纳米氧化铈对48h睡眠剥夺小鼠生精能力的影响
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  • 英文篇名:Effects of Cerium Oxide Nanoparticles on Spermatogenic Function of 48h Sleep Deprived Male Mice
  • 作者:叶铭康 ; 严佳怡 ; 储徐君 ; 葛夏 ; 邹丹 ; 金琎 ; 秦粉菊
  • 英文作者:Ye Mingkang;Yan Jiayi;Chu Xujun;Ge Xia;Zou Dan;Jin Jin;Qin Fenju;Department of Bioscience Technology, Suzhou University of Science and Technology;
  • 关键词:纳米氧化铈 ; 睡眠剥夺 ; 生精能力 ; 睾丸标志酶 ; 抗氧化
  • 英文关键词:CeO2NPs;;Sleep deprivation;;Spermatogenic function;;Marker enzyme;;Antoxidation
  • 中文刊名:GXNB
  • 英文刊名:Genomics and Applied Biology
  • 机构:苏州科技大学生物科学技术研究室;
  • 出版日期:2019-04-25
  • 出版单位:基因组学与应用生物学
  • 年:2019
  • 期:v.38
  • 基金:中国博士后基金(No.2016M601883);; 国家自然科学基金面上项目(No.81773463);; 苏州市科技计划项目(No.SNG2017055);; 江苏省大学生创新创业训练计划共同资助
  • 语种:中文;
  • 页:GXNB201904018
  • 页数:7
  • CN:04
  • ISSN:45-1369/Q
  • 分类号:135-141
摘要
为了研究纳米氧化铈(cerium oxide nanoparticles, CeO2NPs)对48 h睡眠剥夺小鼠生精能力的影响,并探讨其作用机制。将36只6周龄雄性健康清洁级ICR小鼠分为6组:空白对照组、溶剂对照组、睡眠剥夺对照组、CeO2NPs低、中、高剂量组。CeO2NPs低、中、高剂量组分别以4 mg/kg、8 mg/kg和16 mg/kg灌胃1 m L的纳米氧化铈溶液,溶剂对照组和睡眠剥夺对照组灌胃等量溶剂,空白对照组灌胃等量蒸馏水,连续30 d。第31天,采用单平台水环境法进行48 h睡眠剥夺。继之,测定小鼠每日精子生成量、睾丸组织内标志酶(G6PDH,LDH和ACP)及抗氧化指标(CAT, MDA和T-AOC)。与溶剂对照组比较,48 h睡眠剥夺使小鼠睾丸每日精子生成量降低,睾丸标志酶G6PDH、ACP和LDH活力下调,睾丸组织CAT活力和T-AOC水平降低,小鼠睾丸MDA含量升高。与睡眠剥夺对照组比较,CeO2NPs低、中、高剂量组均改善了48 h睡眠剥夺小鼠的每日精子生成量,其中中剂量组的改善更为明显,且在调节睡眠剥夺小鼠睾丸标志酶G6DPH、LDH和ACP活力、提高睾丸组织内CAT活力、T-AOC水平及降低MDA含量方面最为显著。纳米氧化铈可以改善睡眠剥夺雄性小鼠的生精能力,这可能与提高了睾丸组织的抗氧化能力,从而改善了氧化应激损伤并调节了能量消耗代谢有关。
        To study the effects of cerium oxide nanoparticles(CeO2 NPs) on spermatogenic function in 48 hours of sleep deprived male mice and explore its mechanism. Thirty-six healthy clean ICR male mice(six weeks old) were randomly divided into 6 groups: blank control group, solvent control group, sleep deprivation control group, low,medium and high dose groups of CeO2 NPs. 1 m L CeO2 NPs solvent(4 mg/kg, 8 mg/kg and 16 mg/kg) was administered to mice of low, medium and high dose groups of CeO2 NPs, respectively. Solvent control and sleep deprivation control group were given with equivalent solvent, Blank group was given with equivalent distilled water. Intragastric administration continued for 30 days. On the 31 st day, a single platform water environment method was used for48 hours of sleep deprivation on mice. For every animal, daily sperm production, marker enzymes of testis(G6 PDH,LDH, ACP) and the antioxidant of testis tissue(CAT, MDA, T-AOC) were measured. Compared with the solvent con trol group, 48 h sleep deprivation reduced daily sperm production of mice, the activities of G6 PDH, ACP,LDH, CAT, T-AOC level, but increased the content of MDA in testis tissue. Compared with the sleep deprivation control group, the low, medium and high dose groups of CeO2 NPs improved the daily sperm production of 48 h sleep deprived mice. In three dose groups, the middle dose group had the best effect in curbing the adverse impacts of sleep deprivation on daily sperm production and the activity of G6 DPH, LDH and ACP in testis. At the same time, the middle dose has the most significant effect in improving the level of T-AOC in testis and decreasing the content of MDA. CeO2 NPs can improve the spermatogenic function of sleep deprived male mice, the mechanism of which might be involved in increasing antioxidant function,decreasing the damage of free radicals on testis and adjusting the energy metabolism of testis.
引文
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