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硫化氢对大鼠肺缺血再灌注氧化损伤的影响 被引量:8

Impact of hydrogen sulfide on oxidative damage in lung of rats after ischemia-reperfusion
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摘要 目的探讨硫化氢对大鼠肺缺血再灌注氧化损伤的影响。方法以硫化氢钠(NaHS)作为硫化氢供体。50只健康SD大鼠,随机分成假手术组、肺缺血再灌注组及硫氢化钠(NaHS)组,后者进一步分为NaHS10、20、30μmol.kg-13个剂量组;每组10只。NaHS组实验前5d开始每天按体重分别腹腔注射不同剂量的NaHS,实验前15min再次给药;假手术组和肺缺血再灌注组同时同方法给予生理盐水1ml.kg-1。建立大鼠在体肺缺血再灌注模型,实验结束时左心房放血处死大鼠,观察肺组织病理改变,测定肺湿/干重(W/D)值及肺组织匀浆内丙二醛(MDA)、髓过氧化物酶(MPO)含量及超氧化物岐化酶(SOD)、谷胱甘肽过氧化物酶(GSH-Px)活性。结果肺缺血再灌注组肺组织W/D值、MDA、MPO水平均较假手术组明显升高(P<0.01),而NaHS组上述指标高于假手术组但低于肺缺血再灌注组(均P<0.05);肺缺血再灌注组肺组织SOD、GSH-Px活性较假手术组明显降低(P<0.01),NaHS组上述指标低于假手术组但明显高于肺缺血再灌注组(P<0.05或P<0.01)。上述指标在NaHS3个剂量组间的差异无统计学意义。肺组织病理学检查结果显示,NaHS组肺缺血再灌注损伤减轻。结论硫化氢具有一定的抗大鼠肺缺血再灌注氧化损伤的能力,其作用机制与清除氧自由基及增加内源性抗氧化酶活性有关。 Objective To explore the impact of hydrogen sulfide(H2S) on oxidative damage in lung of rats after ischemia-reperfusion.Methods We used sodium hydrosulfide(NaHS) as the donor of H2S.Fifty SD rats were randomly divided into sham group(n=10),lung ischemia-reperfusion group(IR group,n=10) and IR+NaHS group,and the IR+NaHS group was divided into IR+NaHS 10μmol·kg-1 group(n=10),IR+NaHS 20 μmol·kg-1 group(n=10),IR+NaHS 30μmol·kg-1 group(n=10).Five days before the experiment,rats of IR+NaHS(10μmol·kg-1,20μmol·kg-1and 30μmol·kg-1) groups were pretreated(intraperitoneal injection) with different dose of NaHS according to the weight,and administration again 15 min before the experiment;sham group and IR group were pretreated(intraperitoneal injection) with normal saline(1ml·kg-1).An rat lung I/R model was built in vivo.At the end of the experiment,all rats were put to death after blood was collected from left atrium.We examined indices of lung injury:lung histological change,ratio of lung wet weight to dry weight (W/D),malondialdehyde(MDA) and myeloperoxidase(MPO) content,activities of superoxide dismutase(SOD) and glutathione peroxidase(GSH-Px) in lung tissues.Results The W/D ratio of lung tissue,contents of MDA and MPO in lung tissue in the IR group and IR+NaHS groups were significantly higher than those in the sham group (P〈0.05 or P〈0.01),while the indices above in IR+NaHS groups were significantly lower than those in the IR group(P〈0.05);The activities of SOD and GSH-Px in lung tissue in the IR group and IR+NaHS groups were significantly lower than those in the sham group (P〈0.05 or P〈0.01),while the indices above in IR+NaHS groups were significantly higher than those in the IR group(P〈0.05 or P〈0.01).All the indices abovementioned had no statistical significance in three dose of IR+NaHS groups.The lung histological change also showed that pre-administration of NaHS could relieve lung ischemia-reperfusion injury.Conclusions These findings suggest that H2S has a certain ability of anti-oxidative damage in lung of rats after ischemia-reperfusion.Its mechanism involves oxyradical elimination and increase the endogenous antioxidant enzyme activity.
出处 《现代医学》 2009年第3期184-188,共5页 Modern Medical Journal
关键词 肺缺血再灌注损伤 硫化氢 硫氢化钠 氧自由基 氧化损伤 lung ischemia reperfusion injury hydrogen sulfide sodium hydrosulfide oxygen free radical oxidative damage
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  • 1Chavez-Cartaya R,Jamieson N V, Ramirez P,et al. Free radical scavengers to prevent reperfusion injury followings experimental warm liver ischemia[ J ]. Transpl Int, 1999,12 (3) :213-221.
  • 2Novick R J, Gehman K E, Ali I S, et al. Lung preservation:the importance of endothelial and alveolar type Ⅱ cell integrity[J]. Ann Thorac Surg, 1996,62( 1 ) :302.
  • 3Zhang X, Bedard E L, Potter R, et al. Mitogen-activated protein kinases regulate HO-1 gene transcription after ischemia-reper- fusion lung injury [ J ]. Am J Physiol Lung Cell Mol Physiol, 2002,283 (4):L815-829.
  • 4Wang R. Two's c ompany,three's a crowd:can HES be the third endogenous gaseous transmitter? [ J ]. FASEB J, 2002, 16 (13) :1792-1798.
  • 5Chen Y H,Yao W Z, Geng B, et al. Endogenous hydrogen sulfide in patients with COPD [ J ]. Chest, 2005, 128 (5), 3205-3211.
  • 6Zhang H, Zhi L, Moore P K, et al. Role of hydrogen sulfide in cecal ligation and puncture-induced sepsis in the mouse [ J], Am J Physiol Lung Cell Mol Physiol, 2006,290 ( 6 ), L1193- L1201.
  • 7Li H, Liu X M, Geng B, et al. Effect of hydrogen sulfide on bleomycin-induced pulmonary fibrosis in rats [ J ]. Beijing Da Xue Xue Bao, 2006,38 ( 2 ) , 140 - 145.
  • 8Ruiz-Gines J A, Lepez-Ongil S,Gonzdlez-Rubio M,et al. Reactive oxygen species induce proliferation of bovine aortic endothelial cells [ J ]. J Cardiovasc Pharmacol, 2000, 35 ( 1 ) : 109-113.
  • 9Linder N, Rapola J, Raivio K O. Cellular expression of xanthine oxidoreductase protein in normal human tissue[ J]. Lab Invest, 1999,79 ( 8 ) :967-974.
  • 10Fu Z, Liu X, Geng B, et al. Hydrogen sulfide protects rat lung from ischemia-reperfusion injury [ J ]. Life Sciences, 2008 ( 23- 24), 82 : 1196-1202.

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