期刊
PARTICLE AND FIBRE TOXICOLOGY
卷 19, 期 1, 页码 -出版社
BMC
DOI: 10.1186/s12989-022-00453-2
关键词
PS-MPs; Reproductive toxicity; Testosterone; LHR
类别
资金
- Natural Science Foundation of Jiangsu Province of China [BK20190316]
- Fundamental Research Funds for the Central Universities [0214-14380438, 0214-14380471]
- National Natural Science Foundation of China [31870492, 31901182, 31971517]
Chronic exposure to microplastics can lead to reproductive abnormalities in mammals, including changes in testicular morphology, abnormal spermatogenesis, and interference with hormone secretion in the serum.
Background: Microplastics (MPs), which are smaller in size and difficult to degrade, can be easily ingested by marine life and enter mammals through the food chain. Our previous study demonstrated that following acute exposure to MPs, the serum testosterone content reduced and sperm quality declined, resulting in male reproductive dysfunction in mice. However, the toxic effect of long-term exposure to MPs at environmental exposure levels on the reproductive system of mammals remains unclear. Results: In vivo, mice were given drinking water containing 100 mu g/L and 1000 mu g/L polystyrene MPs (PS-MPs) with particle sizes of 0.5 mu m, 4 mu m, and 10 mu m for 180 consecutive days. We observed alterations in testicular morphology and reductions in testosterone, LH and FSH contents in serum. In addition, the viability of sperm was declined and the rate of sperm abnormality was increased following exposure to PS-MPs. The expression of steroidogenic enzymes and StAR was downregulated in testis tissues. In vitro, we used primary Leydig cells to explore the underlying mechanism of the decrease in testosterone induced by PS-MPs. First, we discovered that PS-MPs attached to and became internalized by Leydig cells. And then we found that the contents of testosterone in the supernatant declined. Meanwhile, LHR, steroidogenic enzymes and StAR were downregulated with concentration-dependent on PS-MPs. We also confirmed that PS-MPs decreased StAR expression by inhibiting activation of the AC/cAMP/PKA pathway. Moreover, the overexpression of LHR alleviated the reduction in StAR and steroidogenic enzymes levels, and finally alleviated the reduction in testosterone induced by PS-MPs. Conclusions: PS-MPs exposure resulted in alterations in testicular histology, abnormal spermatogenesis, and interference of serum hormone secretion in mice. PS-MPs induced a reduction in testosterone level through downregulation of the LH-mediated LHR/cAMP/PKA/StAR pathway. In summary, our study showed that chronic exposure to PS-MPs resulted in toxicity of male reproduction under environmental exposure levels, and these potential risks may ring alarm bells of public health.
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