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Polystyrene Nanoparticles Cause Sex‐Specific Toxicity in Male Zebrafish, Which Can Be Mitigated by Melatonin

Environmental Toxicology 2026 Score: 50 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Guanglong Chen W. Liu, W. Liu, W. Liu, W. Liu, Guanglong Chen Guanglong Chen Guanglong Chen Chunhua Zhan, Guanglong Chen Guanglong Chen Guanglong Chen Guanglong Chen Guanglong Chen Chunhua Zhan, Chunhua Zhan, Guanglong Chen Guanglong Chen Chunhua Zhan, Guanglong Chen Guanglong Chen Guanglong Chen Guanglong Chen Guanglong Chen Guanglong Chen Guanglong Chen Min Zeng, Guanglong Chen Guanglong Chen Guanglong Chen Guanglong Chen Guanglong Chen Chunhua Zhan, Min Zeng, Guanglong Chen Guanglong Chen Guanglong Chen Guanglong Chen Guanglong Chen Guanglong Chen Jun Wang, Jun Wang, Guanglong Chen Min Zeng, Guanglong Chen Guanglong Chen Guanglong Chen Guanglong Chen Guanglong Chen Guanglong Chen Guanglong Chen Jun Wang, Guanglong Chen Chunhua Zhan, Guanglong Chen Guanglong Chen Chunhua Zhan, Guanglong Chen Chunhua Zhan, Guanglong Chen Guanglong Chen Chunhua Zhan, Guanglong Chen Guanglong Chen Guanglong Chen Guanglong Chen Guanglong Chen Guanglong Chen Guanglong Chen

Summary

Researchers exposed adult zebrafish to polystyrene nanoparticles for 14 days and found significant reproductive toxicity that was more pronounced in males, including reduced gonadal size and disrupted hormone signaling along the hypothalamic-pituitary-gonadal axis. Co-treatment with melatonin largely reversed these harmful effects by protecting against oxidative damage. The study suggests that melatonin may offer a potential protective strategy against nanoplastic-induced reproductive harm.

Polymers

The environmental ubiquity of microplastics raises growing concerns over their reproductive toxicity, although the underlying molecular mechanisms remain unclear. In this study, adult zebrafish were exposed to polystyrene nanoparticles (PSNPs; 0, 0.1, and 1 mg/L) for 14 days, with or without co-treatment of melatonin (1 μM). Exposure to 1 mg/L PSNPs significantly reduced gonadosomatic and brain somatic indices, accompanied by histopathological evidence of structural damage to gonadal tissues. Moreover, PSNPs disrupted hypothalamic-pituitary-gonadal (HPG) axis gene transcription and altered sex hormone levels. PSNPs also induced oxidative stress and apoptosis in gonadal and brain tissues. Notably, these effects were sex-dependent and were largely ameliorated by melatonin co-treatment. Importantly, PSNPs showed differential reproductive toxicity between males and females. These findings highlight the potential of melatonin to mitigate PSNP-induced reproductive toxicity by protecting against oxidative damage and HPG axis disruption while also revealing sex-specific responses to nanoparticle exposure.

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