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Maternal exposure to polystyrene nanoplastics during gestation and lactation induces hepatic and testicular toxicity in male mouse offspring

Food and Chemical Toxicology 2022 168 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 60 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Zhangbei Sun, Tao Huang, Zhangbei Sun, Tao Huang, Shujuan Liu, Yangyang Yuan, Wenjuan Zhang Tingting Lin, Shujuan Liu, Shujuan Liu, Shujuan Liu, Yangyang Yuan, Zhangbei Sun, Bei Yang, Bei Yang, Fangming Liu, Haibin Kuang, Haibin Kuang, Tingting Lin, Tingting Lin, Haibin Kuang, Dalei Zhang, Yangyang Yuan, Yangyang Yuan, Yangyang Yuan, Xiting Xiang, Yangyang Yuan, Haibin Kuang, Yangyang Yuan, Dalei Zhang, Bei Yang, Dalei Zhang, Dalei Zhang, Dalei Zhang, Wenjuan Zhang

Summary

Researchers exposed pregnant and nursing mice to polystyrene nanoplastics and studied the effects on their male offspring. The offspring showed reduced body weight, liver damage with inflammation and disrupted sugar metabolism, and testicular harm including decreased sperm counts. The findings suggest that nanoplastic exposure during pregnancy and breastfeeding can cause significant organ damage in the next generation.

Nanoplastics have raised considerable concerns since their ubiquity in the environment and potential hazard to health. It has been proven that polystyrene nanoparticles (PS-NPs) can be maternally transferred to the offspring. In this study, mice were exposed gestationally and lactationally to PS-NPs (size 100 nm) at different doses (0.1, 1 and 10 mg/L) to investigate the trans-generational poisonousness. Our data illustrated that maternal PS-NPs exposure in pregnancy and lactation resulted in a decline in birth and postnatal body weight in offspring mice. Furthermore, high-dose PS-NPs reduced liver weight, triggered oxidative stress, caused inflammatory cell infiltration, up-regulated proinflammatory cytokine expression, and disturbed glycometabolism in the liver of male offspring mice. In addition, pre- and postnatal PS-NPs exposure diminished testis weight, disrupted seminiferous epithelium and decreased sperm count in mouse offspring. Moreover, PS-NPs induced testicular oxidative injury, as presented by increased malondialdehyde generation and altered superoxide dismutase and catalase activities in the testis of offspring mice. These findings declared that maternal exposure to PS-NPs in pregnancy and lactation can cause hepatic and testicular toxicity in male mouse pups, which put forward new understanding into the detrimental effects of nanoplastics on mammalian offspring.

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