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Exploring the Activation of the Keap1-Nrf2-ARE Pathway by PAHs in Children's Toys
Jonas Lauenstein1, Simon van de Weyer1, Rasha Alsaleh1
1Institute and Outpatient Clinic of Occupational, Social, and Environmental Medicine, Friedrich-Alexander-University of Erlangen-Nuremberg, Erlangen, Germany.
Insights
Polycyclic aromatic hydrocarbons (PAHs) in toys pose a skin sensitization risk. Benzo[k]fluoranthene, benzo[b]fluoranthene, and chrysene show higher risks, with mixtures exhibiting synergistic effects.
Area of Science:
- Environmental toxicology
- Dermatology
- Chemical risk assessment
Background:
- Children's susceptibility to environmental pollutants.
- Polycyclic Aromatic Hydrocarbons (PAHs) are common in children's toys.
- Assessing skin sensitization risk from PAHs is crucial.
Purpose of the Study:
- Evaluate skin sensitization potential of PAHs using the KeratinoSens assay.
- Investigate the activation of the Keap1-Nrf2-ARE pathway by individual PAHs and their mixtures.
- Determine the risk posed by PAHs in consumer products.
Main Methods:
- KeratinoSens assay on human keratinocytes.
- Assessment of 15 individual PAHs and ternary mixtures.
- Application of concentration addition model and additive index for mixture analysis.
Main Results:
- Benzo[k]fluoranthene (B[k]F) showed the highest potency, 34-fold greater than benzo[a]pyrene (B[a]P).
- Benzo[b]fluoranthene (B[b]F), chrysene, and B[a]P also significantly activated the pathway.
- PAH mixtures demonstrated synergistic effects, indicating amplified risk.
Conclusions:
- B[k]F, B[b]F, and chrysene may present a higher skin sensitization risk than previously recognized.
- Synergistic effects in PAH mixtures necessitate consideration of combined exposures.
- Findings inform risk assessment for PAHs in consumer products, especially toys.
Background:
Children are particularly susceptible to environmental pollutants. This study assessed the skin sensitisation risk associated with polycyclic aromatic hydrocarbons (PAHs), prevalent in toys.
Objectives:
To evaluate the skin sensitisation potential of PAHs using the KeratinoSens assay.
Methods:
Individual PAHs (acenaphthylene, anthracene, benzo[a]anthracene, benzo[a]pyrene (B[a]P), benzo[b]fluoranthene (B[b]F), benzo[e]pyrene, benzo[g,h,i]perylene, benzo[k]fluoranthene (B[k]F), chrysene, fluoranthene, fluorene, naphthalene, phenanthrene, pyrene and triphenylene) and ternary mixtures containing B[a]P were assessed for their ability to activate the Keap1-Nrf2-ARE pathway in human keratinocytes. The concentration addition model and additive index were used to predict and analyse mixture effects.
Results:
Among the individual PAHs, B[k]F demonstrated the most potent activation of the pathway, exhibiting a 34-fold higher potency relative to B[a]P. B[b]F, chrysene and B[a]P also exhibited significant activation, while the remaining PAHs displayed negligible or weak activation. Notably, PAH mixtures exhibited synergistic effects, except for those composed solely of potent sensitizers.
Conclusions:
This study provides the first assessment of the skin sensitization potential of these PAHs. The findings suggest that B[k]F, B[b]F and chrysene may pose a higher risk of skin sensitisation than previously thought. Additionally, the synergistic effects observed in mixtures highlight the importance of considering combined exposures when assessing PAH exposure risk.
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