Evidence map›Paper›PMID 19151245›Full record

ArticleThe Journal of pharmacology and experimental therapeutics2009

KCNQ modulators reveal a key role for KCNQ potassium channels in regulating the tone of rat pulmonary artery smooth muscle.

Shreena Joshi, Vojtech Sedivy, Daniel Hodyc, Jan Herget, Alison M Gurney

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of pharmacology and experimental therapeutics, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

69 citing papers in PubMed, 113 citations in OpenAlex.

  1. Review
  2. Review
  3. Effects ofThe Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2025
    Article
  4. Article
  5. Acute Treatment with the M-Channel (KNeurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2023
    Article
  6. Review
  7. KCNQ5 activation by tannins mediates vasorelaxant effects of barks used in Native American botanical medicine.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2022
    Article
  8. Article
  9. KAmerican journal of physiology. Renal physiology · 2022
    Article
  10. Article
  11. Article
  12. Pharmacological Manipulation of KFrontiers in physiology · 2020
    Review
  13. Article
  14. Review
  15. Kv7 Channels in Lung Diseases.Frontiers in physiology · 2020
    Review
  16. Review
  17. Activation of KBritish journal of pharmacology · 2019
    Article
  18. Involvement of butyrate in electrogenic KPflugers Archiv : European journal of physiology · 2019
    Article
  19. Review
  20. Ion Channels in Pulmonary Hypertension: A Therapeutic Interest?International journal of molecular sciences · 2018
    Review

9 more citing papers are in PubMed but not listed here.

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.

Shreena JoshiFaculty of Life Sciences, University of Manchester, Manchester, UK.
Vojtech Sedivy
Daniel Hodyc
Jan Herget
Alison M Gurney
University of Manchester · GB

Funding

Biotechnology and Biological Sciences Research Council BBS/B/11761/2
6 · The paper itself

Abstract

Potassium channels are central to the regulation of pulmonary vascular tone. The smooth muscle cells of pulmonary artery display a background K(+) conductance with biophysical properties resembling those of KCNQ (K(V)7) potassium channels. Therefore, we investigated the expression and functional role of KCNQ channels in pulmonary artery. The effects of selective KCNQ channel modulators were investigated on K(+) current and membrane potential in isolated pulmonary artery smooth muscle cells (PASMCs), on the tension developed by intact pulmonary arteries, and on pulmonary arterial pressure in isolated perfused lungs and in vivo. The KCNQ channel blockers, linopirdine and XE991 [10,10-bis(4-pyridinylmethyl)-9(10H)-anthracenone], inhibited the noninactivating background K(+) conductance in PASMCs and caused depolarization, vasoconstriction, and raised pulmonary arterial pressure without constricting several systemic arteries or raising systemic pressure. The KCNQ channel openers, retigabine and flupirtine, had the opposite effects. PASMCs were found to express KCNQ4 mRNA, at higher levels than mesenteric artery, along with smaller amounts of KCNQ1 and 5. It is concluded that KCNQ channels, most probably KCNQ4, make an important contribution to the regulation of pulmonary vascular tone, with a greater contribution in pulmonary compared with systemic vessels. The pulmonary vasoconstrictor effect of KCNQ blockers is a potentially serious side effect, but the pulmonary vasodilator effect of the openers may be useful in the treatment of pulmonary hypertension.

Indexed as

AnimalsCell MembraneElectrophysiologyHemodynamicsIn Vitro TechniquesKCNQ Potassium ChannelsLungMaleMembrane PotentialsMuscle, Smooth, VascularMuscle TonusMyographyPatch-Clamp TechniquesPotassium Channel BlockersPulmonary ArteryRatsKCNQ Potassium ChannelsPotassium Channel BlockersRNA, Messenger

Identifiers

PMID19151245
PMCPMC2684066
OpenAlexW1979543489

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.