ArticleEnvironmental toxicology and chemistry2025
Bioconcentration, maternal transfer, and toxicokinetics of PFOS in a multi-generational zebrafish exposure.
Article in Environmental toxicology and chemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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.
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.
Who cites it
3 citing papers in PubMed.
- Review
- Pattern of Detections Across Multiple Environmental Messenger RNAs (e-mRNAs) in Stressor-Exposed Zebrafish (Ecology and evolution · 2026Article
- Toxicokinetic Profiling and Developmental Toxicity of Long-Chain Per- and Polyfluoroalkyl Substances in Zebrafish.Environmental science & technology · 2025Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
10 authors.
Funding
Abstract
To enable risk characterization of perfluorooctane sulfonic acid (PFOS) in extended chronic and multi-generational exposures, we assessed PFOS bioconcentration in zebrafish (Danio rerio) exposed continuously to environmentally-relevant PFOS concentrations (0, 0.1, 0.6, 3.2, 20, and 100 µg/L PFOS) through 180 days postfertilization (dpf) in parental (P) and first filial generation (F1) fish. Exposures included five replicate tanks per treatment where whole-body PFOS concentrations were measured using 20-35 fish per replicate at 14 and 29 dpf in the P generation and one fish of each sex per replicate at 180 dpf for the P and F1 generations. Perfluorooctane sulfonic acid accumulation reached an apparent steady state at ≤ 14 dpf where whole-body wet-weight concentrations remained constant through 180 dpf in the P and F1 generations. The median bioconcentration factor (BCF) of 934 L/kg was observed for all PFOS exposures with a range from 255 to 2,136 L/kg which varied with PFOS exposure concentration and sex of adult fish. Significantly lower BCFs were observed in 20 and 100 µg/L PFOS exposures versus 0.1 and 0.6 µg/L indicating exposure-concentration dependance. Additionally, males had significantly increased (∼2×) PFOS accumulation and BCFs versus females in both P and F1 generations. Maternal transfer of PFOS was observed from P females to F1 eggs where maternal whole-body and egg PFOS burdens were equivalent, suggesting PFOS transfer to eggs was not a depuration pathway. Finally, a toxicokinetic model was developed that reliably reproduced PFOS whole-body burdens (data within 1.64-fold of predicted values) across all exposure durations spanning the P and F1 generations, providing a tool for PFOS bioaccumulation predictions relevant for risk assessment of acute, chronic, and multi-generational exposures.
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Registered trials
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.