Evidence map›Paper›PMID 35881588›Full record

ArticlePloS one2022

Short chain fatty acid, acetate restores ovarian function in experimentally induced PCOS rat model.

Kehinde S Olaniyi, Al-Amin M Bashir, Stephanie E Areloegbe, Isaiah W Sabinari, Christopher O Akintayo, Adesola A Oniyide, Ayodeji Aturamu

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
7.4field-weighted citation impact, top 2% 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

25 citing papers in PubMed, 40 citations in OpenAlex.

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  19. Fecal propionate is a signature of insulin resistance in polycystic ovary syndrome.Frontiers in cellular and infection microbiology · 2024
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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

7 authors at 2 institutions in 1 country.

Kehinde S OlaniyiDepartment of Physiology, Cardio/Repro-metabolic and Microbiome Research Unit, College of Medicine and Health Sciences, Afe Babalola University, Ado-Ekiti, Nigeria.ORCID 0000-0002-8229-9688
Al-Amin M BashirDepartment of Physiology, Cardio/Repro-metabolic and Microbiome Research Unit, College of Medicine and Health Sciences, Afe Babalola University, Ado-Ekiti, Nigeria.
Stephanie E AreloegbeDepartment of Physiology, Cardio/Repro-metabolic and Microbiome Research Unit, College of Medicine and Health Sciences, Afe Babalola University, Ado-Ekiti, Nigeria.
Isaiah W SabinariHOPE Cardiometabolic Research Team & Department of Physiology, College of Health Sciences, University of Ilorin, Ilorin, Nigeria.
Christopher O AkintayoDepartment of Physiology, Cardio/Repro-metabolic and Microbiome Research Unit, College of Medicine and Health Sciences, Afe Babalola University, Ado-Ekiti, Nigeria.
Adesola A OniyideDepartment of Physiology, Cardio/Repro-metabolic and Microbiome Research Unit, College of Medicine and Health Sciences, Afe Babalola University, Ado-Ekiti, Nigeria.
Ayodeji AturamuDepartment of Physiology, Cardio/Repro-metabolic and Microbiome Research Unit, College of Medicine and Health Sciences, Afe Babalola University, Ado-Ekiti, Nigeria.
Afe Babalola University · NGUniversity of Ilorin · NG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPolycystic ovarian syndrome (PCOS) is pathogenically characterized with hyperandrogenism and metabolic alterations, which often result in ovarian changes and infertility in women of reproductive age. Epigenetic changes have been linked to the development of PCOS. However, the involvement of epigenetic regulator, histone deacetylase (HDAC) in PCOS-driven ovarian dysfunction is not clear. Howbeit, the present study hypothesized that acetate, an HDAC inhibitor (HDACi) would protect against ovarian dysfunction in experimentally induced PCOS. MATERIALS AND

methodsFemale Wistar rats weighing 120-150 g were randomly divided into four groups (n = 6). The groups received vehicle, sodium acetate (200 mg/kg), letrozole (1 mg/kg) and letrozole with acetate by oral gavage respectively. The administrations were done daily for 21 days.

resultsThe rat model of PCOS had increased body weight and ovarian weight, 1-hr postload glucose and plasma insulin, testosterone and LH/FSH ratio as well as reduced insulin sensitivity and plasma 17-β estradiol and sex hormone binding globulin. This model of PCOS in addition showed a significant increase in plasma and ovarian triglyceride, total cholesterol, TNF-α and HDAC, and ovarian malondialdehyde as well as a significant reduction in ovarian glutathione peroxidase/reduced glutathione and NrF2 with the histology of ovarian tissues showing disrupted morphology with significant increase in the number of degenerated follicles compared with control group. These alterations were however attenuated when treated with HDACi, acetate.

conclusionAltogether, the present results suggest that acetate protects ovarian function with evidence of normal growing follicles and enhanced circulating 17-β estradiol by inhibition of HDAC.

Indexed as

Polycystic Ovary SyndromeAcetatesAnimalsEstradiolFatty Acids, VolatileFemaleLetrozoleRatsRats, WistarAcetatesEstradiolFatty Acids, VolatileLetrozole

Identifiers

PMID35881588
PMCPMC9321379
OpenAlexW4288039938

What OpenQuestion holds

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LicenceCC BY
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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.