Evidence map›Paper›PMID 41758920›Full record

ArticleMolecular human reproduction2026

Butyric acid-based self-assembling nanoparticles: a potential strategy to prevent development of polycystic ovary syndrome.

Nanoka Sakaguchi, Akari Kusamoto, Miyuki Harada, Babita Shashni, Airi Komura, Ayaka Teshima, Tsurugi Tanaka, Hiroshi Koike, Zixin Xu, Yuma Kawahara and 8 more

Abstract read
In one paragraph

Article in Molecular human reproduction, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Review
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

18 authors.

Nanoka SakaguchiDepartment of Obstetrics and Gynecology, Faculty of Medicine, The University of Tokyo, Tokyo, Japan.ORCID 0009-0005-6917-5110
Akari KusamotoDepartment of Obstetrics and Gynecology, Faculty of Medicine, The University of Tokyo, Tokyo, Japan.
Miyuki HaradaDepartment of Obstetrics and Gynecology, Faculty of Medicine, The University of Tokyo, Tokyo, Japan.ORCID 0000-0003-1071-5600
Babita ShashniDepartment of Materials Science, Graduate School of Pure and Applied Sciences, University of Tsukuba, Ibaraki, Japan.
Airi KomuraDepartment of Obstetrics and Gynecology, Faculty of Medicine, The University of Tokyo, Tokyo, Japan.
Ayaka TeshimaDepartment of Obstetrics and Gynecology, Faculty of Medicine, The University of Tokyo, Tokyo, Japan.
Tsurugi TanakaDepartment of Obstetrics and Gynecology, Faculty of Medicine, The University of Tokyo, Tokyo, Japan.
Hiroshi KoikeDepartment of Obstetrics and Gynecology, Faculty of Medicine, The University of Tokyo, Tokyo, Japan.
Zixin XuDepartment of Obstetrics and Gynecology, Faculty of Medicine, The University of Tokyo, Tokyo, Japan.
Yuma KawaharaDepartment of Obstetrics and Gynecology, Faculty of Medicine, The University of Tokyo, Tokyo, Japan.
Chihiro TsuchidaDepartment of Obstetrics and Gynecology, Faculty of Medicine, The University of Tokyo, Tokyo, Japan.
Chisato KunitomiDepartment of Obstetrics and Gynecology, Faculty of Medicine, The University of Tokyo, Tokyo, Japan.
Nozomi TakahashiDepartment of Obstetrics and Gynecology, Faculty of Medicine, The University of Tokyo, Tokyo, Japan.
Yoko UrataDepartment of Obstetrics and Gynecology, Faculty of Medicine, The University of Tokyo, Tokyo, Japan.ORCID 0000-0001-5455-4509
Osamu Wada-HiraikeDepartment of Obstetrics and Gynecology, Faculty of Medicine, The University of Tokyo, Tokyo, Japan.
Yasushi HirotaDepartment of Obstetrics and Gynecology, Faculty of Medicine, The University of Tokyo, Tokyo, Japan.ORCID 0000-0003-0241-9780
Yukio NagasakiDepartment of Materials Science, Graduate School of Pure and Applied Sciences, University of Tsukuba, Ibaraki, Japan.
Yutaka OsugaDepartment of Obstetrics and Gynecology, Faculty of Medicine, The University of Tokyo, Tokyo, Japan.ORCID 0000-0002-6660-1066

Funding

Astellas Foundation for Research on Metabolic Disorders FY2023 ResearchJapan Society for the Promotion of Science (JSPS) 19H05458Japan Society for the Promotion of Science (JSPS) 21j12871Japan Society for the Promotion of Science (JSPS) 21k16808Japan Society for the Promotion of Science (JSPS) 22k09614Japan Society for the Promotion of Science (JSPS) 23k08816Japan Society for the Promotion of Science (JSPS) 23k15803Japan Society for the Promotion of Science (JSPS) 23k19667Japan Society for the Promotion of Science (JSPS) 24k23506Japan Society for the Promotion of Science (JSPS) 25k20080Kanzawa Medical Research Foundation Research Grant 2023
6 · The paper itself

Abstract

Polycystic ovary syndrome (PCOS) is the most common endocrine disorder affecting women of reproductive age and cannot currently be cured or prevented fundamentally. Prenatal androgen exposure is a key factor in PCOS development, and both PCOS patients and animal models exhibit gut microbiota alterations. We previously demonstrated that prenatally androgenized (PNA) model mice display changes of gut microbiota before the manifestation of PCOS phenotypes, suggesting that an intervention targeting gut microbiota from the early stage of life can prevent development of PCOS. Butyric acid, a short-chain fatty acid produced by bacteria in the intestines, has various physiological effects. We investigated whether butyric acid could prevent PCOS phenotypes in PNA mice when administered from the early stage of life as a nanoparticle-based donor. We have developed butyric acid-based self-assembling nanoparticles (BNP), which release butyric acid in a sustained manner when exposed to digestive enzymes so that butyrate is delivered to the intestines. Control and PNA offspring were administered water containing or lacking BNP from just after weaning until 20 weeks of age. Reproductive and metabolic phenotypes were compared among these offspring (n = 10-14 for each group). Administration of BNP normalized irregular estrus cyclicity and improved the polycystic ovarian morphology, as evidenced by smaller numbers of atretic follicles in PNA offspring. Regarding metabolic phenotypes, administration of BNP improved hypertrophy of adipocytes and insulin resistance. Furthermore, analysis of the gut microbiota suggested that these primary effects were caused by butyrate itself, with an increase in certain butyrate-producing bacteria supporting this mechanism. The present findings indicate that administration of butyric acid to PNA offspring, which are at high risk of developing PCOS, from the early stage of life effectively prevents development of PCOS phenotypes at reproductive ages. Further exploration is necessary to clarify the mechanism by which butyric acid prevents development of PCOS.

Indexed as

Butyric AcidNanoparticlesPolycystic Ovary SyndromeAndrogensAnimalsDisease Models, AnimalFemaleGastrointestinal MicrobiomeHumansMicePregnancyPrenatal Exposure Delayed EffectsAndrogensButyric Acidandrogenbutyric aciddysbiosisgastrointestinal microbiomenanoparticle-type butyric acid donorpolycystic ovary syndromeprenatal androgen exposureshort-chain fatty acid

Identifiers

PMID41758920
PMCPMC13016983

What Socratic holds

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LicenceCC BY-NC
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Registered trials

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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 Socratic graph.