The effect of enoxaparin on bleomycin-induced lung injury in mice

被引:1
作者
Laxer, U
Lossos, IS
Gillis, S
Or, R
Christensen, TG
Goldstein, RH
Breuer, R
机构
[1] Hadassah Univ Hosp, Inst Pulm, Lung Cellular & Mol Biol Lab, IL-91120 Jerusalem, Israel
[2] Hebrew Univ Jerusalem, Hadassah Med Sch, IL-91010 Jerusalem, Israel
[3] Hadassah Univ Hosp, Dept Hematol, IL-91120 Jerusalem, Israel
[4] Hadassah Univ Hosp, Dept Bone Marrow Transplantat, IL-91120 Jerusalem, Israel
[5] Boston Univ, Sch Med, Dept Pathol, Mallory Inst Pathol, Boston, MA 02118 USA
[6] Boston Univ, Sch Med, Ctr Pulm, Boston, MA 02118 USA
关键词
bleomycin; enoxaparin; interstitial lung disease; low-molecular-weight heparin; mice;
D O I
暂无
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
We have evaluated the effect of enoxaparin, a potent antithrombotic drag, on bleomycin (Bleo)-induced pulmonary inflammation in mice. Pulmonary injury was induced by a single intratracheal (IT) instillation of Bleo. Four groups of female C57BL/6 mice, each received one of four treatments: (1) IT Bleo and daily intraperitoneal (IP) injections of enoxaparin (EN) starting one day before IT instillation of Bleo (Bleo-EN); (2) IT Bleo and IP injections of saline (Bleo-Sal); (3) IT saline and IP enoxaparin (Sal-EN); (4) IT saline and IP saline (Sal-Sal). Animals were sacrificed 14 days after IT treatment. Lung injury was evaluated by analysis of bronchoalveolar lavage fluid and histologically by an overall semiquantitative index of lung injury and a quantitative image analysis assessing alveolar mall area fraction and fibrosis fraction. Treatment of nice with enoxaparin did not ameliorate Bleo-induced lung injury. Our study does not establish a critical role of procoagulant activity in the evolution of Bleo-induced lung injury and does not support the use of antithrombotic therapy for the prevention of pulmonary fibrosis.
引用
收藏
页码:531 / 541
页数:11
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