期刊文献+

急性砷中毒小鼠血清中NO、GSH、MDA及总抗氧化能力的实验研究 被引量:14

Experimental study on nitric oxide, glutathione, maleic dialdehyde and total anti-oxidize ability in serum of mice with acute arsenic poisoning
下载PDF
导出
摘要 目的探讨急性砷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,及其在砷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、高剂量组及对照组,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。结果低剂量组小鼠血清中NO、GSH显著高于对照组(P<0.05),高剂量组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砷剂量的增加而降低,MDA水平则显著增高(P<0.01)。结论三氧化二砷(As2O3)可引起小鼠血清中GSH、MDA和总抗氧化能力发生改变,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砷中毒的机理之一。 Objective To clarify the variety and the significance of nitric oxide(NO), glutathione(GSH), maleic dialdehyde(MDA) and total anti-oxidize ability in serum of mice with acute arsenic 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 in serum of mice(P < 0.05), and decreased in high dose group. NO, GSH and total anti-oxidize ability in all experimental groups decreased and showed a dose-effect manner. MDA in all groups increased significantly and showed a dose-effect manner(P < 0.01). Conclusions The changes of GSH, MDA and total anti-oxidize ability could be affected by As2O3. The synthesis or metabolize of NO may be correlated with the influence of arsenite on GSH, MDA and total anti-oxidize ability. The results indicates that arsenic could induce lipid peroxidation (LPO) in mice. LPO might be one of the mechanism of arsenic poisoning.
出处 《中国地方病学杂志》 CAS CSCD 北大核心 2004年第4期325-326,共2页 Chinese Jouranl of Endemiology
关键词 急性砷中毒 小鼠 血清 NO GSH MDA 总抗氧化能力 实验 一氧化氮 还原型谷胱甘肽 丙二醛 Arsenic Nitric oxide Glutathione Maleic dialdehyde Lipid peroxidation
  • 相关文献

参考文献4

二级参考文献59

  • 1李建学 张研 等.地方性砷中毒患者血中氧自由基代谢的变化.第三届全国地方病学术会议论文集[M].,1996.205.
  • 2Hyun DH,Lee M, Hattori N, et al. Effect of wild- type or mutant parkin on oxidative damage, nitric oxide, antioxidant defenses, and the proteasome [J].J Bid Chem, 2002; 277(32) : 28572.
  • 3Wiesinger H. Arginine metabolism and the synthesis of nitric oxidein the nervous system[J]. Prog Neurobiol, 2001; 64(4) : 365.
  • 4Doboszynska T, Andronowska A, Moclzelewska B. Immunohistochemical localization of ET - 1 and eNOS inlymphatic stomata of the porcine broad ligament of the uterus[J]. Folia Histochem Cytobiol, 2001; 39:15.
  • 5Ye JS, Tipoe GL, Fung PC, et al. Augmentation of hypoxia- induced nitric oxide generation in the rat carotid body adapted to chronic hypoxia: an involvement ofconstitutive and inducible nitric oxide synthases[ J ]. Pflugers Arch, 2002; 444 (1 -2) : 178
  • 6Nightingale AK, Bhchnan DJ, Field R, et al.The role of nitric oxide and oxid - afire stress in baroreceptor dysfunction in patients with chronic heart failure[J]. Clin Sci, 2003, 28;[epub ahead of print].
  • 7Peng X, Haldar S, Deshpande S, et al. Wall stiffness suppresses Akt/eNOS and cytoprotection in pulse- perfused endothelium[J]. Hypertension, 2003; 41 (2): 378.
  • 8Miyamoto T, Takeishi Y, Shishido T, et al. Role of nitric oxide in the progression of cardiovascular remodeling induced by carotid artexio - cenous shunt inrabbits[ J ]. Jpn Heart J,2003; 44 (1): 127.
  • 9Morbidelli L, Donnini S, Ziche M. Role of nitric oxide in the modulation of ang- iogenesis[ J ]. Curr Pharm Des,2003; 9 (7): 521.
  • 10Mizushima H, ghou C.j, Dohi K, et at. Reduced postischemic apoptosis in the hippocampus of mice deficient in intedeukin-1[J]. J Comp Neurol, 2002; 448 (2): 203.

共引文献46

同被引文献223

引证文献14

二级引证文献50

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部