Polystyrene nanoplastics exposure causes erectile dysfunction in rats

Polystyrene nanoplastics (PS-NPs), emerging and increasingly pervasive environmental contaminants, have the potential to cause persistent harm to organisms. Although previous reports have documented local accumulation and adverse effects in a variety of major organs after PS-NPs exposure, the impact...

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Veröffentlicht in:Ecotoxicology and environmental safety 2024-07, Vol.280, p.116551, Article 116551
Hauptverfasser: Wang, Ming, Dai, Bangshun, Liu, Qiushi, Wang, Xiaobin, Xiao, Yunzheng, Zhang, Guilong, Jiang, Hui, Zhang, Xiansheng, Zhang, Li
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Sprache:eng
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Zusammenfassung:Polystyrene nanoplastics (PS-NPs), emerging and increasingly pervasive environmental contaminants, have the potential to cause persistent harm to organisms. Although previous reports have documented local accumulation and adverse effects in a variety of major organs after PS-NPs exposure, the impact of PS-NPs exposure on erectile function remains unexplored. Herein, we established a rat model of oral exposure to 100 nm PS-NPs for 28 days. To determine the best dose range of PS-NPs, we designed both low-dose and high-dose PS-NPs groups, which correspond to the minimum and maximum human intake doses, respectively. The findings indicated that PS-NPs could accumulate within the corpus cavernosum and high dose but not low dose of PS-NPs triggered erectile dysfunction. Moreover, the toxicological effects of PS-NPs on erectile function include fibrosis in the corpus cavernous, endothelial dysfunction, reduction in testosterone levels, elevated oxidative stress and apoptosis. Overall, this study revealed that PS-NPs exposure can cause erectile dysfunction via multiple ways, which provided new insights into the toxicity of PS-NPs. •Polystyrene nanoplastics (PS-NPs) can locally accumulate in corpus cavernosum.•PS-NPs exposure leads to erectile dysfunction via distinct mechanisms.•PS-NPs exposure causes fibrosis and impairs endothelial function in corpus cavernous.•PS-NPs exposure causes elevated oxidative stress and apoptosis in corpus cavernous.
ISSN:0147-6513
1090-2414
1090-2414
DOI:10.1016/j.ecoenv.2024.116551