Evidence map›Paper›PMID 31974436›Full record

ArticleScientific reports2020

Ovarian mitochondrial dynamics and cell fate regulation in an androgen-induced rat model of polycystic ovarian syndrome.

Reza Salehi, Hannah L Mazier, Anne-Laure Nivet, Arkadiy A Reunov, Patricia Lima, Qi Wang, Arianna Fiocco, Ciro Isidoro, Benjamin K Tsang

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
6.5field-weighted citation impact, top 3% 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

35 citing papers in PubMed, 61 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

9 authors at 3 institutions in 2 countries.

Reza SalehiChronic Disease Program, Ottawa Hospital Research Institute, Ottawa, Canada.
Hannah L MazierChronic Disease Program, Ottawa Hospital Research Institute, Ottawa, Canada.
Anne-Laure NivetChronic Disease Program, Ottawa Hospital Research Institute, Ottawa, Canada.
Arkadiy A ReunovElectron Microscopy Laboratory, University of Ottawa Heart Institute, Ottawa, Canada.
Patricia LimaChronic Disease Program, Ottawa Hospital Research Institute, Ottawa, Canada.
Qi WangChronic Disease Program, Ottawa Hospital Research Institute, Ottawa, Canada.
Arianna FioccoDepartment of Cellular & Molecular Medicine and Obstetrics & Gynecology, University of Ottawa, Ottawa, Canada.
Ciro IsidoroLaboratory of Molecular Pathology, Department of Health Sciences, Università del Piemonte Orientale "A. Avogadro", Via P. Solaroli 17, 28100, Novara, Italy. ciro.isidoro@med.uniupo.it.ORCID http://orcid.org/0000-0002-5494-3034
Benjamin K TsangChronic Disease Program, Ottawa Hospital Research Institute, Ottawa, Canada. btsang@ohri.ca.
University of Ottawa · CAOttawa Hospital · CAUniversità degli Studi del Piemonte Orientale “Amedeo Avogadro” · IT

Funding

Gouvernement du Canada | Canadian Institutes of Health Research (Instituts de Recherche en Santé du Canada) MOP-119381
6 · The paper itself

Abstract

In this study, we investigated in an androgenized rat model the involvement of autophagy and mitochondrial dynamics in granulosa cells in the pathogenesis of polycystic ovarian syndrome (PCOS) and its modulation by exogenous gonadotropin (eCG). We found 5α-dihydrotestosterone (DHT) treatment reduces ovarian length and weight with predominantly late antral and/or preovulatory stage follicles and no corpora lutea. DHT increased the population of large lysosomes (>50 micron) and macroautophagy, an event associated with granulosa cell apoptosis. Increased granulosa cell Dynamin Related Protein 1 (Drp1) content in the DHT group was accompanied by increased circular and constricted, but reduced rod-shaped, mitochondria. eCG eliminated all atypical follicles and increased the number of late antral and preovulatory follicles with less granulosa cell apoptosis. eCG-treated rats had a higher proportion of connected mitochondria, and in combination with DHT had a lower proportion of circular and constricted mitochondria than rats treated with DHT alone, suggesting that eCG induces mitochondrial fusion and attenuates fission in granulosa cells. In summary, we observed that DHT-induced up-regulation of Drp1 is associated with excessive mitochondrial fission, macroautophagy and apoptosis in granulosa cells at the antral stage of development in an androgenized rat model for PCOS, a response partially attenuated by exogenous gonadotropin.

Indexed as

AndrogensAnimalsApoptosisAutophagyDihydrotestosteroneDisease Models, AnimalDynaminsFemaleGonadotropinsGranulosa CellsMitochondriaMitochondrial DynamicsPolycystic Ovary SyndromeRatsRats, Sprague-DawleyAndrogensDihydrotestosteroneDnm1l protein, mouseDynaminsGonadotropins

Identifiers

PMID31974436
PMCPMC6978404
OpenAlexW3000979264

What OpenQuestion holds

Textmetadata
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.