Evidence map›Paper›PMID 31585360›Full record

ArticleNeurobiology of aging2019

Estradiol treatment improves biological rhythms in a preclinical rat model of menopause.

Weiling Yin, Jeremy C Borniger, Xutong Wang, Sean M Maguire, Mercedes L Munselle, Kelsey S Bezner, Haben M Tesfamariam, Alexandra N Garcia, Hans A Hofmann, Randy J Nelson and 1 more

Open access · greenAbstract read
In one paragraph

Article in Neurobiology of aging, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 34% 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

6 citing papers in PubMed, 14 citations in OpenAlex.

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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

11 authors at 3 institutions in 1 country.

Weiling YinDivision of Pharmacology and Toxicology, The University of Texas at Austin, Austin, TX, USA.
Jeremy C BornigerDepartment of Psychiatry & Behavioral Sciences, Stanford University School of Medicine, Stanford, CA, USA.
Xutong WangDivision of Pharmacology and Toxicology, The University of Texas at Austin, Austin, TX, USA; Department of Integrative Biology, The University of Texas at Austin, Austin, TX, USA.
Sean M MaguireDepartment of Integrative Biology, The University of Texas at Austin, Austin, TX, USA.
Mercedes L MunselleDivision of Pharmacology and Toxicology, The University of Texas at Austin, Austin, TX, USA.
Kelsey S BeznerDivision of Pharmacology and Toxicology, The University of Texas at Austin, Austin, TX, USA.
Haben M TesfamariamDivision of Pharmacology and Toxicology, The University of Texas at Austin, Austin, TX, USA.
Alexandra N GarciaPsychology Department, The University of Texas at Austin, Austin, TX, USA.
Hans A HofmannDepartment of Integrative Biology, The University of Texas at Austin, Austin, TX, USA; Institute for Neuroscience, The University of Texas at Austin, Austin, TX, USA.
Randy J NelsonDepartment of Neuroscience, Rockefeller Neuroscience Institute, West Virginia University, Morgantown, WV, USA.
Andrea C GoreDivision of Pharmacology and Toxicology, The University of Texas at Austin, Austin, TX, USA; Psychology Department, The University of Texas at Austin, Austin, TX, USA; Institute for Neuroscience, The University of Texas at Austin, Austin, TX, USA. Electronic address: andrea.gore@austin.utexas.edu.
The University of Texas at Austin · USStanford University · USWest Virginia University · US

Funding

The Nonhuman Primate CoreP01AG016765 · NIA · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI BAXTER, MARK G · 1999 to 2016
$26.1M
NIA NIH HHS P01 AG016765
6 · The paper itself

Abstract

The perimenopausal transition at middle age is often associated with hot flashes and sleep disruptions, metabolic changes, and other symptoms. Whereas the mechanisms for these processes are incompletely understood, both aging (AG) and a loss of ovarian estrogens play contributing roles. Furthermore, the timing of when estradiol (E) treatment should commence and for how long are key clinical questions in the management of symptoms. Using a rat model of surgical menopause, we determined the effects of regimens of E treatment with differing time at onset and duration of treatment on diurnal rhythms of activity and core temperature and on food intake and body weight. Reproductively mature (MAT, ∼4 months) or AG (∼11 months) female rats were ovariectomized, implanted intraperitoneally with a telemetry device, and given either a vehicle (V) or E subcutaneous capsule implantation. Rats were remotely recorded for 10 days per month for 3 (MAT) or 6 (AG) months. To ascertain whether delayed onset of treatment affected rhythms, a subset of AG-V rats had their capsules switched to E at the end of 3 months. Another set of AG-E rats had their capsules removed at 3 months to determine whether beneficial effects of E would persist. Overall, activity and temperature mesor, robustness, and amplitude declined with AG. Compared to V treatment, E-treated rats showed (1) better maintenance of body weight and food intake; (2) higher, more consolidated activity and temperature rhythms; and (3) higher activity and temperature robustness and amplitude. In the AG arm of the study, switching treatment from V to E or E to V quickly reversed these patterns. Thus, the presence of E was the dominant factor in determining stability and amplitude of locomotor activity and temperature rhythms. As a whole, the results show benefits of E treatment, even with a delay, on biological rhythms and physiological functions.

Indexed as

AnimalsBody TemperatureBody WeightCircadian RhythmEstradiolEstrogensFemaleMenopauseModels, AnimalMotor ActivityRats, Sprague-DawleyEstradiolEstrogensBody temperatureCircadian rhythmEstradiolHormone replacementHypothalamusMenopause

Identifiers

PMID31585360
PMCPMC6858967
OpenAlexW2972719852

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.