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机构地区:[1]黔南民族医学高等专科学校,贵州都匀558003
出 处:《中华综合临床医学杂志(北京)》2005年第10期22-23,共2页chinese journal of composite clinical medicine
摘 要:目的:探讨急性黄磷中毒小鼠血清中一氧化氮(NO)还原型谷胱甘肽(GSH)、丙二醛(MDA)及总抗氧化能力的变化,及其在黄磷中毒发病机制中的作用。方法:通过急性动物实验,小鼠灌胃染毒,分为低、中、高剂量组与对照组,采用生化试剂盒测定各组小鼠血清中NO、GSH、MDA及总抗氧化能力。结果:低剂量组NO、GSH则低于对照组(p〈0.05);各剂量组NO、GSH和总抗氧化能力随染黄磷剂量的增加而降低,MDA水平则显著增高(p〈0.01)。MDA与琥珀酸脱氢酶(SDH)、葡萄糖-6-磷酸酶(G6pD)呈负相关(p〈0.01)。结论:黄磷可引起小鼠血清中GSH、MDA和总抗氧化能力发生变化,进而影响NO合成与代谢.导致脂质过氧化的发生,提示脂质过氧化可能是黄磷中毒的指标之一。Objective:To clarify the variety and the significanc of nitric oxide(NO), glutathione(GSH), maleic dialdehyde(MDA) and total anti-oxidize ability in serum poisoning, Methods: Animal experiment and biochemistry agent box of NO, GSH, MDA and total anti-oxidize ability were used.Results: The contents of NO and GSH in low dose groups were higher than those in controls serum of mice(P〈0.05), and decreased in high dose group.NO, GSH and total anti-oxidze ability in all experimental groups decreased and slowed a dose-effect manner. MDA in all groups increased significantly and showed a dose-effect manner (p〈0.01). The MDA was negatively correlationed with sorbic dehydgenase and glucose-6-phosphate dehydgenase(p〈0.01). Conclusion: The changes of GSH, MDA and total anti-oxidize ability could be affected by yellow phosphorus. The synthesis or metabolize of NO may be correlated with the influence of yellow phosphorus on GSH, MDA and total anti-oxidize ability. The results induce lipid peroxidation (LPO) in mice, LPO might be one of the mechanism of yellow phosphorus poisoning.
关 键 词:黄磷 一氧化氮 谷胱甘肽 丙二醛 脂质过氧化 丙二醛(MDA) 总抗氧化能力 急性动物实验 黄磷中毒 小鼠血清
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