Evidence map›Paper›PMID 19074509›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2009

Openers of SKCa and IKCa channels enhance agonist-evoked endothelial nitric oxide synthesis and arteriolar vasodilation.

Jian-zhong Sheng, Srikanth Ella, Michael J Davis, Michael A Hill, Andrew P Braun

Open access · greenAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
3.5field-weighted citation impact, top 8% 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

49 citing papers in PubMed, 85 citations in OpenAlex.

  1. Article
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  3. Administration of the KFrontiers in pharmacology · 2025
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  5. CaInternational journal of molecular sciences · 2023
    Review
  6. Review
  7. Subtype-Selective Positive Modulation of KACS chemical biology · 2022
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Internalization and Transportation of Endothelial Cell Surface KOxidative medicine and cellular longevity · 2019
    Article
  15. AlphaPhysiological reports · 2018
    Article
  16. Pharmacologic targeting of endothelial CaChannels (Austin, Tex.) · 2018
    Review
  17. Impact of Aging on Calcium Signaling and Membrane Potential in Endothelium of Resistance Arteries: A Role for Mitochondria.The journals of gerontology. Series A, Biological sciences and medical sciences · 2017
    Article
  18. Article
  19. Article
  20. Direct activation of CaEuropean journal of pharmacology · 2017
    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.

Jian-zhong ShengDepartment of Pharmacology and Therapeutics, University of Calgary, Calgary, Alberta, Canada.
Srikanth Ella
Michael J Davis
Michael A Hill
Andrew P Braun
University of Missouri · USLibin Cardiovascular Institute of Alberta · CA

Funding

PHS HHS NHLBI-71796
6 · The paper itself

Abstract

Recent data have led us to hypothesize that selective activation of endothelial small- and/or intermediate-conductance, calcium-activated potassium channels (SK(Ca) and IK(Ca) channels, respectively) by the opener compounds NS309 and DCEBIO would augment stimulated nitric oxide (NO) synthesis and vasodilation in resistance arteries. Experimentally, ATP-evoked changes in membrane potential, cytosolic Ca(2+), and NO synthesis were recorded by patch clamp and microfluorimetry in single human endothelial cells. Agonist-evoked inhibition of myogenic tone in isolated, pressurized arterioles from rat cremaster skeletal muscle was analyzed by video microscopy. NS309 and DCEBIO enhanced ATP-evoked membrane hyperpolarization and cytosolic Ca(2+) transients, along with acute NO synthesis in isolated endothelial cells. The acetylcholine-mediated inhibition of myogenic tone (IC(50)=237 nM) was left-shifted in the presence of NS309 and DCEBIO (10, 100, and 1000 nM) to IC(50) values of 101, 78, and 43 nM; endothelial denudation inhibited this drug effect. L-NAME attenuated the acetylcholine-induced inhibition of myogenic tone but did not interfere with NS309 and DCEBIO-evoked vasodilation. Collectively, our data demonstrate that drug-induced enhancement of endothelial SK(Ca) and IK(Ca) channel activities represents a novel cellular mechanism to increase vasodilation of small-resistance arterioles, thereby highlighting these channels as potential therapeutic targets in cardiovascular disease states associated with compromised NO signaling.

Indexed as

AcetylcholineAdenosine TriphosphateAnimalsArteriolesBenzimidazolesCalciumCell LineCytosolDose-Response Relationship, DrugEndothelial CellsEthylaminesFluoresceinsFluorometryHumansIndolesInhibitory Concentration 503-amino-4-monomethylamino-2',7'-difluorofluorecein5,6-dichloro-1-ethyl-1,3-dihydro-2H-benzimidazol-2-one6,7-dichloro-1H-indole-2,3-dione 3-oximeAcetylcholineAdenosine TriphosphateBenzimidazolesCalciumEthylaminesFluoresceinsIndolesNG-Nitroarginine Methyl EsterNitric OxideOximesPotassium Channels, Calcium-ActivatedSmall-Conductance Calcium-Activated Potassium Channels

Identifiers

PMID19074509
PMCPMC2660645
OpenAlexW2039867038

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.