Evidence map›Paper›PMID 41428223›Full record

ArticleArchives of toxicology2026

Bisphenol Z at environmentally relevant dose dysregulates mitochondrial metabolism and proliferative capacity in human ovarian granulosa cells by inducing changes in metabolic substrate utilization.

Paulina Głód, Weronika Marynowicz, Joanna Smoleniec, Dawid Maduzia, Anna Ptak

Abstract read
In one paragraph

Article in Archives of toxicology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Paulina GłódLaboratory of Physiology and Toxicology of Reproduction, Institute of Zoology and Biomedical Research, Faculty of Biology, Jagiellonian University, Gronostajowa 9, 30-387, Krakow, Poland.
Weronika MarynowiczLaboratory of Physiology and Toxicology of Reproduction, Institute of Zoology and Biomedical Research, Faculty of Biology, Jagiellonian University, Gronostajowa 9, 30-387, Krakow, Poland.
Joanna SmoleniecLaboratory of Physiology and Toxicology of Reproduction, Institute of Zoology and Biomedical Research, Faculty of Biology, Jagiellonian University, Gronostajowa 9, 30-387, Krakow, Poland.
Dawid MaduziaInfertility Treatment Centre PARENS, al. 29 Listopada 155C, 31-406, Krakow, Poland.
Anna PtakLaboratory of Physiology and Toxicology of Reproduction, Institute of Zoology and Biomedical Research, Faculty of Biology, Jagiellonian University, Gronostajowa 9, 30-387, Krakow, Poland. anna.ptak@uj.edu.pl.ORCID 0000-0003-3634-1918

Funding

Uniwersytet Jagielloński w Krakowie U1U/W18/NO/28.45
6 · The paper itself

Abstract

The new generation of bisphenols, including bisphenol AF (BPAF), B (BPB), P (BPP) and Z (BPZ), has been detected within the environment of human ovarian follicles. It is therefore hypothesized that these bisphenols may interact directly with ovarian granulosa cells (GCs), which have high metabolic and proliferative activity that is crucial for oocyte development. Therefore, this study aimed to evaluate the effects of environmentally relevant concentrations (0.1–10 nM) of BPB, BPAF, BPP and BPZ on the mitochondrial function, metabolic fuel utilization and proliferation capacity of human GCs. While all bisphenols significantly increased GCs’ proliferation after a single (24 h) treatment, only BPZ enhanced its effect after subsequent (48 h) exposure. Simultaneously, BPZ increased ATP production, and this effect was accompanied by significant disruptions to substrate oxidation. Exposure to BPZ notably shifted metabolism from glucose and glutamine toward fatty acids and increased mRNA expression of peroxisome proliferator‑activated receptors α and δ. Additionally, glutamine and glucose were identified as the primary metabolic fuels that support basal and BPZ-induced proliferation of GCs. The results of this study demonstrate that BPZ disrupts the metabolic flexibility of GCs and stimulates their extensive proliferation. This can have a detrimental effect on follicular development, which in turn can affect ovulation and fertility.

Indexed as

Benzhydryl CompoundsCell ProliferationGranulosa CellsMitochondriaPhenolsAdenosine TriphosphateBisphenol A CompoundsBisphenol B CompoundsCells, CulturedDose-Response Relationship, DrugFemaleGlucoseHumansAdenosine TriphosphateBenzhydryl CompoundsBisphenol A CompoundsBisphenol B CompoundsGlucosePhenolsATP productionHuman ovarian granulosa cellMetabolic fuelsNew generation bisphenols

Identifiers

PMID41428223
PMCPMC13043577

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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 OpenQuestion graph.