4.7 Article

Comparing the effects of polystyrene microplastics exposure on reproduction and fertility in male and female mice

Journal

TOXICOLOGY
Volume 465, Issue -, Pages -

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.tox.2021.153059

Keywords

Fertility; Microplastics; Polystyrene microplastics; Reproductive toxicity

Funding

  1. National Key Research and Development Program of China [2017YFC0702700]
  2. Fundamental Research Funds for the Central Universities [CCNU20TS020]

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Exposure to microplastics has negative effects on the reproductive systems and fertility of mice. Male mice experience reduced sperm quantity and increased sperm deformity, while female mice experience decreased ovary size and follicle number. Additionally, microplastic exposure alters hormone levels and leads to reduced pregnancy rates and fewer embryos in mice.
Microplastics (MPs) may have an impact on the reproductive development of humans and mammals. However, any effects of MPs exposure on male and female reproductive systems and fertility are still ambiguous. In this study, male and female C57BL/6 mice were exposed to saline or 0.1 mg/d polystyrene microplastics (PS-MPs) for 30 days or 44 days to determine the effects of MPs on reproductive systems, following which some of the mice were caged for 10 days to mate to test fertility. Another group of mice were given fluorescent PS-MPs to determine the accumulation of MPs. The results show that PS-MPs exposure resulted in more significant accumulation and oxidative stress in the ovary than in the testis. In male mice, the number of viable epididymis sperm and spermatogenic cells in the testes after PS-MPs exposure was significantly reduced, and the rate of sperm deformity increased. In female mice, PS-MPs exposure induced a decrease in ovary size and number of follicles. After exposure to PS-MPs, the levels of Follicle stimulating hormone, Luteinizing hormone and testosterone were reduced, and the estradiol levels increased in the serum of male mice, while the changes in these hormone levels of female mice was the opposite. The mice exposed to PS-MPs had a reduced pregnancy rate and produced fewer embryos. These findings suggest that exposure to PS-MPs damaged the testes and ovaries, induced oxidative stress, altered the serum hormone levels, and induced changes in reproduction and fertility. Female mice appear to be more susceptible to MPs in reproduction and fertility than male mice.

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