期刊文献+

乳化氟碳保存液对大鼠供肺的保护作用 被引量:3

Protective effect of perfluorocarbon emulsions on rat donor lung
原文传递
导出
摘要 目的 评价乳化氟碳保存液对大鼠供肺的保护作用.方法 健康雄性SD大鼠24只,体重350 ~ 400 g,采用随机数字表法,将其分为2组(n=12):UW液组(UW组)和乳化氟碳保存液组(FCE组).建立肺灌注模型后取下心肺,置于4℃UW液或乳化氟碳保存液中.于6h时取肺组织,采用WST法测定SOD活性,TBA法测定MDA含量,ELISA法测定MPO活性和IL-1β、IL-6、TNF-α的含量,并观察肺组织病理学结果.结果 与UW组比较,FCE组肺组织MPO活性降低(P<0.05);2组肺组织SOD活性及MDA、IL-1β、IL-6和TNF-α的含量比较差异均无统计学意义(P>0.05).结论 乳化氟碳保存液可降低肺组织中性粒细胞的浸润程度,提示其在减轻供肺损伤方面较UW液更具优势. Objective To evaluate the protective effect of perfluorocarbon emulsions (FCE) on donor lung of rats during storage.Methods Twenty-four healthy male Sprague-Dawley rats,weighing 350-400 g,were equally and randomly divided into 2 groups using a random number table:University of Wisconsin (UW) solution group (UW group) and FCE group (FCE group).After the model of lung perfusion was established according to the method described by Fischer et al,the lung and heart were removed and perfused with 4 ℃ UW or FCE preservation solutions.The lung was taken out when stored for 6 h for determination of SOD activity (by WST assay),malondialdehyde (MDA) content (by TBA assay),and activity of myeloperoxidase (MPO) and content of interleukin1 β (IL-1β),IL-6,tumor necrosis factor-apha (TNF-α) (using ELISA) in lung tissues and for microscopic examination of pathologic changes.Results MPO activity was significantly lower in UW group than in FCE group (P 〈0.05).There were no significant differences in the SOD activity and content of MDA,IL-1β,IL-6,TNF-α between the two groups (P 〉 0.05).Conclusion FCE can reduce the neutrophil infiltration in lung tissues,indicating that FCE is more superior to UW solution in reduction of injury to the donor lung of rats. Keywords:Fluorocarbons ; Emulsifying agents; Lung transplantation; Cytoprotection
出处 《中华麻醉学杂志》 CAS CSCD 北大核心 2013年第9期1082-1084,共3页 Chinese Journal of Anesthesiology
基金 广东省科技计划项目(2010B31600109)
关键词 氟碳化合物 乳化剂 肺移植 细胞保护 Fluorocarbons Emulsifying agents Lung transplantation Cytoprotection
  • 相关文献

参考文献19

  • 1Reznik ON,Bagnenko SF,Loginov IV,et al.The use of oxygenated perfluorocarbonic emulsion for initial in situ kidney perfusion.Transplant Proc,2008,40(4):1027-1028.
  • 2Maillard E,Juszczak MT,Langlois A,et al.Perfluorocarbon emulsions prevent hypoxia of pancreatic β-cells.Cell Transplant,2012,21 (4):657-669.
  • 3Isaka M,Sakuma I,Shiiya N,et al.Experimental study of the relationship between perfluoro-octyl bromide emulsion and norepinephrine release in reperfusion arrhythmia:isolated guinea pig heart model.Ann Thorac Cardiovasc Surg,2008,14(6):363-368.
  • 4Kinasiewicz A,Smietanka A,Gajkowska B,et al.Impact of oxygenation of bioartificial liver using perfluorocarbon emulsion perftoran on metabolism of human hepatoma C3A cells.Artif Cells Blood Substit Immobil Biotechnol,2008,36(6):525-534.
  • 5Fischer S,Hopkinson D,Liu M,et al.Raffinose improves 24-hour lung preservation in low potassium dextran glucose solution:a histologic and ultrastructural analysis.Ann Thorac Surg,2001,71 (4):1140-1145.
  • 6侯萍,李剑平.器官移植前保存的理论研究与临床应用[J].中国组织工程研究与临床康复,2012,16(5):895-898. 被引量:8
  • 7Gale SC,Gorman GD,Copeland JG,et al.Perflubron emulsion prevents PMN activation and improves myocardial functional recovery after cold ischemia and reperfusion.J Surg Res,2007,138(1):135-40.
  • 8何开明,戴天阳.全氟化碳乳剂对肺缺血再灌注损伤的保护机制及其研究进展[J].西南军医,2011,12(6):1078-1080. 被引量:3
  • 9Ma X,Xu D,Ai Y,et al.Fas inhibition attenuates lipopolysaccharide-induced apoptosis and cytokine release of rat type Ⅱ alveolar epithelial cells.Mol Biol Rep,2010,37(7):3051-3056.
  • 10Mason RJ.Biology of alveolar type Ⅱ cells.Respirology,2006,11Suppl:S12-S15.

二级参考文献62

  • 1樊毫军,胡红焱,王海燕,刘书盈,张健鹏,刘又宁.全氟化碳乳剂对急性肺损伤大鼠肺内水通道蛋白1影响的实验研究[J].中华结核和呼吸杂志,2007,30(3):235-236. 被引量:3
  • 2Gunaydin S, Sari T, McCusker K, et al. Clinical evaluation of mini- mized extracorporeal circulation in highrisk coronary revasculariza-tion : impact on air handling,inflammation, hcmodilution and myocar- dial function[ J]. Perfusion ,2009 May ,24 ( 3 ) : 153 - 62. Epub 2009 Sep 15.
  • 3Rudiger M, Wissel H, Ochs M, et al. perfluorocarbons are taken up by isolated typeII pneumocytes and influence its lipid synthesis and secretion[ J]. Crit Care Med ,2003,31 : 1190 - 1196.
  • 4Nakata S, Yasui K, Nakamura T, et al. Perfluorocarbon suppresses li popolysaccharide and alpha - toxin - induced interleukin - 8 release from alveolar epithelial cells[ J]. Neonatology,2007 ,91:127 - 133.
  • 5Obraztov VV ,Neslund GG, Kombrust ES, et al. In vitro cellular effects of perfluorochemicals correlate with their lipid solubility [J]. Am JPhysiol Lung Cell Mol Physiol,2000,278 :L1018- L1024.
  • 6Koch T Ragaller M, Haufe D, et al. Perfluomhexane attenuates pminflammatory and procoagulatory response of activated monocytes and alveolar macrop - hages [ J ]. A nesthesiol ogy, 2001,94 : 101 - 109.
  • 7Dirk H, Luther T, Kotzsch M, et al. Perlluorocarbon attenuates Response of coneanavalin A - stimulated mononuclear blood cells with- out altering ligand - receptor interaction[ J ]. Am J Physiol Lung Cell Mol Physio1,2004 ,287 : L210 - L216.
  • 8EUena JF, Obraztaov VV, Cumbea VL, et o2. Penquoreoetyl bromide has limited membrane solubility and is located at the bilayer center.Locating small molecules in lipid bilayers through paramagnetic en- hancements of NMR relaxation[J]. J Med Chem,2002,45:5534 - 5542.
  • 9Varfolomeev EE, Ashkenazi A. Tumour necrosis factor: an apoptosis Junkie [J]. Ce11,2004-,116(4) :491 -497.
  • 10Fernandez R,Sarma V,Younkin E,et al. Exposure to perflubren is associated with decreased Syk phosphorylation in human neutrophils [J]. J Appl Physiol,2001,91:1941 -1947.

共引文献9

同被引文献14

  • 1Simes EA1, Cardoso PF, PSgo-Femandes PM, et al. An experimen- tal rat model ofex vivo lung perfusion for the assessment of lungs re- garding histopathological findings and apoptosis: low-potassium dextranvs. [J]. J Bras Pneumol, 2012, 38(4): 461-469.
  • 2Okada Y, Kondo T. Preservation solution for lung transplantation [J]. Gen Thorac Carcliovasc Surg, 2009, 57(12): 635-639.
  • 3Kumar V, Sharma A. Adenosine: an endogenous modulator of in- nate immune system with therapeutic potential [J]. Eur J Pharma- col, 2009, 616(1-3): 7-15.
  • 4Fischer S, Hopkinson D, Liu M, et al. Raffinose improves 24-hour lung preservation in low potassium dextran glucose solution: a histo- logic and ultra.structural analysis [J]. Atm-Thorac Surg, 2001, 71(4): 1140-1145.
  • 5Fischer S, Matte-Marty A, de Perrot M, et al. Low-potassium dex-tran preservation solution improves lung function after human lung transplantation [J]. Thorac Cardiovasc Surg, 2001, 121(3): 594-596.
  • 6Witwer T, Franke U, Fehrenbach A, et al. Impact of retrograde graft preservation in perfadex-based experimental lung transplantation [J]. J Surg Res, 2004, 117(2): 239-248.
  • 7De Perrot M, Sekine Y, Fischer S, et al. Interleukiu-8 release dur- ing early reperfusion predicts graft function in human lung trans- plantation [J]. Am J Respir Cfit Care Meal, 2002, 165(2): 211-215.
  • 8彭雪梅,席露,李雅兰,王仲红,王华东.乳化氟碳结合川芎嗪对肝肺综合征猪肝移植围手术期肺部炎症的影响及其机制研究[J].中国病理生理杂志,2010,26(1):112-115. 被引量:5
  • 9WU Rui-ping,LIANG Xiu-bin,GUO Hui,ZHOU Xiao-shuang,ZHAO Li,WANG Chen,LI Rong-shan.Protective effect of low potassium dextran solution on acute kidney injury following acute lung injury induced by oleic acid in piglets[J].Chinese Medical Journal,2012(17):3093-3097. 被引量:7
  • 10龙小毛,林辉,李香伟,周一凡,梁胜景.体外温血持续灌注对猪供肺的保护作用[J].中华实验外科杂志,2012,29(12):2522-2524. 被引量:3

引证文献3

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