Evidence map›Paper›PMID 20729401›Full record

ArticleAmerican journal of physiology. Heart and circulatory physiology2010

Sphingosine-1-phosphate prevents permeability increases via activation of endothelial sphingosine-1-phosphate receptor 1 in rat venules.

Gengqian Zhang, Sulei Xu, Yan Qian, Pingnian He

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Heart and circulatory physiology, 2010. 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
2.4field-weighted citation impact, top 11% 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, 48 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Cortical Actin Dynamics in Endothelial Permeability.Current topics in membranes · 2018
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Sphingosine-1-phosphate protects endothelial glycocalyx by inhibiting syndecan-1 shedding.American journal of physiology. Heart and circulatory physiology · 2014
    Article
  13. Article
  14. Microvascular permeability to water is independent of shear stress, but dependent on flow direction.American journal of physiology. Heart and circulatory physiology · 2013
    Article
  15. Tonic regulation of vascular permeability.Acta physiologica (Oxford, England) · 2013
    Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Review
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

4 authors at 1 institution in 2 countries.

Gengqian ZhangDepartment of Physiology and Pharmacology, School of Medicine, West Virginia University, Morgantown, West Virginia 26506-9229, USA.
Sulei Xu
Yan Qian
Pingnian He
West Virginia University · US

Funding

CELLULAR MODULATION OF MICROVESSEL PERMEABILITY IN VIVOR01HL056237 · NHLBI · WEST VIRGINIA UNIVERSITY · PI HE, PINGNIAN · 2001 to 2013
$3.1M
Nitric Oxide and Microvessel Permeability In VivoR01HL084338 · NHLBI · WEST VIRGINIA UNIVERSITY · PI HE, PINGNIAN · 2007 to 2011
$1.6M
CELLULAR MODULATION OF MICROVESSEL PERMEABILITY IN VIVOR29HL056237 · NHLBI · UNIVERSITY OF CALIFORNIA DAVIS · PI HE, PINGNIAN · 1997 to 2001
$121k
NHLBI NIH HHS HL-084338NHLBI NIH HHS HL-56237NHLBI NIH HHS R01 HL056237NHLBI NIH HHS R01 HL084338
6 · The paper itself

Abstract

Sphingosine-1-phosphate (S1P) has been demonstrated to enhance endothelial barrier function in vivo and in vitro. However, different S1P receptor subtypes have been indicated to play different or even opposing roles in the regulation of vascular barrier function. This study aims to differentiate the roles of endogenous endothelial S1P subtype receptors in the regulation of permeability in intact microvessels using specific receptor agonist and antagonists. Microvessel permeability was measured with hydraulic conductivity (L(p)) in individually perfused rat mesenteric venules. S1P-mediated changes in endothelial intracellular Ca(2+) concentration ([Ca(2+)](i)) was measured in fura-2-loaded venules. Confocal images of fluorescent immunostaining illustrated the spatial expressions of three S1P subtype receptors (S1P(R1-3)) in rat venules. The application of S1P (1 μM) in the presence of S1P(R1-3) inhibited platelet-activating factor- or bradykinin-induced permeability increase. This S1P effect was reversed only with a selective S1P(R1) antagonist, W-146, and was not affected by S1P(R2) or S1P(R3) antagonists JTE-013 and CAY-10444, respectively. S1P(R1) was also identified as the sole receptor responsible for S1P-mediated increases in endothelial [Ca(2+)](i). S1P(R2) or S1P(R3) antagonist alone affected neither basal L(p) nor platelet-activating factor-induced permeability increase. The selective S1P(R1) agonist, SEW-2871, showed similar [Ca(2+)](i) and permeability effect to that of S1P. These results indicate that, despite the presence of S1P(R1-3) in the intact venules, only the activation of endothelial S1P(R1) is responsible for the protective action of S1P on microvessel permeability and that endogenous S1P(R2) or S1P(R3) did not exhibit functional roles in the regulation of permeability under basal or acutely stimulated conditions.

Indexed as

AnilidesAnimalsCalciumCapillary PermeabilityEndothelium, VascularFemaleLysophospholipidsMesenteryModels, AnimalOrganophosphonatesPyrazolesPyridinesRatsRats, Sprague-DawleyReceptors, LysosphingolipidSphingosine3-amino-4-(3-hexylphenylamino)-4-oxobutylphosphonic acidAnilidesCalciumJTE 013LysophospholipidsOrganophosphonatesPyrazolesPyridinesReceptors, LysosphingolipidSphingosinesphingosine 1-phosphate

Identifiers

PMID20729401
PMCPMC2993214
OpenAlexW2143124340

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.