Evidence map›Paper›PMID 28680060›Full record

ArticleScientific reports2017

Novel oestrogen receptor β-selective ligand reduces obesity and depressive-like behaviour in ovariectomized mice.

Daimei Sasayama, Nobuhiro Sugiyama, Shigeru Yonekubo, Akiko Pawlak, Hiroyasu Murasawa, Mie Nakamura, Morimichi Hayashi, Takashi Ogawa, Makoto Moro, Shinsuke Washizuka and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.5field-weighted citation impact, top 15% 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

16 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Ovarian status modulates endocrine and neuroinflammatory responses to a murine mammary tumor.American journal of physiology. Regulatory, integrative and comparative physiology · 2022
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  14. Sex ModulatesFrontiers in microbiology · 2018
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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

13 authors at 2 institutions in 1 country.

Daimei SasayamaDepartment of Psychiatry, Shinshu University School of Medicine, Matsumoto, Nagano, 390-8621, Japan.
Nobuhiro SugiyamaDepartment of Psychiatry, Shinshu University School of Medicine, Matsumoto, Nagano, 390-8621, Japan. nsugi@shinshu-u.ac.jp.
Shigeru YonekuboDiscovery Research I, R&D, Kissei Pharmaceutical Co., Ltd., 4365-1 Kashiwabara, Hotaka, Azumino, Nagano, 399-8304, Japan.
Akiko PawlakNihon Bioresearch Inc. 6-104, Majima, Fukuju-cho, Hashima, Gifu, 501-6251, Japan.
Hiroyasu MurasawaNihon Bioresearch Inc. 6-104, Majima, Fukuju-cho, Hashima, Gifu, 501-6251, Japan.
Mie NakamuraNihon Bioresearch Inc. 6-104, Majima, Fukuju-cho, Hashima, Gifu, 501-6251, Japan.
Morimichi HayashiSafety Research Laboratory, R&D, Kissei Pharmaceutical Co., Ltd., 2320-1 Maki, Azumino, Nagano, 399-8304, Japan.
Takashi OgawaSafety Research Laboratory, R&D, Kissei Pharmaceutical Co., Ltd., 2320-1 Maki, Azumino, Nagano, 399-8304, Japan.
Makoto MoroBiologics Research, R&D, Kissei Pharmaceutical Co., Ltd., 4365-1 Kashiwabara, Hotaka, Azumino, Nagano, 399-8304, Japan.
Shinsuke WashizukaDepartment of Psychiatry, Shinshu University School of Medicine, Matsumoto, Nagano, 390-8621, Japan.
Naoji AmanoDepartment of Drug Discovery Science, Shinshu University School of Medicine, Matsumoto, Nagano, 390-8621, Japan.
Kazuhiro HongoDepartment of Drug Discovery Science, Shinshu University School of Medicine, Matsumoto, Nagano, 390-8621, Japan.
Hideki OhnotaDepartment of Drug Discovery Science, Shinshu University School of Medicine, Matsumoto, Nagano, 390-8621, Japan.
Shinshu University · JPKissei Pharmaceutical (Japan) · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hormonal changes due to menopause can cause various health problems including weight gain and depressive symptoms. Multiple lines of evidence indicate that oestrogen receptors (ERs) play a major role in postmenopausal obesity and depression. However, little is known regarding the ER subtype-specific effects on obesity and depressive symptoms. To delineate potential effects of ERβ activation in postmenopausal women, we investigated the effects of a novel oestrogen receptor β-selective ligand (C-1) in ovariectomized mice. Uterine weight, depressive behaviour, and weight gain were examined in sham-operated control mice and ovariectomized mice administered placebo, C-1, or 17β-oestradiol (E2). Administration of C-1 or E2 reduced body weight gain and depressive-like behaviour in ovariectomized mice, as assessed by the forced swim test. In addition, administration of E2 to ovariectomized mice increased uterine weight, but administration of C-1 did not result in a significant increase in uterine weight. These results suggest that the selective activation of ERβ in ovariectomized mice may have protective effects against obesity and depressive-like behaviour without causing an increase in uterine weight. The present findings raise the possibility of the application of ERβ-ligands such as C-1 as a novel treatment for obesity and depression in postmenopausal women.

Indexed as

AnimalsDepressionDisease Models, AnimalEstradiolEstrogen Receptor betaFemaleLigandsMiceMolecular StructureObesityOrgan SizeOvariectomyPostmenopauseSelective Estrogen Receptor ModulatorsUterusWeight GainEstradiolEstrogen Receptor betaLigandsSelective Estrogen Receptor Modulators

Identifiers

PMID28680060
PMCPMC5498485
OpenAlexW2727813186

What OpenQuestion holds

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LicenceCC BY
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.