4.2 Article

Sex-Dependent Bioaccumulation of Nano Zinc Oxide and Its Adverse Effects on Sexual Behavior and Reproduction in Japanese Medaka

期刊

ACS APPLIED BIO MATERIALS
卷 4, 期 10, 页码 7408-7421

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsabm.1c00575

关键词

engineered nanoparticles; nano zinc oxide; biodistribution; reproduction; endocrine disruption

资金

  1. Department of Biotechnology [BT/PR14920/NNT/28/503/2010]
  2. Nanomission, Department of Science and Technology [SR/NM/NS-1070/2012]
  3. DST-Inspire Fellowship [DST/INSPIRE fellowship/2013/122]
  4. Department of Science and Technology
  5. National BioResource Project, Japan
  6. Sophisticated Tests and Instrumentation Centre (STIC)

向作者/读者索取更多资源

This study found that the toxic effects of nZnO on the reproductive system were mainly caused by ROS induction, while zinc ions were predominantly responsible for the adverse impact of ZnSO4. Exposure to nZnO in males affected sexual behavior and fertility, while in females it caused ovarian issues and changes in sex steroid levels.
This study investigated the adverse effects of 200 nm zinc oxide particles (nZnO) on sexual behavior and reproduction in Japanese medaka in comparison with ZnSO4 and correlated the consequences with the bioaccumulation pattern of the particles in associated organs. nZnO exposure impaired sexual and territorial behaviors and affected fertility by altering sperm viability and motility in males through reactive oxygen species (ROS) induction. Conversely, none of these effects other than behavior loss was seen in males exposed to ZnSO4. nZnO exposure to females induced ROS in ovaries, causing follicular growth arrest, atresia, and subfertility. Further, sexsteroid levels were altered by both nZnO and ZnSO4 in males and by nZnO but not ZnSO4 in females. Biodistribution studies revealed the deposition of nZnO as particulate matter in the brain, gills, gut, kidney, and ovary. Particle accumulation in the brain was sex specific, as the particles were found in the brain of males but not that of females. A similar trend was seen for zinc levels in males and females exposed to ZnSO4. Importantly, the female sex hormone, 17 beta-estradiol was found to prevent nZnO accumulation in the female brain, emphasizing the need for biodistribution profiling of nanoparticle-based drug delivery vehicles separately in males and females before they are commercialized. This study has demonstrated that the toxic effects of nZnO on the reproductive system were mainly caused by ROS induction, while zinc ions were predominantly responsible for the adverse impact of ZnSO4.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.2
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据