Evidence map›Paper›PMID 23970786›Full record

ArticleEndocrinology2013

ERβ selective agonist inhibits angiotensin-induced cardiovascular pathology in female mice.

Ali Pedram, Mahnaz Razandi, Kenneth S Korach, Ramesh Narayanan, James T Dalton, Ellis R Levin

Open access · bronzeAbstract read
In one paragraph

Article in Endocrinology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

14 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Computational models of cardiac hypertrophy.Progress in biophysics and molecular biology · 2021
    Review
  5. Connecting sex differences, estrogen signaling, and microRNAs in cardiac fibrosis.Journal of molecular medicine (Berlin, Germany) · 2019
    Review
  6. Female Heart Health: Is GPER the Missing Link?Frontiers in endocrinology · 2019
    Review
  7. Article
  8. The Association of Estrogen Receptor-β Gene Variation With Salt-Sensitive Blood Pressure.The Journal of clinical endocrinology and metabolism · 2017
    Article
  9. Article
  10. Pharmacologic activation of estrogen receptor β increases mitochondrial function, energy expenditure, and brown adipose tissue.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2017
    Article
  11. Article
  12. Extranuclear estrogen receptor's roles in physiology: lessons from mouse models.American journal of physiology. Endocrinology and metabolism · 2014
    Article
  13. Review
  14. 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

6 authors at 3 institutions in 1 country.

Ali PedramMD, Medical Service (111-I), Long Beach Veterans Affairs Medical Center, 5901 East Seventh Street, Long Beach, California 90822. ellis.levin@va.gov.
Mahnaz Razandi
Kenneth S Korach
Ramesh Narayanan
James T Dalton
Ellis R Levin
Long Beach Medical Center · USNational Institute of Environmental Health Sciences · USUniversity of California, Irvine · US

Funding

Univ.of Calif., Irvine Cancer Center Support GrantP30CA062203 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI Joel E Milam · 1994 to 2026
$57.9M
Chemical Receptor Interactions In Reproduction And Hormonal ToxicityZIAES070065 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI KORACH, KENNETH S · 2009 to 2019
$29.6M
NCI NIH HHS CA-10036NCI NIH HHS P30 CA062203
6 · The paper itself

Abstract

Cardiac hypertrophy in humans can progress to cardiac failure if the underlying impetus is poorly controlled. An important direct stimulator of hypertrophy and its progression is the angiotensin II (AngII) peptide. AngII also causes hypertension that indirectly contributes to cardiac hypertrophy. Others and we have shown that estrogens acting through the estrogen receptor (ER)-β can inhibit AngII-induced or other forms of cardiac hypertrophy in mice. However, the proliferative effects of estrogen in breast and uterus that promote the development of malignancy preclude using the steroid to prevent cardiac disease progression. We therefore tested whether an ERβ selective agonist, β-LGND2, can prevent hypertension and cardiac pathology in female mice. AngII infusion over 3 weeks significantly stimulated systolic and diastolic hypertension, cardiac hypertrophy, and cardiac fibrosis, all significantly prevented by β-LGND2 in wild-type but not in ERβ genetically deleted mice. AngII stimulated the Akt kinase to phosphorylate and inhibit the glycogen synthase kinase-3β kinase, leading to GATA4 transcription factor activation and hypertrophic mRNA expression. As a novel mechanism, all these actions were opposed by estradiol and β-LGND2. Our findings provide additional understanding of the antihypertrophic effects of ERβ and serve as an impetus to test specific receptor agonists in humans to prevent the worsening of cardiovascular disease.

Indexed as

AngiotensinsAnimalsCardiomegalyEstradiolEstrogen Receptor betaFemaleHeartIsoquinolinesMiceMyocardiumOvariectomyRNA, MessengerSignal TransductionAngiotensinsbeta-LGND2EstradiolEstrogen Receptor betaIsoquinolinesRNA, Messenger

Identifiers

PMID23970786
PMCPMC5398592
OpenAlexW2162502779

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.