Evidence map›Paper›PMID 22427519›Full record

ArticleAmerican journal of physiology. Heart and circulatory physiology2012

Attenuation by sphingosine-1-phosphate of rat microvessel acute permeability response to bradykinin is rapidly reversible.

R H Adamson, R K Sarai, J F Clark, A Altangerel, T L Thirkill, F E Curry

Abstract read
In one paragraph

Article in American journal of physiology. Heart and circulatory physiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

15 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Acute alcohol intoxication-induced microvascular leakage.Alcoholism, clinical and experimental research · 2014
    Article
  10. Mechanosensing at the vascular interface.Annual review of biomedical engineering · 2014
    Review
  11. Article
  12. Article
  13. Microvascular permeability to water is independent of shear stress, but dependent on flow direction.American journal of physiology. Heart and circulatory physiology · 2013
    Article
  14. Tonic regulation of vascular permeability.Acta physiologica (Oxford, England) · 2013
    Review
  15. 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

6 authors at 1 institution in 1 country.

R H AdamsonDepartment of Physiology and Membrane Biology, School of Medicine, University of California at Davis, Davis, CA 95616, USA. rhadamson@ucdavis.edu
R K Sarai
J F Clark
A Altangerel
T L Thirkill
F E Curry
University of California, Davis · US

Funding

NEW APPROACH TO ENDOTHELIAL CLEFT STRUCTURER01HL044485 · NHLBI · UNIVERSITY OF CALIFORNIA DAVIS · PI CURRY, FITZ-ROY E · 1991 to 2010
$4.0M
WATER AND SOLUTE TRANSPORT ACROSS CAPILLARY ENDOTHELIUMR01HL028607 · NHLBI · UNIVERSITY OF CALIFORNIA DAVIS · PI CURRY, FITZ-ROY E · 1985 to 2014
$3.9M
TRANSPORT ACROSS CAPILLARY ENDOTHELIUMR37HL028607 · NHLBI · UNIVERSITY OF CALIFORNIA DAVIS · PI CURRY, FITZ-ROY E · 1992 to 2001
$504k
NHLBI NIH HHS HL-28607NHLBI NIH HHS HL-44485NHLBI NIH HHS R01 HL028607
6 · The paper itself

Abstract

To evaluate the hypothesis that sphingosine-1-phosphate (S1P) and cAMP attenuate increased permeability of individually perfused mesenteric microvessels through a common Rac1-dependent pathway, we measured the attenuation of the peak hydraulic conductivity (L(p)) in response to the inflammatory agent bradykinin (BK) by either S1P or cAMP. We varied the extent of exposure to each agent (test) and measured the ratio L(p)(test)/L(p)(BK alone) for each vessel (anesthetized rats). S1P (1 μM) added at the same time as BK (concurrent, no pretreatment) was as effective to attenuate the response to BK (L(p) ratio: 0.14 ± 0.05; n = 5) as concurrent plus pretreatment with S1P for 30 min (L(p) ratio: 0.26 ± 0.06; n = 11). The same pretreatment with S1P, but with no concurrent S1P, caused no inhibition of the BK response (L(p) ratio 1.07 ± 0.11; n = 8). The rapid on and off action of S1P demonstrated by these results was in contrast to cAMP-dependent changes induced by rolipram and forskolin (RF), which developed more slowly, lasted longer, and resulted in partial inhibition when given either as pretreatment or concurrent with BK. In cultured endothelium, there was no Rac activation or peripheral cortactin localization at 1 min with RF, but cortactin localization and Rac activation were maximal at 1 min with S1P. When S1P was removed, Rac activation returned to control within 2 min. Because of such differing time courses, S1P and cAMP are unlikely to act through fully common effector mechanisms.

Indexed as

AnimalsBradykininCapillary PermeabilityColforsinCyclic AMPLysophospholipidsMaleMicrovesselsModels, Animalrac1 GTP-Binding ProteinRatsRolipramSignal TransductionSphingosineTime FactorsVasodilator AgentsBradykininColforsinCyclic AMPLysophospholipidsrac1 GTP-Binding ProteinRac1 protein, ratRolipramSphingosinesphingosine 1-phosphateVasodilator Agents

Identifiers

PMID22427519
PMCPMC3362105
OpenAlexW1991636499

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.