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作 者:王艳[1] 赵凤红[1] 郭连营[1] 钟媛[1] 于霄云[1] 李革新[1] 吕秀强[1] 孙贵范[1] 金亚平[1]
机构地区:[1]中国医科大学公共卫生学院劳动卫生教研室,辽宁沈阳l10001
出 处:《环境与健康杂志》2009年第12期1046-1048,共3页Journal of Environment and Health
基 金:国家自然科学基金资助项目(30571590;30972441);国家自然科学基金重点项目(30530640)
摘 要:目的探讨外源性谷胱甘肽(glutathione,GSH)对饮水砷暴露小鼠脑中砷形态分布及一氧化氮(nitricoxide,NO)代谢的影响。方法将40只雌性昆明小鼠随机分为对照组、单独染砷(NaAsO2)组及低剂量(200mg/kg)、中剂量(400mg/kg)或高剂量(800mg/kg)GSH干预组,每组8只。染毒组小鼠饮水染砷4周,在最后一周,在染砷同时腹腔注射不同剂量GSH。末次注射后24h处死小鼠,取血和脑组织,分别检测无机砷(iAs)、一甲基胂酸(MMA)和二甲基胂酸(DMA)含量及脑中一氧化氮合酶(NOS)活力和NO含量。结果GSH干预组小鼠血中iAs、MMA和总砷(TAs)含量及脑中DMA和TAs含量与单独染砷组比较显著下降。与对照组相比,单独染砷组小鼠脑中NOS活力及NO含量显著降低。与单独染砷组比较,中、高剂量GSH干预组小鼠脑中NOS活力显著升高。结论给予外源性GSH可减少血液和脑组织中的砷负荷,进而改善砷对脑内NO代谢的影响。Objective To explore the effects of exogenous glutathione on arsenic distribution and nitric oxide (NO) metabolism in the brain of mice exposed to arsenite through drinking water. Methods Female Kunming mice were randomly divided into 5 groups, eight in each, and the mice were exposed to sodium arsenite through drinking water at doses of 0 mg/L (control) and 50 mg/L arsenic for 4 consecutive weeks, on the fourth week, with the exposure of arsenic, glutathione was given through intraperitoneal injection at doses of 200 mg/kg b.w, 400 mg/kg b.w or 800 mg/kg b.w, respectively for 7 days. In the end of treatment, the samples of blood and brain were collected. Levels of inorganic arsenic (iAs), monomethylarsonic acid (MMA) and dimethylarsenic acid (DMA) were determined by HG-AAS method. Activities of nitric oxide synthase (NOS) and the concentrations of NO were determined with kits. Results Compared with those in single arsenic group, glutathione significantly decreased levels of iAs, MMA and total arsenic levels (TAs) in the blood and levels of DMA and TAs in the brain. Activities of NOS and levels of NO in As group were significantly lower than those in control, however administration of glutathione could ameliorate these toxic effects, and NOS activities in groups treated with 400 mg/kg b.w and 800 mg/kg b.w glutathionc were significantly higher than those in singlearsenic group. Conclusion Exogenous glutathione may promote methylation of arsenic, therefore reduce arsenic levels in both blood and brain. Moreover, it is proposed that administration of exogenous glutathione can ameliorate the adverse effects of arsenic on NO metabolism in the brain via decreasing the brain arsenic burden.
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