李蓉,冷言冰,艾国平,等.长期食入低剂量贫铀对大鼠的生殖毒性研究[J].中华放射医学与防护杂志,2007,27(5):417-420.LI Rong,LENG Yan-bing,AI Guo-ping,et al.Reproductive toxicity in rats after chronic oral exposure to low dose of depleted uranium[J].Chin J Radiol Med Prot,2007,27(5):417-420
长期食入低剂量贫铀对大鼠的生殖毒性研究
Reproductive toxicity in rats after chronic oral exposure to low dose of depleted uranium
投稿时间:2006-10-09  
DOI:
中文关键词:  贫铀  低剂量  生殖毒性  食入
英文关键词:Depleted uranium  Low dose  Reproductive toxicity  Intake
基金项目:国家自然科学基金资助项目(30670625);全军“十一五”科研基金专项项目(06Z031);中国博士后基金(2006039068)
作者单位E-mail
李蓉 400038 重庆, 第三军医大学军事预防医学院复合伤研究所创伤烧伤复合伤国家重点实验室  
冷言冰 成都医学院公共卫生学教研室  
艾国平 400038 重庆, 第三军医大学军事预防医学院复合伤研究所创伤烧伤复合伤国家重点实验室  
徐辉 400038 重庆, 第三军医大学军事预防医学院复合伤研究所创伤烧伤复合伤国家重点实验室  
粟永萍 400038 重庆, 第三军医大学军事预防医学院复合伤研究所创伤烧伤复合伤国家重点实验室 Suyping@yahoo.com 
程天民 400038 重庆, 第三军医大学军事预防医学院复合伤研究所创伤烧伤复合伤国家重点实验室  
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中文摘要:
      目的 研究长期食入低剂量贫铀对大鼠的生殖毒性。方法 给予初断乳大鼠含贫铀饲料,食入贫铀的剂量分别为0、0.4、4和40 mg·kg-1·d-1,4个月后,采用两代一窝法观察整体生殖毒性效应;放射免疫法检测睾酮(T)、黄体生成素(LH)、卵泡刺激素(FSH)等血清性激素水平;比色法测定睾丸中乳酸脱氢酶同工酶(LDH-X)、琥珀酸脱氢酶(SDH)及Na+-K+-ATPase、Ca2+-ATPase等精子生成和代谢有关酶的比活性。结果 亲代(F0代)大鼠各项指标未见显著改变。子代(F1代)高剂量组的受孕率、正常分娩存活率、幼仔出生存活率、幼仔哺育存活率均下降,与对照组相比,差异有统计学意义。食入贫铀的F0代大鼠血清性激素含量较正常组增加,但F1代除T升高外,其余性激素均下降。F0代高剂量组睾丸中LDH含量降低;F1代大鼠中、高剂量组SDH、LDH和Na+-K+-ATPase含量降低。结论 长期食入低剂量的贫铀对F0代大鼠未见明显生殖毒性,但F1代大鼠的生殖毒性效应显著增加。
英文摘要:
      Objective To study the reproductive toxicity in rats induced by low dose of depleted uranium (DU). Methods Male and female rats(F0 generation) were exposed to DU in food at doses of 0, 0.4, 4and 40 mg·kg-1·d-1 for 160 days,respectively. Then the activities of enzymes in testis and sexual hormone contents in serum were detected. Mature male rats were mated with female rats exposed to the same doses for 14 days. Pregnant rate and normal labor rate in F0 rats were detected, as well as the survival rate and weight of F1 rats within 21 d after birth. Results No adverse effects of DU on fertility were evident at any dose in F0 rats. Compared with control group, the rate of pregnancy, normal labor, survival of offspring birth and offspring nurture in F1 generation of high_dose group reduced to 40.0%, 33.3%, 33.3%, and 33.3%, respectively. The sexual hormone contents in F0 generation exposed increased, but those in F1 rats decreased significantly. The activities of lactate dehydrogenase-X (LDH-X) decreased in F0 rats exposed to high-dose of DU, and those of sorbitol dehydrogenase (SDH), LDH and Na+-K+-ATPase decreased in F1 rats exposed to DU. Conclusions Reproduction function, growth and development of F0 rats are not obviously affected after chronic oral exposure to DU, while the toxicity effects in F1 generation was observed at any dose.
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