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纳米硫化镉与硫化镉雄性生殖毒性及相关机制的研究
引用本文:周庆红,姜淑卿,刘英华,张力,赵春红,王晓军,张大龙,张静姝.纳米硫化镉与硫化镉雄性生殖毒性及相关机制的研究[J].癌变.畸变.突变,2014,26(6):441-445.
作者姓名:周庆红  姜淑卿  刘英华  张力  赵春红  王晓军  张大龙  张静姝
作者单位:天津市疾病预防控制中心毒理室,天津 300011
基金项目:天津市应用基础与前沿技术研究计划项目,天津市疾病预防控制中心科技基金项目
摘    要:目的: 探讨纳米硫化镉(Nano-CdS)和硫化镉(CdS)的雄性生殖毒性作用机制并比较其生殖毒性效应。方法:将36只SPF级雄性ICR小鼠随机分为对照组、Nano-CdS组和CdS组,每组各12只。两个染毒组经口灌胃染毒,每天灌胃1次,染毒剂量均为50 mg/kg,对照组给予等体积的生理盐水,连续45 d。采用石墨炉原子吸收光谱法检测小鼠睾丸组织中镉元素积累水平,显微镜下观察小鼠精子畸形率,采用酶联免疫吸附法(ELISA)检测小鼠血清睾酮水平,采用荧光实时定量PCR检测P450scc和P450-17α mRNA表达水平。结果:镉元素含量分析结果显示,Nano-CdS和CdS组小鼠睾丸组织中的镉元素含量分别为(425.46±73.89)和(183.59±32.46) ng/g,均高于对照组的(80.18±13.29) ng/g (P<0.05)。精子畸形率检测结果显示,CdS组小鼠(2.28%)显著高于对照组(1.48%) (P<0.05),Nano-CdS组(1.73%)也有所升高。ELISA检测结果显示,Nano-CdS和CdS组小鼠血清睾酮浓度分别为(12.31± 1.10)和(15.88±5.41)ng/dL,均明显低于对照组的(68.41±11.36) ng/dL(P<0.05)。荧光实时定量PCR检测结果显示,Nano-CdS和CdS组P450scc mRNA的表达水平分别为0.50±0.11和0.84±0.48;P450-17α mRNA的表达水平分别为0.51±0.13和0.72±0.06,除CdS组P450scc mRNA表达水平外,其他各组均明显低于对照组(P<0.05)。结论:Nano-CdS和CdS均能导致小鼠睾丸中镉元素的积累,一定程度上诱导精子畸形率的升高,并能显著降低血清睾酮水平以及抑制P450scc和P450-17α mRNA的表达水平。

关 键 词:纳米硫化镉  精子畸形  睾酮  细胞色素P450  胆固醇侧链裂解酶  类固醇17-&alpha  -羟化酶  
收稿时间:2014-06-09

Study on the toxicity and related machanisms of Nano-CdS and CdS on male reproduction
ZHOU Qing-hong,JIANG Shu-qing,LIU Ying-hua,ZHANG Li,ZHAO Chun-hong,WANG Xiao-jun,ZHANG Da-long,ZHANG Jing-shu.Study on the toxicity and related machanisms of Nano-CdS and CdS on male reproduction[J].Carcinogenesis,Teratogenesis and Mutagenesis,2014,26(6):441-445.
Authors:ZHOU Qing-hong  JIANG Shu-qing  LIU Ying-hua  ZHANG Li  ZHAO Chun-hong  WANG Xiao-jun  ZHANG Da-long  ZHANG Jing-shu
Institution:Toxicology  Laboratory  of  Tianjin  Centers  for  Disease  Control  and  Prevention,  Tianjin  300011,  China
Abstract:OBJECTIVE:To compare the effects of normal cadmium sulfide (CdS) and Nano-CdS on the male reproductive system of mice,and to investigate the mechanisms of reproductive toxicity. METHODS:36 male ICR mice were randomly divided into control group,and two experimental groups which were exposed to 50 mg/kg Nano-CdS and CdS,respectively. Mice in control group were exposed to same volume of physiological saline . After 45 days,levels of cadmium accumulation in testis were determined directly by GF AAS. The rate of sperm abnormality was also calculated. Serum testosterone levels were measured by enzyme-linked immunosorbent assay (ELISA),expression levels of P450scc and P450-17α mRNA were determined by real-time PCR. RESULTS:Contents of cadmium in Nano-CdS and CdS groups were (425.46±73.89) and (183.59±32.46) ng/g,respectively,and were higher than the control (80.18±13.29) (P〈0.05). Sperm deformity rate in CdS group (2.28%) was significantly higher than the control (1.48%) (P〈0.05),Nano-CdS group (1.73%) was also increased. Concentrations of testosterone in CdS and Nano-CdS groups were(12.31±1.10) and (15.88±5.41) ng/dL,respectively,and were significantly lower than control group (68.41±11.36) ng/dL (P〈0.05). Expression levels of P450scc mRNA in Nano-CdS and CdS groups were (0.50±0.11) and (0.84±0.48),respectively, expression levels of P450-17αmRNA were (0.51±0.13) and (0.72±0.06),respectively. Except P450scc mRNA in CdS group,the mRNA expression levels in experimental groups were significantly lower than control group (P〈0.05). CONCLUSION:Content of cadmium accumulation in testis and sperm deformity rate were increased by exposure to Nano-CdS and CdS,with a significant reduction in serum testosterone levels and expression levels of P450scc and P450-17αmRNA.
Keywords:cadmiumsulfidenano-particles  sperm abnormality  testosterone  cytochrome P450  side-chain cleavage enzyme  steroid 17-alpha-hydroxylase
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