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钛纳米颗粒对小鼠睾丸功能的双向不良反应。

Biphasic adverse effect of titanium nanoparticles on testicular function in mice.

机构信息

Industrial Toxicology and Health Effects Research Group, Japan National Institute of Occupational Safety and Health, 6-21-1 Nagao, Tama-ku, Kawasaki, Kanagawa pref., 214-8585, Japan.

Division of Human Environmental Science, Mount Fuji Research Institute, Yamanashi Prefectural Government, 5597-1 Kenmarubi, Kamiyoshida, Fujiyoshida, Yamanashi pref., 403-0005, Japan.

出版信息

Sci Rep. 2019 Oct 7;9(1):14373. doi: 10.1038/s41598-019-50741-9.

Abstract

The male reproductive system is being recognized as toxic targets of nanoparticles including titanium dioxide nanoparticles (TiNP). Most of these reports are, however, obtained from the results of long-term exposure of TiNP. In this study, we diversely examined the acute effects of TiNP on the male reproductive system. Male C57BL/6J mice were administered a single intravenous injection of TiNP (10, 50 mg/kg), and were sacrificed at 1, 3, and 9 days post-injection. Testicular functions (estimated by sperm motility and sperm number) were measured via computer-assisted sperm analysis (CASA). Results indicated that sperm motility was significantly reduced from 1 day following TiNP injection (in both dose), and this reduction persisted up to 9 days post-TiNP injection (10 mg/kg injection group). Interestingly, we observed no significant decrease in sperm numbers in both the testis and the cauda epididymis in either treatment groups during the course of the experiment. Therefore, we hypothesized that TiNP may target the mature spermatozoa. In addition, sperm suspensions directly incubated with TiNP showed reduced sperm motility, [H]-thymidine incorporation, and ATP level. Our results indicated that TiNP possesses "biphasic effects"; the obstacles to mature sperms (short term effect) in addition to the impairment in testis (long-term effect).

摘要

男性生殖系统正被认为是纳米颗粒(包括二氧化钛纳米颗粒,TiNP)的毒性靶标。然而,这些报告大多是通过 TiNP 的长期暴露结果得出的。在这项研究中,我们广泛研究了 TiNP 对雄性生殖系统的急性影响。雄性 C57BL/6J 小鼠接受单次静脉注射 TiNP(10、50mg/kg),并在注射后 1、3 和 9 天处死。通过计算机辅助精子分析(CASA)测量睾丸功能(通过精子活力和精子数量估计)。结果表明,精子活力从 TiNP 注射后 1 天(在两个剂量组中)显著降低,这种降低持续到 TiNP 注射后 9 天(10mg/kg 注射组)。有趣的是,在实验过程中,两个处理组的睾丸和附睾尾部的精子数量均未见明显减少。因此,我们假设 TiNP 可能靶向成熟的精子。此外,直接与 TiNP 孵育的精子悬浮液显示精子活力、[H]-胸苷掺入和 ATP 水平降低。我们的结果表明,TiNP 具有“双相作用”;除了对睾丸的损害(长期效应)之外,还对成熟精子(短期效应)造成障碍。

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