Evidence map›Paper›PMID 15655500›Full record

ArticleBritish journal of pharmacology2005

Aldosterone does not mediate angiotensin II-induced atherosclerosis and abdominal aortic aneurysms.

Lisa A Cassis, Marc J Helton, Deborah A Howatt, Victoria L King, Alan Daugherty

Open access · bronzeAbstract read
In one paragraph

Article in British journal of pharmacology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

20 citing papers in PubMed, 48 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Mineralocorticoid receptor antagonism inhibits vein graft remodeling in mice.The Journal of thoracic and cardiovascular surgery · 2013
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Experimental models of abdominal aortic aneurysms.The open cardiovascular medicine journal · 2010
    Article
  12. Circulating neprilysin clears brain amyloid.Molecular and cellular neurosciences · 2010
    Article
  13. Article
  14. The role of aldosterone in mediating the dependence of angiotensin hypertension on IL-6.American journal of physiology. Regulatory, integrative and comparative physiology · 2009
    Article
  15. Expression of neprilysin in skeletal muscle reduces amyloid burden in a transgenic mouse model of Alzheimer disease.Molecular therapy : the journal of the American Society of Gene Therapy · 2009
    Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. Angiotensin II and abdominal aortic aneurysms.Current hypertension reports · 2004
    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

5 authors at 1 institution in 1 country.

Lisa A CassisGraduate Center for Nutritional Sciences, Charles T. Wethington Building, University of Kentucky, Lexington, KY 40536, U.S.A. lcassis@uky.edu
Marc J Helton
Deborah A Howatt
Victoria L King
Alan Daugherty
University of Kentucky · US

Funding

Sources and effects of angiotensin peptides in atherosclerosisR01HL062846 · NHLBI · UNIVERSITY OF KENTUCKY · PI DAUGHERTY, ALAN · 2000 to 2012
$2.8M
NHLBI NIH HHS HL 62846NHLBI NIH HHS R01 HL062846
6 · The paper itself

Abstract

We have demonstrated previously that infusion of angiotensin II (AngII) into hyperlipidemic mice augments atherosclerosis and results in the formation of abdominal aortic aneurysms (AAA). The purpose of this study was to determine the role of aldosterone in these AngII-induced vascular pathologies. Male apolipoprotein E-/- (apoE) mice were infused with either vehicle or aldosterone (50 or 200 ng kg(-1) min(-1)). Arterial blood pressure was determined throughout the study and serum lipid concentrations and vascular pathology were quantified after 28 days of infusion. Infusion of aldosterone did not influence body weight or serum cholesterol concentrations. Kidney weight was increased dose-dependently by aldosterone infusion. Systolic blood pressure was not significantly altered by aldosterone. Plasma aldosterone concentrations were increased dose-dependently by infusion of aldosterone. However, there was no effect of aldosterone on the extent of atherosclerosis and AAAs were not formed. Implantation of pellets containing spironolactone (16 mg kg(-1) day(-1)) in AngII-infused apoE-/- mice (1000 ng kg(-1) min(-1)) had no effect on AngII-induced elevations in blood pressure. Plasma aldosterone concentration was not influenced by coadministration of spironolactone with AngII. Spironolactone administration did not influence the extent of atherosclerosis. Moreover, spironolactone had no significant effect on AngII-induced AAA (incidence of AAA formation: 80 versus 70% for vehicle versus spironolactone, respectively; not significant). These studies demonstrate that the AngII-induced vascular pathologies of atherosclerosis and AAA formation are not mediated through aldosterone.

Indexed as

AldosteroneAngiotensin IIAnimalsAortic Aneurysm, AbdominalApolipoproteins EArteriosclerosisBlood PressureBody WeightCholesterolDiureticsDose-Response Relationship, DrugMaleMiceMice, Inbred C57BLMice, KnockoutMineralocorticoid Receptor AntagonistsAldosteroneAngiotensin IIApolipoproteins ECholesterolDiureticsMineralocorticoid Receptor AntagonistsSpironolactone

Identifiers

PMID15655500
PMCPMC1576022
OpenAlexW2036987285

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.