Evidence map›Paper›PMID 18787021›Full record

ArticleEndocrinology2009

Role of aging versus the loss of estrogens in the reduction in vascular function in female rats.

James P Stice, Jason P Eiserich, A A Knowlton

Open access · bronzeAbstract read
In one paragraph

Article in Endocrinology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

21 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Promoting healthy cardiovascular aging: emerging topics.The journal of cardiovascular aging · 2022
    Article
  3. Article
  4. Article
  5. Article
  6. Role of estrogen in diastolic dysfunction.American journal of physiology. Heart and circulatory physiology · 2014
    Review
  7. Article
  8. Review
  9. Article
  10. Influence of estradiol supplementation on neuropeptide Y neurotransmission in skeletal muscle arterioles of F344 rats.American journal of physiology. Regulatory, integrative and comparative physiology · 2012
    Article
  11. Article
  12. Estrogen and the cardiovascular system.Pharmacology & therapeutics · 2012
    Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Membrane-initiated actions of estrogen on the endothelium.Molecular and cellular endocrinology · 2009
    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

3 authors at 2 institutions in 1 country.

James P SticeMolecular and Cellular Cardiology, Cardiovascular Division, Department of Medicine, University of California, Davis, One Shields Avenue, Davis, California 95616, USA.
Jason P Eiserich
A A Knowlton
University of California, Davis · USVeterans Health Administration · US

Funding

AGING, ESTROGEN, HSPS AND MYOCARDIAL ISCHEMIAR01AG019327 · NIA · UNIVERSITY OF CALIFORNIA DAVIS · PI KNOWLTON, ANNE A · 2001 to 2005
$1.1M
Estrogen, Aging and Vascular InflammationI01BX000839 · VA · VA NORTHERN CALIFORNIA HEALTH CARE SYS · PI KNOWLTON, ANNE A · 2011 to 2014
–
BLRD VA I01 BX000839NIA NIH HHS AG19327NIA NIH HHS R01 AG019327
6 · The paper itself

Abstract

Although aging is known to lead to increased vascular stiffness, the role of estrogens in the prevention of age-related changes in the vasculature remains to be elucidated. To address this, we measured vascular function in the thoracic aorta in adult and old ovariectomized (ovx) rats with and without immediate 17beta-estradiol (E2) replacement. In addition, aortic mRNA and protein were analyzed for proteins known to be involved in vasorelaxation. Aging in combination with the loss of estrogens led to decreased vasorelaxation in response to acetylcholine and sodium nitroprusside, indicating either smooth muscle dysfunction and/or increased fibrosis. Loss of estrogens led to increased vascular tension in response to phenylephrine, which could be partially restored by E2 replacement. Levels of endothelial nitric oxide synthase and inducible nitric oxide synthase did not differ among the groups, nor did total nitrite plus nitrate levels. Old ovx exhibited decreased expression of both the alpha and beta-subunits of soluble guanylyl cyclase (sGC) and had impaired nitric oxide signaling in the vascular smooth muscle. Immediate E2 replacement in the aged ovx prevented both the impairment in vasorelaxation, and the decreased sGC receptor expression and abnormal sGC signaling within the vascular smooth muscle.

Indexed as

AgingAnimalsAortaBlood VesselsEstrogensFemaleIsometric ContractionMuscle, Smooth, VascularNitric OxideOvariectomyPolymerase Chain ReactionRatsRats, Inbred BNRNAVasoconstrictionVasodilationEstrogensNitric OxideRNA

Identifiers

PMID18787021
PMCPMC2630896
OpenAlexW2086715796

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.