Evidence map›Paper›PMID 12684258›Full record

ArticleBritish journal of pharmacology2003

Inhibition of EDHF by two new combinations of K+-channel inhibitors in rat isolated mesenteric arteries.

Jane M Hinton, Philip D Langton

Open access · bronzeAbstract read
In one paragraph

Article in British journal of pharmacology, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.2field-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

25 citing papers in PubMed, 60 citations in OpenAlex.

  1. Article
  2. Reduced membrane cholesterol after chronic hypoxia limits Orai1-mediated pulmonary endothelial CaAmerican journal of physiology. Heart and circulatory physiology · 2018
    Article
  3. Article
  4. Reduced membrane cholesterol limits pulmonary endothelial CaAmerican journal of physiology. Heart and circulatory physiology · 2017
    Article
  5. Article
  6. Article
  7. Role of in vivo vascular redox in resistance arteries.Hypertension (Dallas, Tex. : 1979) · 2015
    Article
  8. Review
  9. Mechanisms of enhanced basal tone of brain parenchymal arterioles during early postischemic reperfusion: role of ET-1-induced peroxynitrite generation.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2013
    Article
  10. Article
  11. Novel role of endothelial BKCa channels in altered vasoreactivity following hypoxia.American journal of physiology. Heart and circulatory physiology · 2010
    Article
  12. ESCRT-dependent targeting of plasma membrane localized KCa3.1 to the lysosomes.American journal of physiology. Cell physiology · 2010
    Article
  13. Article
  14. Article
  15. A key role for Na+/K+-ATPase in the endothelium-dependent oscillatory activity of mouse small mesenteric arteries.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2009
    Article
  16. Article
  17. Article
  18. Article
  19. Article
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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

2 authors at 1 institution in 1 country.

Jane M HintonDepartment of Physiology, School of Medical Sciences, University of Bristol, Bristol BS8 1TD, UK. J.Hinton@bristol.ac.uk
Philip D Langton
University of Bristol · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is widely established that in rat mesenteric arteries, endothelium-derived hyperpolarizing factor (EDHF)-mediated relaxation evoked by acetylcholine is abolished by a combination of charybdotoxin plus apamin. 4-Aminopyridine, an inhibitor of voltage-gated (Kv) K(+)-channels, in combination with apamin had moderate effects on the EDHF-mediated relaxation. Maurotoxin (MTX), an inhibitor of Kv and intermediate-conductance Ca(2+)-activated K(+)-channels (IK), had no effect on EDHF-mediated relaxation. However, MTX in combination with apamin completely abolished EDHF-mediated relaxation and endothelial cell hyperpolarization. The selective IK inhibitor 2-(2-chlorophenyl)-2,2-diphenyl acetonitrile (TRAM-39) had no significant effect on EDHF-mediated relaxation. EDHF-mediated vasorelaxation and hyperpolarization was abolished by a combination of TRAM-39 and apamin. These data demonstrate two new combinations of K(+)-channel inhibitors for the investigation of EDHF. Furthermore, by using TRAM-39, a potent selective inhibitor of IK channels, we provide the first direct evidence that abolition of EDHF requires the simultaneous presence of intermediate- and small-conductance Ca(2+)-activated K(+)-channel inhibitors.

Indexed as

4-AminopyridineAcetonitrilesAnimalsApaminBenzimidazolesBiological FactorsCharybdotoxinDose-Response Relationship, DrugMaleMesenteric ArteriesPotassium Channels, Calcium-ActivatedPotassium Channels, Voltage-GatedRatsRats, WistarScorpionsScorpion Venoms1-ethyl-2-benzimidazolinone(2-Chlorophenyl)(diphenyl)acetonitrile4-AminopyridineAcetonitrilesApaminBenzimidazolesBiological FactorsCharybdotoxinendothelium-dependent hyperpolarization factormaurotoxinPotassium Channels, Calcium-ActivatedPotassium Channels, Voltage-GatedScorpion VenomsTriphenylmethyl Compounds

Identifiers

PMID12684258
PMCPMC1573761
OpenAlexW1987821977

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.