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吸入镍纳米颗粒通过线粒体损伤对雄性生殖系统的暴露效应。

Exposure effects of inhaled nickel nanoparticles on the male reproductive system via mitochondria damage.

机构信息

Key Laboratory of Environmental Medicine and Engineering, Ministry of Education; School of Public Health, Southeast University, Nanjing 210009, PR China.

Key Laboratory of Environmental Medicine and Engineering, Ministry of Education; School of Public Health, Southeast University, Nanjing 210009, PR China.

出版信息

NanoImpact. 2021 Jul;23:100350. doi: 10.1016/j.impact.2021.100350. Epub 2021 Aug 11.

DOI:10.1016/j.impact.2021.100350
PMID:35559828
Abstract

Nickel nanoparticles (Ni NPs) have a wide range of application prospects, however there is still a lack of their safety evaluation for the reproductive system. Nowadays, male reproductive health has been widely concerned for the increasing incidence of male infertility. To investigate the male reproductive toxicity induced by Ni NPs and its relation with the mitochondrial fission and mitophagy, male mice were administered with or without 5, 15, and 45 mg/kg of Ni NPs by intratracheal instillation. At the end of intervention, sex hormone level, sperm abnormality rate, pathological morphology of testis, cell apoptosis and the expression levels of Drp1, Pink1 and Parkin proteins in testis tissues were detected. The results indicated that the rate of sperm deformity and serum levels of reproductive hormones increased obviously with the increasing concentrations of Ni NPs. Testicular spermatogenic cells were damaged and the number of apoptotic cells increased significantly. Furthermore, the expressions of key proteins (Drp1, Pink1 and Parkin) related to mitochondrial fission/autophagy in testis tissues also increased after exposure to Ni NPs. Collectively, mitochondria damage may play an important role in male mice reproductive toxicity induced by the intratracheal instillation of Ni NPs.

摘要

镍纳米颗粒(Ni NPs)具有广泛的应用前景,但对于其生殖系统的安全性评估仍缺乏研究。如今,男性生殖健康越来越受到关注,因为男性不育的发病率不断上升。为了研究 Ni NPs 诱导的雄性生殖毒性及其与线粒体分裂和线粒体自噬的关系,通过气管内滴注的方式给雄性小鼠染毒 5、15 和 45mg/kg 的 Ni NPs。干预结束时,检测血清性激素水平、精子畸形率、睾丸组织病理形态、细胞凋亡以及睾丸组织中 Drp1、Pink1 和 Parkin 蛋白的表达水平。结果表明,随着 Ni NPs 浓度的增加,精子畸形率和血清生殖激素水平明显升高,睾丸生精细胞受损,凋亡细胞数量明显增加。此外,Ni NPs 染毒后睾丸组织中与线粒体分裂/自噬相关的关键蛋白(Drp1、Pink1 和 Parkin)的表达也增加。综上所述,线粒体损伤可能在 Ni NPs 气管内滴注诱导的雄性小鼠生殖毒性中发挥重要作用。

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