Evidence map›Paper›PMID 24862737›Full record

ArticleJournal of experimental zoology. Part A, Ecological genetics and physiology2014

G-protein coupled estrogen receptor, estrogen receptor α, and progesterone receptor immunohistochemistry in the hypothalamus of aging female rhesus macaques given long-term estradiol treatment.

Michelle M Naugle, Long T Nguyen, Tyler K Merceron, Edward Filardo, William G M Janssen, John H Morrison, Peter R Rapp, Andrea C Gore

Open access · greenAbstract read
In one paragraph

Article in Journal of experimental zoology. Part A, Ecological genetics and physiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.3field-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

17 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. GPER-novel membrane oestrogen receptor.Clinical science (London, England : 1979) · 2016
    Review
  11. Article
  12. Review
  13. Perimenopause as a neurological transition state.Nature reviews. Endocrinology · 2015
    Review
  14. Article
  15. Expression of estrogen receptor α in the mouse cerebral cortex.Molecular and cellular endocrinology · 2015
    Article
  16. Article
  17. 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 4 institutions in 1 country.

Michelle M NaugleInstitute for Neuroscience, University of Texas at Austin, Austin, Texas.
Long T Nguyen
Tyler K Merceron
Edward Filardo
William G M Janssen
John H Morrison
Peter R Rapp
Andrea C Gore
The University of Texas at Austin · USAllen Institute for Brain Science · USBrown University · USNational Institute on Aging · US

Funding

The Nonhuman Primate CoreP01AG016765 · NIA · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI MORRISON, JOHN H. · 1999 to 2016
$26.1M
Primate Models of Neurocognitive Aging ZIAAG000352 · NIA · NATIONAL INSTITUTE ON AGING · PI RAPP, PETER R · 2009 to 2025
$20.8M
Estrogen and the Aging Primate BrainZIAAG000351 · NIA · NATIONAL INSTITUTE ON AGING · PI RAPP, PETER R · 2009 to 2019
$2.9M
NIA NIH HHS P01 AG016765NIA NIH HHS P01 AG16765
6 · The paper itself

Abstract

Steroid hormone receptors are widely and heterogeneously expressed in the brain, and are regulated by age and gonadal hormones. Our goal was to quantify effects of aging, long-term estradiol (E2 ) treatment, and their interactions, on expression of G protein-coupled estrogen receptor (GPER), estrogen receptor α (ERα) and progesterone receptor (PR) immunoreactivity in two hypothalamic regions, the arcuate (ARC) and the periventricular area (PERI) of rhesus monkeys as a model of menopause and hormone replacement. Ovariectomized (OVX) rhesus macaques were young (∼ 11 years) or aged (∼ 25 years), given oil (vehicle) or E2 every 3 weeks for 2 years. Immunohistochemistry and stereologic analysis of ERα, PR, and GPER was performed. More effects were detected for GPER than the other two receptors. Specifically, GPER cell density in the ARC and PERI, and the percent of GPER-immunoreactive cells in the PERI, were greater in aged than in young monkeys. In addition, we mapped the qualitative distribution of GPER in the monkey hypothalamus and nearby regions. For ERα, E2 treated monkeys tended to have higher cell density than vehicle monkeys in the ARC. The percent of PR density in the PERI tended to be higher in E2 than vehicle monkeys of both ages. This study shows that the aged hypothalamus maintains expression of hormone receptors with age, and that long-term cyclic E2 treatment has few effects on their expression, although GPER was affected more than ERα or PR. This result is surprising in light of evidence for E2 regulation of the receptors studied here, and differences may be due to the selected regions, long-term nature of E2 treatment, among other possibilities.

Indexed as

Macaca mulattaAgingAnimalsDrug Administration ScheduleEstradiolEstrogen Receptor alphaEstrogensFemaleImmunohistochemistryReceptors, G-Protein-CoupledReceptors, ProgesteroneEstradiolEstrogen Receptor alphaEstrogensReceptors, G-Protein-CoupledReceptors, Progesterone

Identifiers

PMID24862737
PMCPMC4282650
OpenAlexW1894051962

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.