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1,1-双(4-氯苯)-2,2,2-三氯乙烷对大鼠神经系统的氧化应激作用

Oxidative Stress of 1,1-Bis(4-chlorophenyl)-2,2,2-trichloro-ethane on Rat Nervous System

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【作者】 梁骏华钟玉芳戴中华石年

【Author】 LIANG Jun-hua,ZHONG Yu-fang,DAI Zhong-hua,SHI Nian*(Department of Public Health and Toxicity,Tongji Medical College,Huazhong University of Science and Technology,MOE Key Lab of Environment and Health, School of Public Health,Tongji Medical College,Huazhong University of Science & Technology,Wuhan 430030,Hubei,China)

【机构】 华中科技大学同济医学院公共卫生学院卫生毒理系华中科技大学同济医学院公共卫生学院卫生毒理系 华中科技大学同济医学院公共卫生学院环境与健康教育部重点实验室湖北武汉430030华中科技大学同济医学院公共卫生学院环境与健康教育部重点实验室

【摘要】 背景与目的:研究1,1-双(4-氯苯)-2,2,2-三氯乙烷(DDT)对大鼠大脑皮层、海马和小脑组织诱导的氧化应激作用。材料与方法:SD大鼠共24只,随机分为4组,即溶剂对照组与低(20mg/kg)、中(40mg/kg)、高(80mg/kg)3个DDT剂量组,每组6只,大鼠经口灌胃染毒7d后断头处死,测定大脑皮层、海马和小脑组织丙二醛(MDA)水平和总超氧化物歧化酶(T-SOD)、谷胱甘肽过氧化物酶(GSH-PX)和谷胱甘肽还原酶(GR)活力。结果:①与溶剂对照组比较,随着DDT浓度的增加,大鼠大脑皮层、海马和小脑中MDA含量升高,T-SOD活性下降;②大脑皮层GSH-PX活性在低剂量时升高,在中、高剂量组则显著下降,海马GSH-PX活性随着剂量的增加而显著下降,而小脑GSH-PX活性则在中、高剂量组出现显著下降;③海马GR活性在中、高剂量组随着剂量的增加而显著下降,在小脑则只有高剂量组出现了下降,皮层GR活性在各剂量组未观察到明显改变。结论:DDT可以引发神经组织的脂质过氧化反应增强。DDT导致机体组织的氧化损伤可能在动物神经毒性中起重要作用。

【Abstract】 BACKGROUND & AIM: To study the oxidative stress induced by 1,1-Bis(4-chlorophenyl)-2,2,2-trichloroethane (DDT) in the cerebral cortex,hippocampus and cerebellum of rats. MATERIAL AND METHODS: 24 Sprague-Dawley male rats were randomly divided into four groups with 6 rats in each: solvent control,low (20 mg/kg),moderate(40 mg/kg) and high(80 mg/kg) dose groups. Test substances were administered by gavage and rats were sacrificed 7 days after treatment. Malonyldialdehyde (MDA),total superoxide dismutase (T-SOD),glutathione peroxidase(GSH-PX) and glutathion reductase (GR) in cerebral cortex,hippocampus and cerebellum were examined .RESULTS: ① Compared with the solvent control, with the dose increased, the content of MDA in cerebral cortex,hippocampus and cerebellum significantly increased while T-SOD activity decreased significantly. ②GSH-PX activity of cerebral cortex significantly increased at low dose group,but significantly decreased at moderate and high dose groups(P<0.05). In hippocampus and cerebellum, with the dose increased ,GSH-PX activity decreased significantly. ③ GR activity of hippocampus decreased significantly at moderate dose and high dose groups(P<0.05). In cerebellum ,it only decreased at high dose group(P<0.05). In cerebral cortex,the alteration of GR activity in different dose groups was not observed. CONCLUSION: DDT could induce oxidative stress in nervous tissue.The tissue oxidative damage might be one of the primary mechanisms of neurotoxicity of DDT.

  • 【文献出处】 癌变.畸变.突变 ,Carcinogenesis,Teratogenesis & Mutagenesis , 编辑部邮箱 ,2006年03期
  • 【分类号】X503.22
  • 【被引频次】1
  • 【下载频次】73
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