Effects of hypoxia-inducible factor-1α and matrix metalloproteinase-9 on alveolar-capillary barrier disruption and lung edema in rat models of severe acute pancreatitis-associated lung injury

被引:20
|
作者
Qi, Bing [1 ,2 ]
Chen, Hai-Long [2 ]
Shang, Dong [2 ]
Dong, Ying [3 ]
Zhang, Gui-Xin [2 ]
Yu, Lei [1 ]
机构
[1] Dalian Med Univ, Dalian 116044, Liaoning, Peoples R China
[2] Dalian Med Univ, Affiliated Hosp 1, Dept Acute Abdominal Surg, Dalian 116011, Liaoning, Peoples R China
[3] Dalian Med Univ, Affiliated Hosp 2, Dept Gastroenterol & Hepatol, Dalian 116021, Liaoning, Peoples R China
基金
中国国家自然科学基金;
关键词
acute pancreatitis; lung injury; hypoxia-inducible factor-1 alpha; matrix metalloproteinase-9; alveolar-capillary barrier disruption; lung edema; inflammation; UP-REGULATION; EXPRESSION; MIGRATION; ISCHEMIA; GROWTH; LEAK; HIF;
D O I
10.3892/etm.2014.1810
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The aim of this study was to investigate the effects of hypoxia-inducible factor-1 alpha (HIF-1 alpha) and matrix metalloproteinase-9 (MMP-9) on alveolar-capillary barrier disruption and lung edema in rat models of severe acute pancreatitis-associated lung injury (PALI). A total of 40 male Sprague-Dawley rats were randomly divided into a sham surgery group (n=10) and three PALL groups, in which acute pancreatitis was induced by the retrograde infusion of 5% sodium taurocholate (1 ml/kg). The PALI groups were as follows: i) Untreated PALI group (n=10); ii) 2-methoxyestradiol (2ME2) group (5 mg/kg body mass; n=10); and iii) 2ME2 group (15 mg/kg body mass; n=10). In the two 2ME2 groups, the HIF-1 alpha inhibitor 2ME2 was administered intraperitoneally 1 h after the induction of AP. The severity of the pancreatitis was evaluated by the serum amylase levels and pathology: The severity of the lung injury was evaluated by the wet/dry ratio, blood gas analysis and pathology. The alveolar-capillary barrier disruption was assessed by Evans blue dye extravasation. The protein and mRNA expression levels of HIF-1 alpha and MMP-9 were studied using enzyme-linked immunosorbent assays (ELISAs), western blot analysis and reverse transcription-polymerase chain reaction. The active tumor necrosis factor-alpha levels were measured using an ELISA. The HIF-1 alpha inhibitor 2ME2 attenuated the severity of the pancreatitis and PALI, while the lung edema and alveolar-capillary barrier disruption were significantly ameliorated compared with those in the untreated PALI group. Administration of the higher dose of 2ME2 significantly suppressed the protein expression of MMP-9 in the lung tissues. The results indicate that HIF-1 alpha has a major function in alveolar-capillary barrier disruption and lung edema in PALI via a molecular pathway cascade involving MMP-9. Inhibition of HIF-1 alpha by 2ME2 attenuates alveolar-capillary barrier disruption and lung edema. Pharmacological blockade of this pathway in patients with PALI may provide a novel therapeutic strategy.
引用
收藏
页码:899 / 906
页数:8
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