Evidence map›Paper›PMID 21076298›Full record

ReviewCurrent opinion in nephrology and hypertension2011

New insights into angiotensin receptor actions: from blood pressure to aging.

Johannes Stegbauer, Thomas M Coffman

Abstract readReview
In one paragraph

Review in Current opinion in nephrology and hypertension, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
8.0field-weighted citation impact, top 2% 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

38 citing papers in PubMed, 104 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. The mechanisms of vascular aging.Aging medicine (Milton (N.S.W)) · 2021
    Review
  6. Kinins and Kinin Receptors in Cardiovascular and Renal Diseases.Pharmaceuticals (Basel, Switzerland) · 2021
    Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Pitavastatin Regulates Ang II Induced Proliferation and Migration via IGFBP-5 in VSMC.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2015
    Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Review
  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

2 authors at 2 institutions in 1 country.

Johannes StegbauerDivision of Nephrology, Department of Medicine, Duke University Medical Center, Durham, North Carolina 27710, USA.
Thomas M Coffman
Duke Medical Center · USDurham VA Medical Center · US

Funding

ANGIOTENSIN RECEPTOR GENES AND BLOOD PRESSURE REGULATIONR01HL056122 · NHLBI · DUKE UNIVERSITY · PI COFFMAN, THOMAS M · 1997 to 2010
$3.2M
NHLBI NIH HHS HL056122 13NHLBI NIH HHS R01 HL056122
6 · The paper itself

Abstract

purpose of reviewThe renin-angiotensin system (RAS) is critical for cardiovascular control, impacting normal physiology and disease pathogenesis. Although several biologically active peptides are generated by this system, its major actions are mediated by angiotensin II acting through its type 1 (AT1) and type 2 (AT2) receptors. Along with their effects to influence blood pressure and hemodynamics, recent studies have provided evidence that angiotensin receptors influence a range of processes independent from hemodynamic effects. RECENT

findingsThis review is focused on new molecular mechanisms underlying actions of AT1 receptors to influence vasoconstriction, inflammation, immune responses, and longevity. Moreover, we also highlight new advances in understanding functions of the AT2 receptor in end-organ damage, emphasizing the AT2 receptor as a potential therapeutic target in cardiovascular diseases. SUMMARY: Here we review recent advances in understanding the role of angiotensin receptors in normal physiology and disease states, focusing on their properties that may contribute to blood pressure regulation, end-organ damage, autoimmune disease and longevity.

Indexed as

AgingAnimalsAutoimmune DiseasesBlood PressureHomeostasisHumansReceptor, Angiotensin, Type 1Receptor, Angiotensin, Type 2Signal TransductionReceptor, Angiotensin, Type 1Receptor, Angiotensin, Type 2

Identifiers

PMID21076298
PMCPMC3087382
OpenAlexW2088501994

What OpenQuestion holds

Textmetadata
LicenceTDM
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.