a probe to characterize the inhibitory/stimulatory G protein (Gi/Gs) signalling pathways in intact cells from pregnant (PM) and non-pregnant (NPM) myometrium. 2. Isoprenaline (10 microM) enhanced the outward current (Iout) in PM cells and inhibited Iout in NPM cells. Additional application of the alpha2-adrenoceptor (alpha2-AR) agonist clonidine (10 microM) further enhanced the isoprenaline-modulated Iout in PM cells but partially antagonized Iout in NPM cells. Clonidine alone did not affect Iout. The specific cAMP kinase (PKA) inhibitor H-89 (1 microM) abolished the effects of isoprenaline and clonidine. The specific BKCa channel blocker iberiotoxin (0.1 microM) inhibited Iout by approximately 80 %; the residual current was insensitive to isoprenaline. 3. Inhibition of Gi activity by either pertussis toxin or the GTPase activating protein RGS16 abolished inhibitory as well as stimulatory effects of clonidine on Iout. 4. Transducin-alpha, a scavenger of Gi betagamma dimers, converted the stimulatory action of clonidine on Iout into an inhibitory effect. Free transducin-betagamma enhanced both the stimulatory and the inhibitory effects of isoprenaline on Iout. 5. The results demonstrate that BKCa channel activity is a sensitive probe to follow adenylyl cyclase-cAMP-PKA signalling in myometrial smooth muscle cells. Both Gialpha-mediated inhibition and Gibetagamma-mediated stimulation can occur in the same cell, irrespective of pregnancy. It is speculated that the coupling between alpha2-AR and Gi proteins is more efficient during pregnancy and that Gibetagamma at high levels simply override the inhibitory action of Gi alpha.

Indexed as

Potassium Channels, Calcium-ActivatedAdenylyl CyclasesAdrenergic alpha-2 Receptor AgonistsAdrenergic alpha-AgonistsAdrenergic beta-AgonistsAnimalsCalciumCell MembraneCyclic AMPFemaleHumansIn Vitro TechniquesLarge-Conductance Calcium-Activated Potassium ChannelsMembrane PotentialsMuscle, SmoothPatch-Clamp TechniquesAdenylyl CyclasesAdrenergic alpha-2 Receptor AgonistsAdrenergic alpha-AgonistsAdrenergic beta-AgonistsCalciumCyclic AMPLarge-Conductance Calcium-Activated Potassium ChannelsPotassium ChannelsPotassium Channels, Calcium-ActivatedReceptors, Adrenergic, alpha-2Receptors, Adrenergic, beta

Identifiers

PMID10766916
PMCPMC2269869
OpenAlexW2160414361

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.