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Systematic review of endocrine-disrupting chemicals and neurotoxic effects in zebrafish

Systematic review of endocrine-disrupting chemicals and neurotoxic effects in zebrafish
Photo by Brett Jordan / Unsplash
Key Takeaway
Note potential neurodevelopmental implications of EDCs in vertebrate models, though human relevance remains uncertain.

This systematic review examines the impact of endocrine-disrupting chemicals (EDCs) on zebrafish (Danio rerio) across 12 studies. The scope includes a wide range of substances, such as 6-OH-BDE-47, atrazine, BDE-209, bisphenol (BPA), bisphenol S (BPS), Cd, estrone, OBS, Pb, tributyltin (TBT), TCEP, TDCPP, Thifluzamide (THM), Ti, and binary mixtures like BDE-209 with Pb or BPA with Ti.

The primary outcome assessed was neurotoxic effects, with secondary outcomes including alterations in thyroid and sex steroid hormone levels, neurotransmitter contents, AChE activity, locomotor behavior, gene expression, and intergenerational consequences. The review identifies significant neurodevelopmental endpoints associated with these exposures. However, specific effect sizes, absolute numbers, and p-values were not reported for these findings.

The authors note that the practice relevance lies in emphasizing the relevance of these findings to vertebrate neurodevelopment and the potential implications for human health. Limitations regarding causality, certainty, and specific adverse events were not reported in the source material. Consequently, direct clinical application to human populations cannot be inferred from these zebrafish models without further evidence.

Study Details

Study typeMeta analysis
EvidenceLevel 1
PublishedApr 2026
View Original Abstract ↓
Endocrine-disrupting chemicals (EDCs) are well known for their ability to interfere with endocrine function; however, growing evidence indicates that they can also cause profound neurotoxic effects. These substances can affect both the central and peripheral nervous systems of aquatic organisms, including fish, and can disrupt neurobehavioral development, posing a potential threat to aquatic species. In this systematic review, we examine the neurotoxic effects of EDCs on zebrafish (Danio rerio), a widely utilized model organism for investigating vertebrate nervous system development. A comprehensive bibliographic search was conducted in PubMed using the terms “developmental neurotoxicity” and “fish,” which yielded 603 articles. The search was refined by incorporating the terms “endocrine disruptors” and “zebrafish,” resulting in 15 relevant studies. Of these, three were excluded—two due to irrelevance to the topic and one for being a review on strobilurin, a fungicide. The remaining 12 studies provided insights into the neurotoxic effects of 14 chemicals, including 6-OH-BDE-47 (2,2´,4,4´-tetrabromodiphenyl ether), atrazine, BDE-209, bisphenol (BPA), bisphenol S (BPS), Cd, estrone, OBS, Pb, tributyltin (TBT), tris(2-chloroethyl) phosphate (TCEP), tris(1,3-dichloro-2-propyl) phosphate (TDCPP), Thifluzamide (THM), and Ti. These compounds, encompassing biocides, heavy metals, hormones, brominated compounds, plastic components, and flame retardants, were identified as potential EDCs that disrupt nervous system development and behavior in zebrafish during embryonic, larval, and adult stages. Studies have also investigated co-exposure effects of binary mixtures like BDE-209 with Pb, BPA with Ti, and TBT with Cd. We identified significant neurodevelopmental endpoints, including alterations in thyroid/sex steroid hormone levels; neurotransmitter contents, including dopamine, serotonin, and GABA; AChE activity; locomotor behavior; and expression of sensitive genes and proteins. Notably, these neurotoxic effects were shown to have intergenerational/transgenerational/epigenetic consequences. Overall, this review provides comprehensive evidence of the neurotoxic potential of EDCs on zebrafish, emphasizing their relevance to vertebrate neurodevelopment and the potential implications for human health.
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