Evidence map›Paper›PMID 42545546›Full record

ArticleHistochemistry and cell biology2026

Endoplasmic reticulum stress is associated with cardiac effects of bisphenol S independently of a high-fat diet.

Beatriz Alexandre-Santos, Guilherme Dos Santos Reis, Luiza Mazzali Ferraz, Maria Eduarda Lima da Silva, Gabriel Ferreira Lima, Fernanda Carla Ferreira Brito, Milena Barcza Stockler-Pinto, Antonio Claudio Lucas da Nóbrega, Leandro Miranda-Alves, D'Angelo Carlo Magliano and 1 more

Abstract read
In one paragraph

Article in Histochemistry and cell biology, 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

11 authors.

Beatriz Alexandre-SantosDepartment of Morphology, Laboratory of Exercise Sciences, Biomedical Institute, Fluminense Federal University, Rua Alameda Barros Terra, S/N, Sao Domingos, Niteroi, RJ, 24.020-150, Brazil.
Guilherme Dos Santos ReisDepartment of Morphology, Laboratory of Exercise Sciences, Biomedical Institute, Fluminense Federal University, Rua Alameda Barros Terra, S/N, Sao Domingos, Niteroi, RJ, 24.020-150, Brazil.
Luiza Mazzali FerrazDepartment of Morphology, Laboratory of Exercise Sciences, Biomedical Institute, Fluminense Federal University, Rua Alameda Barros Terra, S/N, Sao Domingos, Niteroi, RJ, 24.020-150, Brazil.
Maria Eduarda Lima da SilvaDepartment of Morphology, Laboratory of Exercise Sciences, Biomedical Institute, Fluminense Federal University, Rua Alameda Barros Terra, S/N, Sao Domingos, Niteroi, RJ, 24.020-150, Brazil.
Gabriel Ferreira LimaLaboratory of Experimental Pharmacology, Biomedical Institute, Fluminense Federal University, Niteroi, RJ, Brazil.
Fernanda Carla Ferreira BritoLaboratory of Experimental Pharmacology, Biomedical Institute, Fluminense Federal University, Niteroi, RJ, Brazil.
Milena Barcza Stockler-PintoResearch Center On Nutrigenetics and Nutrigenomics, Faculty of Nutrition, Fluminense Federal University, Niteroi, RJ, Brazil.
Antonio Claudio Lucas da NóbregaDepartment of Morphology, Laboratory of Exercise Sciences, Biomedical Institute, Fluminense Federal University, Rua Alameda Barros Terra, S/N, Sao Domingos, Niteroi, RJ, 24.020-150, Brazil.
Leandro Miranda-AlvesLaboratory of Experimental Endocrinology, Institute of Biomedical Science, Federal University of Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
D'Angelo Carlo MaglianoResearch Center On Morphology and Metabolism, Biomedical Institute, Fluminense Federal University, Niteroi, RJ, Brazil.
Eliete Dalla Corte FrantzDepartment of Morphology, Laboratory of Exercise Sciences, Biomedical Institute, Fluminense Federal University, Rua Alameda Barros Terra, S/N, Sao Domingos, Niteroi, RJ, 24.020-150, Brazil. elietedcf@id.uff.br.ORCID https://orcid.org/0000-0002-1747-5614

Funding

Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro E-26/010.001841/2019, EDCF; E-26/201.347/2022, EDCF; E-26/210.014/2020, ACLN; E-26/201.293/2022, DCM; E26/211.461/2021, DCM; E-26/201.373/2021, MBSP
6 · The paper itself

Abstract

Obesity and endocrine disruptors (EDs) promote endoplasmic reticulum (ER) stress, a mechanism associated with cardiovascular diseases. Among EDs, BPS is widely used in consumer products. Whether BPS promotes cardiac ER stress, either alone or combined with a high-fat diet, remains unclear. Male C57BL/6 mice were assigned to a standard chow diet (SC-15 kJ/g), SC+BPS (SCB), high-fat diet (HF-21 kJ/g), or HF+BPS (HFB), receiving BPS (25 μg/kg/day) through their drinking water for 12 weeks. Body mass (BM), lipid profile, cardiac risk ratio, heart mass, and cardiac ER stress, apoptosis, and oxidative stress markers were assessed. A high-fat diet intake increased BM gain, total cholesterol, cardiac risk ratio, and heart mass compared with standard chow diet intake. These parameters were higher in the SCB group than in the SC group. ER stress (GRP78, ATF4, and CHOP protein expression), pro-apoptotic (BAX protein expression and caspase 3 immunostaining), and pro-oxidative (NOX2 and NOX4 protein expression as well as MDA levels) markers were elevated in high-fat diet-fed animals compared with standard chow-fed animals. BPS exposure increased these parameters in standard chow-fed animals. High-fat diet intake reduced BCL2 expression and increased the BAX/BCL2 ratio compared with standard chow diet intake. BPS exposure increased BCL2 expression in standard chow-fed animals and increased the BAX/BCL2 ratio in high-fat diet-fed animals. ER stress appears to play a role in the cardiac effects of BPS. BPS exposure exacerbated the high-fat diet-induced pro-apoptotic response.

Indexed as

Diet, High-FatEndoplasmic Reticulum StressHeartPhenolsSulfonesAnimalsApoptosisBisphenol S CompoundsEndoplasmic Reticulum Chaperone BiPMaleMiceMice, Inbred C57BLbisphenol SBisphenol S CompoundsEndoplasmic Reticulum Chaperone BiPHspa5 protein, mousePhenolsSulfonesApoptosisBisphenol SEndoplasmic reticulum stressHeartObesityOxidative stress

Identifiers

PMID42545546
PMCPMC13433454

What Socratic holds

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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.