期刊文献+

快速减压后大鼠肺组织自由基含量的变化 被引量:3

Alteration of Free Radical Generation in Pulmonary Tissue after Quick Decompression
暂未订购
导出
摘要 采用EPR波谱仪测定肺组织内自由基变化以评价快速减压对肺的损伤。把SD大鼠在0.5MPa空气中暴露60min,用1min匀速减至常压,然后分别在45min和90min时腹腔放血处死(处死前25min注入0.05M的PBN,0.5ml/100g),取肺0.75g匀浆后用EPR波谱仪测定维生素C自由基(Vc)强度。结果显示减压后45min肺组织内Vc强度无明显变化,减压90min组的肺组织内Vc强度明显增高(P<0.05)。表明快速减压可引起肺组织自由基增加。 The purpose of this experirment was to evaluate decompression-induced pulmonary injury by means of measurement of ascorbate free radical (Vc) alteration in pulmonary tissue of the rats which experienced rapid decompression. 29 male S-D rats were divided into 4 groups: A was executed at 45 min post-decompression; B was control for A; C was executed at 90 min;D was ontrol for C. Group A and group C were to compress up to 0. 5 MPa(air) and stay for 60 min, then were decompressed smoothly to normbaric in 1 min. The 0.05M N-tert-butylalpha-phenylnitrone (PBN) was given at 20 min after completion of decompression (groups A and B) or at 65 min (groups C and D). At 25 min after PBN injection the animals were killed by cutting arteria coeliaca, and 0. 75 g pulmonary tissues were taken. These tissues were homogenized for electron paramagnetic resonance (EPR) assay.The results demonstrated that the ascorbate free radical (Vc) signals were obtained at all samples. The intensity of signals measured in group C rose markedly (P<0.05) and that in group A was close to control's. So it can be concluded that rapid decompression would increase the generation of free radical in lung.
出处 《生物医学工程学杂志》 EI CAS CSCD 北大核心 2000年第2期238-240,共3页 Journal of Biomedical Engineering
关键词 快速减压 维生素C 自由基 肺组织 大鼠 Quick decompression Ascorbic acid Free radical Lung
  • 相关文献

参考文献1

共引文献2

同被引文献33

  • 1刘珊林,施冬云,姚诗凯,于大江.大鼠及兔抗氧自由基的代偿效应观察[J].上海第二医科大学学报,1996,16(3):201-203. 被引量:5
  • 2倪大智 姜德玺 等.高压氧暴露大鼠肺内自由基生成变化.高压氧医学的理论与新技术[M].北京:军事医学科学出版社,1998.11-16.
  • 3Krinsky NI. Antioxidant functions of carotenoids[J]. Free Radic Biol Med, 1989,7(6):617.
  • 4Bitterman N, Mclamed Y, Ben Amotz A. β-carotene and CNS toxicity in rats[J]. JAppl Physiol, 1994, 76:1073-1076.
  • 5Ernster L, Dallner G. Biochemical, physiological and medical aspects of ubiquinonefunction[J]. Biochim Biophys Acta, 1995, 1271(1):195.
  • 6Feri B, Ames BN. What is the most important antioxidant in human extracellularfluids? Antioxidants and biochemistry-symposium #200 satellite meeting of oxygen societyand the international society for free radical research. University of Califorma, 1990.41.
  • 7Rose RC, Bode AM. Biology of free radical scavenger: an evaluation ofascorbate[J]. FASEB J, 1993, 7:1135-1142.
  • 8McCay PB, Biological systems which suppress lipid peroxidation. In: Singal PK ed.Oxygen radicals in the pathophysiology of heart disease[J]. Boston: Kluwer AcademicPublishers, 1988. 13-27.
  • 9Van Klaveren RJ, Demedts M, Nemery B. Cellular glutathione turnover in vitro, withemphasis on type Ⅱ pneumocytes[J]. Eur Respir J, 1997, 10(6):1392-1400.
  • 10Boldyrev AA. Does carnosine possess direct antioxidat activity[J]? Int J Biochem,1993, 25(8):1101-1107.

引证文献3

二级引证文献2

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