期刊文献+

吲哚硒对小鼠化学性肝损伤的保护作用 被引量:9

Protective effects of indole-selenium of indole selenium on chemical liver injury induced in mice
暂未订购
导出
摘要 目的 探讨吲哚硒对四氯化碳 (CCl4)致小鼠急性化学性肝损伤的保护作用及可能机制。方法 建立CCl4诱导小鼠化学性肝损伤模型 ,分光光度法检测血浆中ALT、AST水平和肝匀浆MDA、SOD、GSH Px含量 ,HE染色法对肝脏组织作病理检查。结果 吲哚硒 (5、10、2 0mg/kg)灌胃给药均能降低血浆中升高的转氨酶水平 ,病理检查也发现其可明显减轻肝组织坏死范围及程度 ,减少炎细胞浸润。同时发现吲哚硒可降低肝匀浆中升高的MDA水平 ,使降低的肝匀浆SOD、GSH Px酶活性升高。结论 吲哚硒对CCl4致小鼠急性化学性肝损伤具有保护作用 ,其机制与其抗自由基、提高抗氧化物酶的活性等有关。 Objective To investigate the effects of indole-selenium on carbon tetrachloride-induced liver injury. Methods The model of mice chemical liver injury was prepared.The level of alanine aminotransferase(ALT), aspartate aminotransferase(AST) in plasma, malondiadehyde(MDA) content, superoxide dismutase(SOD) and glutathione peroxidase(GSH-Px) activities in liver homogenate were assayed by spectrophotometer; Hepatic pathological examination was observed. Results Indole-selenium (5,10,20 mg/kg) was able to significantly decrease serum transaminase (ALT,AST) levels, attenuate the area and extent of necrosis and reduce the infiltration of inflammatory cells. Furthermore, indole-selenium also decreased MDA content and improved the reduced SOD and GSH-Px level in liver homogenate. Conclusion Indole-selenium possesses protective action on chemical liver injury in mice.
出处 《安徽医科大学学报》 CAS 2003年第3期179-182,共4页 Acta Universitatis Medicinalis Anhui
基金 安徽省教育厅重点科研基金资助 (编号 :98JL0 13 0Z)
关键词 吲哚硒 小鼠 化学性肝损伤 保护作用 分光光度法 检测 HE染色法 病理学 melatonin/pharmacology selenium/pharmacology liver diseases/pathology
  • 相关文献

参考文献10

  • 1郭利,恽榴红.含硒化合物研究进展[J].中国新药杂志,2000,9(3):155-158. 被引量:25
  • 2王华,沈玉先,魏伟,周爱武,张玲玲,岳莉,徐叔云.鸡Ⅱ型胶原对小鼠胶原性关节炎的治疗作用[J].中国药理学通报,2002,18(1):76-78. 被引量:7
  • 3Xueyun Gao,Jinsong Zhang, Lide Zhang. Hollow sphere selenium nanoparticles:their invitro anti hydroxyl radical effect. Adv Mater, 2002;14(4) :290-3.
  • 4Calvo JR, Reiter RJ, Garcia JJ et at. Characterization of the protective effects of melatonin and related indoles against alphanaphthylisothiocyanate-induced liver injury in rats. J Cell Biochem. 2001;80(4): 461-70.
  • 5Melchiorri D, Reiter RJ, Attia AM et al. Potent protective effect of melatonin on in vivo paraquat-induced oxidative damage in rats. Life Sci, 1995; 56(2):83-9.
  • 6Sewerynek E, Reiter RJ, Melchiorri D et al. Oxidative damage in the liver induced by ischemia-reperfusion., protection by melatonin. Hepato-Gastroenterol, 1996;43(10):898-905.
  • 7Ohta Y, Kongo M, Sasaki E et al. Therapeutic effect of melatonin on carbon tetrachloride-induced acute liver injury in rats.J Pineal Res. 2000;28(2) :119-26.
  • 8Recknagel RO,Glende EA, Dolak JA et at. Mechanisms of carbon tetrachloride toxicity. Pharmac Ther,1989,43(5) :139-54.
  • 9Muller A, Cadenas E, Graf Pet al. A novel biologically active seleno-organic compound-I. Glutathione peroxidase-like activity in vitro and antioxidant capacity of PZ51(Ebselen). Biochem Pharmacol, 1984;33(24) :3235-46.
  • 10Stasica P, Ulanski P, Rosiak JM. Melatonin as a hydroxyl radical scavenger. J Pineal Res, 1998;25(1):65-6.

二级参考文献19

  • 1梁君山,魏伟,周爱武,陈敏珠,徐叔云.白细胞介素Ⅰ的检测及白芍总甙对其产生的影响[J].中国药理学通报,1989,5(6):354-357. 被引量:51
  • 21,Gregus Z, Perjesi P,Gyurasics A. Enhancement of selenium excretion in bile by sulfobromophthalein: elucidationof the mechanism. Biochem Pharmacol, 1998, 56(10)∶1391
  • 32,Behne D, Kyriakopoeulos A, Weiss-Nowak C, et al. Newly found selenium-containingproteins in the tissues of the rat. Biol Trace Elem Res, 1996, 55(1/2)∶99
  • 43,Behne D, Hammel C, Pfeifer H, et al. Speciation of selenium in the mammalian organism.Analyst, 1998, 123(5)∶871
  • 54,May SW, Pollock SH. Selenium-based antihypertensives. Rationale and potential. Drugs,1998, 56(6)∶959
  • 65,May SW, Wang LQ, Giu-Woznichak MM, et al. An orally active selenium basedantihypertensive agent with restricted CNS permeability. J Pharmacol Exper Ther, 1997,283(2)∶470
  • 76,Jacob C, Maret W, Vallee BL. Ebselen, a selenium-containing redox drug, releases zincfrom metallothionein. Biochem Biophys Res Commun, 1998, 248(3)∶569
  • 87,Kondo H, Takahashi M, Niki E. Peroxynitrite-induced hemolysis of human erythrocytesand its inhibition by antioxidants. FEBS Lett, 1997, 413(2)∶236
  • 98,Roussyn I, Briviba K, Masumoto H, et al. Selenium-containing compounds protect DNAfrom single-strand breaks caused by peroxynitrite. Arch Biochem Biophys,1996, 330(1)∶216
  • 109,Sies H, Sharov VS, Kiotz LO, et al. Glutathione peroxidase protects againstperoxynitrite-mediated oxidations. J Biol Chem, 1997, 272(44)∶27812

共引文献29

同被引文献67

引证文献9

二级引证文献34

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