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Combined exposure to titanium nanoparticles and nanoplastics damages the male reproductive system and sperm activity

Materials Today Bio 2025 Score: 48 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Gang Xiang, Yin Yi, Gang Xiang, A. L. Deng, A. L. Deng, Yunjia Wang, Gang Xiang, Guanteng Yang, Tao Li Jie Dai, S. L. He, Guanteng Yang, Yunjia Wang, Yunjia Wang, Tao Li

Summary

This study assessed the effects of combined TiO2 nanoparticles and polystyrene nanoplastics on male reproductive function in animal models, finding that co-exposure caused greater damage to sperm motility, testicular structure, and hormone levels than either material alone. The results raise concerns about combined environmental exposure to two common industrial nanomaterials.

Polymers
Body Systems
Study Type In vitro

Plastics (PS) and titanium (Ti) are utilized extensively in industrial, household, and medical applications due to their advantageous physicochemical properties. However, these materials have given rise to growing concerns regarding their biosafety. In this study, we investigated the impact of TiO<sub>2</sub> nanoparticles (TiO<sub>2</sub> NPs) and nanoplastics (nPS) on the reproductive function of male zebrafish (<i>Danio rerio</i>). Following a 30-day exposure period, the accumulation of both TiO<sub>2</sub> NPs and nPS in testicular tissue was observed. Male zebrafish demonstrated significant decreases in secondary sexual characteristics, substantial reductions in sex hormone levels, and impaired sperm quality. While these effects were evident following individual exposures to either TiO<sub>2</sub> NPs or nPS, co-exposure significantly intensified the extent of reproductive toxicity. Furthermore, the offspring of exposed males displayed pronounced developmental toxicity. Subsequent RNA sequencing analysis revealed significant upregulation of apoptosis-related genes in testicular tissue after exposure. Concomitant <i>in vitro</i> investigations employing GC-1 spermatogonial cells substantiated that co-exposure instigated apoptosis, plausibly through the activation of the PPARγ/RIPK3 signaling pathway. Collectively, our findings provide robust evidence that co-exposure to TiO<sub>2</sub> NPs and nPS compromises male zebrafish reproductive function and induces transgenerational developmental toxicity, offering important theoretical insights for the prevention and risk assessment of emerging environmental co-contaminants.

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