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苏莉, 邓渊韬, 张瑞, 李成云, 李晋. 硫酸镍对大鼠睾丸细胞损伤作用[J]. 中国公共卫生, 2011, 27(12): 1597-1598. DOI: 10.11847/zgggws2011-27-12-41
引用本文: 苏莉, 邓渊韬, 张瑞, 李成云, 李晋. 硫酸镍对大鼠睾丸细胞损伤作用[J]. 中国公共卫生, 2011, 27(12): 1597-1598. DOI: 10.11847/zgggws2011-27-12-41
SU Li, DENG Yuan-tao, ZHANG Rui, . Toxic mechanisms of nickel sulfate in rat testicular cells[J]. Chinese Journal of Public Health, 2011, 27(12): 1597-1598. DOI: 10.11847/zgggws2011-27-12-41
Citation: SU Li, DENG Yuan-tao, ZHANG Rui, . Toxic mechanisms of nickel sulfate in rat testicular cells[J]. Chinese Journal of Public Health, 2011, 27(12): 1597-1598. DOI: 10.11847/zgggws2011-27-12-41

硫酸镍对大鼠睾丸细胞损伤作用

Toxic mechanisms of nickel sulfate in rat testicular cells

  • 摘要: 目的 探讨硫酸镍(NiSO4)对雄性大鼠生殖系统损伤的可能机制。方法 选择雄性大鼠32只,随机分为4组,对照组,NiSO41.25、2.50、5.00 mg/kg组;采集附睾和睾丸样本,分别检测精子活率和密度,睾丸细胞活性氧自由基(ROS)荧光强度及其Bax、caspase-3蛋白表达水平。结果 NiSO42.50和5.00 mg/kg组大鼠精子活率(分别为68.29%、65.29%)和密度(分别为3.03、2.85×106/mL)均明显低于对照组(82.34%和4.80×106/mL)(P<0.05);睾丸细胞ROS荧光强度(98.59和96.43)则明显高于对照组(62.54)(P<0.01)。与对照组比较,NiSO42.50和5.00mg/kg组Bax蛋白表达量明显升高(P<0.01),各NiSO4组大鼠睾丸细胞caspase-3前体蛋白表达量明显升高(P<0.05),且均出现caspase-3切割片段,后者呈剂量效应关系。结论 过量NiSO4暴露可诱导睾丸细胞内大量生成ROS,进而上调Bax蛋白表达并激活caspase-3蛋白,终致生殖损伤发生。

     

    Abstract: Objective To assess the toxicity of nickel sulfate(NiSO4) on the testes of male rats.Methods The Wistar rats were treated with various concentrations of NiSO4 (0,1.25,2.50,and 5.00 mg/kg/day) for 30 days.Then,sperm motility,reactive oxygen species(ROS) in testicular cells,and the expression of Bax and caspase-3 protein were detected.Results Significant decreases in sperm motility and density of spermatozoa(ρ) in the 2.50 and 5.00 mg NiSO4 groups were observed compared with the control group(P< 0.05).In contrast,intratestiular ROS and the expression of Bax were increased in 2.50 and 5.00 mg NiSO4 groups compared with the controls (P< 0.01).At the same time,pro-caspase-3 protein increased significantly and cleaved-caspase-3 protein expression occured in all NiSO4 exposure groups.Furthermore,the expression of cleaved-caspase-3 protein increased in a dose-dependent manner in all NiSO4 groups.Conclusion NiSO4 at concentrations of 2.50 and 5.00 mg exhibits reproductive toxicity in rats by decreasing sperm.Furthermore,intratesticular ROS,Bax,pro-caspase-3 and cleaved-caspase-3 overexpression play pivotal roles in reproductive damage induced by NiSO4.

     

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