Evidence map›Paper›PMID 18195387›Full record

ArticleThe Journal of general physiology2008

Ca2+-activated K+ channels in murine endothelial cells: block by intracellular calcium and magnesium.

Jonathan Ledoux, Adrian D Bonev, Mark T Nelson

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of general physiology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

56 citing papers in PubMed, 96 citations in OpenAlex.

  1. Bilobalide increases SKBMC complementary medicine and therapies · 2026
    Article
  2. Guidelines for evaluating endothelial function in vascular tissue.American journal of physiology. Heart and circulatory physiology · 2026
    Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Dual effects of the small-conductance CaAmerican journal of physiology. Heart and circulatory physiology · 2023
    Article
  9. Article
  10. CaInternational journal of molecular sciences · 2023
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Impact of IBiophysical journal · 2020
    Article
  16. Review
  17. Calcium signals that determine vascular resistance.Wiley interdisciplinary reviews. Systems biology and medicine · 2019
    Review
  18. Review
  19. Article
  20. 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

3 authors at 1 institution in 1 country.

Jonathan LedouxDepartment of Pharmacology, College of Medicine, University of Vermont, Burlington 05405, USA.
Adrian D Bonev
Mark T Nelson
University of Vermont · US

Funding

VASCULAR DYSFUNCTION AS AN ETIOLOGY OF HYPERTENSIONP01HL077378 · NHLBI · TUFTS MEDICAL CENTER · PI MENDELSOHN, MICHAEL E · 2004 to 2008
$11.0M
REGULATION OF CEREBRAL ARTERY DILATIONR01HL044455 · NHLBI · UNIVERSITY OF VERMONT &ST AGRIC COLLEGE · PI NELSON, MARK T · 1991 to 2010
$3.9M
CORONARY ARTERY REGULATION BY CA2+SIGNALING &ESTROGENR01HL063722 · NHLBI · UNIVERSITY OF VERMONT &ST AGRIC COLLEGE · PI NELSON, MARK T · 2000 to 2003
$1.5M
NHLBI NIH HHS HL44455NHLBI NIH HHS HL63722NHLBI NIH HHS HL77378NHLBI NIH HHS P01 HL077378NHLBI NIH HHS R01 HL044455NHLBI NIH HHS R01 HL063722
6 · The paper itself

Abstract

The intermediate (IK(Ca)) and small (SK(Ca)) conductance Ca(2+)-sensitive K(+) channels in endothelial cells (ECs) modulate vascular diameter through regulation of EC membrane potential. However, contribution of IK(Ca) and SK(Ca) channels to membrane current and potential in native endothelial cells remains unclear. In freshly isolated endothelial cells from mouse aorta dialyzed with 3 microM free [Ca(2+)](i) and 1 mM free [Mg(2+)](i), membrane currents reversed at the potassium equilibrium potential and exhibited an inward rectification at positive membrane potentials. Blockers of large-conductance, Ca(2+)-sensitive potassium (BK(Ca)) and strong inward rectifier potassium (K(ir)) channels did not affect the membrane current. However, blockers of IK(Ca) channels, charybdotoxin (ChTX), and of SK(Ca) channels, apamin (Ap), significantly reduced the whole-cell current. Although IK(Ca) and SK(Ca) channels are intrinsically voltage independent, ChTX- and Ap-sensitive currents decreased steeply with membrane potential depolarization. Removal of intracellular Mg(2+) significantly increased these currents. Moreover, concomitant reduction of the [Ca(2+)](i) to 1 microM caused an additional increase in ChTX- and Ap-sensitive currents so that the currents exhibited theoretical outward rectification. Block of IK(Ca) and SK(Ca) channels caused a significant endothelial membrane potential depolarization (approximately 11 mV) and decrease in [Ca(2+)](i) in mesenteric arteries in the absence of an agonist. These results indicate that [Ca(2+)](i) can both activate and block IK(Ca) and SK(Ca) channels in endothelial cells, and that these channels regulate the resting membrane potential and intracellular calcium in native endothelium.

Indexed as

AlgorithmsAniline CompoundsAnimalsAortaApaminCalciumCells, CulturedCharybdotoxinElectrophysiologyEndothelial CellsEndothelium, VascularFemaleIntermediate-Conductance Calcium-Activated Potassium ChannelsIn Vitro TechniquesIon Channel GatingMagnesiumAniline CompoundsApaminCalciumCharybdotoxinFluo 4Intermediate-Conductance Calcium-Activated Potassium ChannelsKcnn3 protein, mouseKcnn4 protein, mouseMagnesiumPotassium Channels, Calcium-ActivatedPotassium ChlorideSmall-Conductance Calcium-Activated Potassium ChannelsXanthenes

Identifiers

PMID18195387
PMCPMC2213563
OpenAlexW2162655920

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.