Evidence map›Paper›PMID 26367262›Full record

ArticlePloS one2015

Sphingosine-1-Phosphate Signaling Regulates Myogenic Responsiveness in Human Resistance Arteries.

Sonya Hui, Andrew S Levy, Daniel L Slack, Marcus J Burnstein, Lee Errett, Daniel Bonneau, David Latter, Ori D Rotstein, Steffen-Sebastian Bolz, Darcy Lidington and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

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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

11 authors at 2 institutions in 1 country.

Sonya HuiToronto Centre for Microvascular Medicine, University of Toronto and St. Michael's Hospital, Toronto, Canada; Keenan Research Centre for Biomedical Science, St. Michael's Hospital, Toronto, Canada; Department of Physiology, University of Toronto, Toronto, Canada.
Andrew S LevyToronto Centre for Microvascular Medicine, University of Toronto and St. Michael's Hospital, Toronto, Canada; Keenan Research Centre for Biomedical Science, St. Michael's Hospital, Toronto, Canada; Department of Physiology, University of Toronto, Toronto, Canada.
Daniel L SlackDepartment of Physiology, University of Toronto, Toronto, Canada.
Marcus J BurnsteinKeenan Research Centre for Biomedical Science, St. Michael's Hospital, Toronto, Canada; Department of Surgery, St. Michael's Hospital and University of Toronto, Toronto, Canada.
Lee ErrettKeenan Research Centre for Biomedical Science, St. Michael's Hospital, Toronto, Canada; Department of Surgery, St. Michael's Hospital and University of Toronto, Toronto, Canada.
Daniel BonneauKeenan Research Centre for Biomedical Science, St. Michael's Hospital, Toronto, Canada; Department of Surgery, St. Michael's Hospital and University of Toronto, Toronto, Canada.
David LatterKeenan Research Centre for Biomedical Science, St. Michael's Hospital, Toronto, Canada; Department of Surgery, St. Michael's Hospital and University of Toronto, Toronto, Canada.
Ori D RotsteinKeenan Research Centre for Biomedical Science, St. Michael's Hospital, Toronto, Canada; Department of Surgery, St. Michael's Hospital and University of Toronto, Toronto, Canada.
Steffen-Sebastian BolzToronto Centre for Microvascular Medicine, University of Toronto and St. Michael's Hospital, Toronto, Canada; Keenan Research Centre for Biomedical Science, St. Michael's Hospital, Toronto, Canada; Department of Physiology, University of Toronto, Toronto, Canada; Heart & Stroke / Richard Lewar Centre of Excellence in Cardiovascular Research, University of Toronto, Toronto, Canada.
Darcy LidingtonToronto Centre for Microvascular Medicine, University of Toronto and St. Michael's Hospital, Toronto, Canada; Keenan Research Centre for Biomedical Science, St. Michael's Hospital, Toronto, Canada; Department of Physiology, University of Toronto, Toronto, Canada.
Julia Voigtlaender-BolzToronto Centre for Microvascular Medicine, University of Toronto and St. Michael's Hospital, Toronto, Canada; Keenan Research Centre for Biomedical Science, St. Michael's Hospital, Toronto, Canada; Department of Physiology, University of Toronto, Toronto, Canada; Department of Anaesthesia, St. Michael's Hospital and University of Toronto, Toronto, Canada.
St. Michael's Hospital · CAUniversity of Toronto · CA

Funding

Canadian Institutes of Health Research FRN-119345Canadian Institutes of Health Research FRN-37779
6 · The paper itself

Abstract

We recently identified sphingosine-1-phosphate (S1P) signaling and the cystic fibrosis transmembrane conductance regulator (CFTR) as prominent regulators of myogenic responsiveness in rodent resistance arteries. However, since rodent models frequently exhibit limitations with respect to human applicability, translation is necessary to validate the relevance of this signaling network for clinical application. We therefore investigated the significance of these regulatory elements in human mesenteric and skeletal muscle resistance arteries. Mesenteric and skeletal muscle resistance arteries were isolated from patient tissue specimens collected during colonic or cardiac bypass surgery. Pressure myography assessments confirmed endothelial integrity, as well as stable phenylephrine and myogenic responses. Both human mesenteric and skeletal muscle resistance arteries (i) express critical S1P signaling elements, (ii) constrict in response to S1P and (iii) lose myogenic responsiveness following S1P receptor antagonism (JTE013). However, while human mesenteric arteries express CFTR, human skeletal muscle resistance arteries do not express detectable levels of CFTR protein. Consequently, modulating CFTR activity enhances myogenic responsiveness only in human mesenteric resistance arteries. We conclude that human mesenteric and skeletal muscle resistance arteries are a reliable and consistent model for translational studies. We demonstrate that the core elements of an S1P-dependent signaling network translate to human mesenteric resistance arteries. Clear species and vascular bed variations are evident, reinforcing the critical need for further translational study.

Indexed as

AdolescentAdultAnimalsCystic Fibrosis Transmembrane Conductance RegulatorFemaleHumansMaleMesenteric ArteriesMiceMuscle ContractionMuscle, Smooth, VascularPyrazolesPyridinesReceptors, LysosphingolipidSignal TransductionSphingosineCFTR protein, humanCystic Fibrosis Transmembrane Conductance RegulatorJTE 013PyrazolesPyridinesReceptors, Lysosphingolipidsphingenine-1-phosphateSphingosine

Identifiers

PMID26367262
PMCPMC4569583
OpenAlexW2190093070

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.