College of Animal Science and Veterinary Medicine, Shanxi Agricultural University, Taigu, Shanxi, China.
Shanxi Key Laboratory of Ecological Animal Science and Environmental Veterinary Medicine, Taigu, Shanxi, China.
Biol Trace Elem Res. 2018 Jul;184(1):148-153. doi: 10.1007/s12011-017-1181-1. Epub 2017 Oct 8.
Oxidative damage has been implicated to be one of main mechanisms by which fluoride (F) induces toxic effects. Previous studies reported that F destroyed the epididymal structure of mouse and rabbit. Epididymis is the important place for sperm maturation. However, little is known about the effect of F on the oxidative stress status of epididymis. Therefore, the aim of the present study was to explore the changes in the activities and transcriptional levels of CuZn superoxide dismutase (CuZn-SOD, SOD1) and catalase (CAT), as well as the ultrastructure, in testis and epididymis of mice administrated with F. Sixty health Kunming mice were randomly divided into four groups. With one group untreated as controls, the others were treated with 25, 50, and 100 mg NaF/L in drinking water. After 10 weeks administration, mitochondrial ultrastructural changes in testis and epididymis were observed, including the incomplete membrane and the dissolved or disappeared cristae. Compared to the control group, the activities of both SOD1 and CAT in testis and epididymis were significantly reduced by 50 or 100 mg NaF exposure. In addition, the mRNA expressions of testicular SOD1 and CAT were also decreased significantly in 100 mg NaF/L group, while the SOD1 and CAT mRNA expressions in epididymides were significantly reduced in all F treatment groups. The above results suggest that in the presence of F, similar to testis, epididymis also loses the balance between oxidative stress and antioxidative defense, and perhaps more sensitive to F.
氧化损伤被认为是氟(F)诱导毒性作用的主要机制之一。先前的研究报道,F 破坏了小鼠和兔子的附睾结构。附睾是精子成熟的重要场所。然而,关于 F 对附睾氧化应激状态的影响知之甚少。因此,本研究旨在探讨 F 处理后小鼠睾丸和附睾中 CuZn 超氧化物歧化酶(CuZn-SOD,SOD1)和过氧化氢酶(CAT)的活性和转录水平以及超微结构的变化。60 只健康昆明小鼠随机分为四组。一组不处理作为对照组,其余三组分别用 25、50 和 100mg/L NaF 处理饮用水。处理 10 周后,观察睾丸和附睾中线粒体的超微结构变化,包括膜不完整和嵴溶解或消失。与对照组相比,50 或 100mg/L NaF 暴露使睾丸和附睾中 SOD1 和 CAT 的活性均显著降低。此外,100mg/L NaF/L 组睾丸 SOD1 和 CAT 的 mRNA 表达也显著降低,而所有 F 处理组附睾中 SOD1 和 CAT 的 mRNA 表达均显著降低。上述结果表明,在 F 的存在下,附睾与睾丸一样,也失去了氧化应激和抗氧化防御之间的平衡,并且可能对 F 更敏感。