Evidence map›Paper›PMID 28478264›Full record

ArticleLife sciences2017

Vascular dysfunction and fibrosis in stroke-prone spontaneously hypertensive rats: The aldosterone-mineralocorticoid receptor-Nox1 axis.

Adam P Harvey, Augusto C Montezano, Katie Y Hood, Rheure A Lopes, Francisco Rios, Graziela Ceravolo, Delyth Graham, Rhian M Touyz

Open access · hybridAbstract read
In one paragraph

Article in Life sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

31 citing papers in PubMed, 52 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Vascular Aging and Central Aortic Blood Pressure: From Pathophysiology to Treatment.High blood pressure & cardiovascular prevention : the official journal of the Italian Society of Hypertension · 2020
    Review
  17. Oxidative Stress: A Unifying Paradigm in Hypertension.The Canadian journal of cardiology · 2020
    Review
  18. Article
  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

8 authors at 2 institutions in 2 countries.

Adam P HarveyInstitute of Cardiovascular and Medical Sciences, University of Glasgow, United Kingdom.
Augusto C MontezanoInstitute of Cardiovascular and Medical Sciences, University of Glasgow, United Kingdom.
Katie Y HoodInstitute of Cardiovascular and Medical Sciences, University of Glasgow, United Kingdom.
Rheure A LopesInstitute of Cardiovascular and Medical Sciences, University of Glasgow, United Kingdom.
Francisco RiosInstitute of Cardiovascular and Medical Sciences, University of Glasgow, United Kingdom.
Graziela CeravoloDepartment of Physiological Sciences, State University of Londrina, Londrina, Brazil.
Delyth GrahamInstitute of Cardiovascular and Medical Sciences, University of Glasgow, United Kingdom.
Rhian M TouyzInstitute of Cardiovascular and Medical Sciences, University of Glasgow, United Kingdom. Electronic address: Rhian.Touyz@glasgow.ac.uk.
University of Glasgow · GBUniversidade Estadual de Londrina · BR

Funding

British Heart Foundation CH/12/4/29762British Heart Foundation RE/13/5/30177British Heart Foundation RG/13/7/30099
6 · The paper itself

Abstract

aimsWe questioned whether aldosterone and oxidative stress play a role in vascular damage in severe hypertension and investigated the role of Nox1 in this process. MATERIALS AND

methodsWe studied mesenteric arteries, aortas and vascular smooth muscle cells (VSMC) from WKY and SHRSP rats. Vascular effects of eplerenone or canrenoic acid (CA) (mineralocorticoid receptor (MR) blockers), ML171 (Nox1 inhibitor) and EHT1864 (Rac1/2 inhibitor) were assessed. Nox1-knockout mice were also studied. Vessels and VSMCs were probed for Noxs, reactive oxygen species (ROS) and pro-fibrotic/inflammatory signaling. KEY

findingsBlood pressure and plasma levels of aldosterone and galectin-3 were increased in SHRSP versus WKY. Acetylcholine-induced vasorelaxation was decreased (61% vs 115%) and phenylephrine-induced contraction increased in SHRSP versus WKY (E SIGNIFICANCE: Our findings suggest that aldosterone, which is increased in SHRSP, induces vascular damage through MR-Nox1-p66Shc-mediated processes that modulate pro-fibrotic and pro-inflammatory signaling pathways.

Indexed as

Oxidative StressAcetylcholineAldosteroneAnimalsAortaBlood PressureGalectin 3HypertensionMaleMesenteric ArteriesMiceMice, KnockoutMuscle, Smooth, VascularNADH, NADPH OxidoreductasesNADPH Oxidase 1RatsAcetylcholineAldosteroneGalectin 3NADH, NADPH OxidoreductasesNADPH Oxidase 1NOX1 protein, mouseNOX1 protein, ratReactive Oxygen SpeciesReceptors, MineralocorticoidHypertensionMineralocorticoid receptorsOxidative stressSignal transductionVascular functionVascular remodeling

Identifiers

PMID28478264
PMCPMC5446265
OpenAlexW2610459919

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.