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Bisphenol S-induced inflammation: a comparative insight on inflammatory pathway activation in zebrafish and rodent models.

Created on 15 Sep 2026

Authors

Wan Nur Izzati Wan Azhan, Fatin Nadzirah Zakaria, Danial Akmal Fuad Al' Arifin, Nur-Zulaikha Amlie, Evana Kamarudin, Faheze Paiman, Rio Risandiansyah, Razif Dasiman

Published in

Annali dell'Istituto superiore di sanita. Volume 62. Issue 3. Pages 267-276.

Abstract

Bisphenol S (BPS) is a widespread BPA substitute with emerging immunotoxicity; this review synthesizes zebrafish and rodent experimental evidence to clarify BPS-induced inflammation.
Narrative synthesis of experimental studies in zebrafish and rodent models, focusing on molecular pathways, organ-level effects, and exposure timing.
Across models, BPS consistently activates an oxidative stress-mediated NF-κB axis with increased ROS, lipid peroxidation, and upregulation of TNF-α, IL-1β, and IL-6; chronic and developmental low-to-moderate exposures produced stronger inflammatory phenotypes than acute high doses.
Convergent mechanistic and pathological findings strengthen the weight of evidence for BPS immunotoxicity and support targeted monitoring and controls; key research gaps include inflammasome activation, receptor mechanisms, sex differences, mixture effects, epigenetic regulation, and standardization.

PMID:
42742244
Bibliographic data and abstract were imported from PubMed on 15 Sep 2026.

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