Ischemia and Reperfusion of the Lung Tissues Induced Increase of Lung Permeability and Lung Edema Is Attenuated by Dimethylthiourea (PP69)

被引:6
作者
Chen, K. H. [2 ]
Chao, D. [2 ]
Liu, C. F. [3 ]
Chen, C. F. [4 ]
Wang, D. [1 ]
机构
[1] Fu Jen Catholic Univ, Dept Med, Grad Inst Med, Taipei Hsien, Taiwan
[2] Natl Sun Yat Sen Univ, Dept Biol Sci, Kaohsiung, Taiwan
[3] Natl Taipei Coll Nursing, Taipei, Taiwan
[4] Cheng Hsin Gen Hosp, Dept Internal Med, Div Gastroenterol, Taipei, Taiwan
关键词
INJURY; SUPEROXIDE; INHIBITION; HYPOXIA; RATS; H2O2;
D O I
10.1016/j.transproceed.2010.03.016
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
This study sought to determine whether oxygen radical scavengers of dimethylthiourea (DMTU), superoxide dismutase (SOD), or catalase (CAT) pretreatment attenuated ischemia-reperfusion (I/R)-induced lung injury. After isolation from a Sprague-Dawley rat, the lungs were perfused through the pulmonary artery cannula with rat whole blood diluted 1:1 with a physiological salt solution. An acute lung injury was induced by 10 minutes of hypoxia with 5% CO2-95% N-2 followed by 65 minutes of ischemia and then 65 minutes of reperfusion. I/R significantly increased microvascular permeability as measured by the capillary filtration coefficient (K-fc), lung weight-to-body weight ratio (LW/BW), and protein concentration in bronchoalveolar lavage fluid (PCBAL). DMTU pretreatment significantly attenuated the acute lung injury. The capillary filtration coefficient (P < .01), LW/BW (P < .01) and PCBAL (P < .05) were significantly lower among the DMTU-treated rats than hosts pretreated with SOD or CAT. The possible mechanisms of the protective effect of DMTU in I/R-induced lung injury may relate to the permeability of the agent allowing it to scavenge intracellular hydroxyl radicals. However, whether superoxide dismutase or catalase antioxidants showed protective effects possibly due to their impermeability of the cell membrane not allowing scavenging of intracellular oxygen radicals.
引用
收藏
页码:748 / 750
页数:3
相关论文
共 16 条
  • [1] The role of oxidative stress in adult critical care
    Crimi, E
    Sica, V
    Williams-Ignarro, S
    Zhang, HB
    Slutsky, AS
    Ignarro, LJ
    Napoli, C
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 2006, 40 (03) : 398 - 406
  • [2] Fisher AB, 2004, UNDERSEA HYPERBAR M, V31, P97
  • [3] Hypoxia and reoxygenation increase H2O2 production in rats
    Hitka, P
    Vízek, M
    Wilhelm, J
    [J]. EXPERIMENTAL LUNG RESEARCH, 2003, 29 (08) : 585 - 592
  • [4] N-acetylcysteine attenuates lung ischemia-reperfusion injury after lung transplantation
    Inci, Ilhan
    Zhai, Wei
    Arni, Stephan
    Hillinger, Sven
    Vogt, Peter
    Weder, Walter
    [J]. ANNALS OF THORACIC SURGERY, 2007, 84 (01) : 240 - 246
  • [5] ENDOGENOUS AND EXOGENOUS CATALASE IN REOXYGENATION LUNG INJURY
    JACKSON, RM
    RUSSELL, WJ
    VEAL, CF
    [J]. JOURNAL OF APPLIED PHYSIOLOGY, 1992, 72 (03) : 858 - 864
  • [6] Acute respiratory distress syndrome
    Leaver, Susannah K.
    Evans, Timothy W.
    [J]. BMJ-BRITISH MEDICAL JOURNAL, 2007, 335 (7616): : 389 - 394
  • [7] Hypoxic pulmonary hypertension:: role of superoxide and NADPH oxidase (gp91phox)
    Liu, JQ
    Zelko, IN
    Erbynn, EM
    Sham, JSK
    Folz, RJ
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2006, 290 (01) : L2 - L10
  • [8] XANTHINE-OXIDASE INHIBITION ATTENUATES ISCHEMIC-REPERFUSION LUNG INJURY
    LYNCH, MJ
    GRUM, CM
    GALLAGHER, KP
    BOLLING, SF
    DEEB, GM
    MORGANROTH, ML
    [J]. JOURNAL OF SURGICAL RESEARCH, 1988, 44 (05) : 538 - 544
  • [9] Inflammatory response to pulmonary ischemia-reperfusion injury
    Ng, CSH
    Wan, S
    Arifi, AA
    Yim, APC
    [J]. SURGERY TODAY, 2006, 36 (03) : 205 - 214
  • [10] Catalase delivery for inhibiting ROS-mediated tissue injury and tumor metastasis
    Nishikawa, Makiya
    Hashida, Mitsuru
    Takakura, Yoshinobu
    [J]. ADVANCED DRUG DELIVERY REVIEWS, 2009, 61 (04) : 319 - 326