题名 | Effects of COX-2 inhibitor on ventilator-induced lung injury in rats |
作者 | |
发表日期 | 2013-06 |
发表期刊 | INTERNATIONAL IMMUNOPHARMACOLOGY 影响因子和分区 |
语种 | 英语 |
原始文献类型 | Article |
关键词 | Mechanical ventilation Lung injury Aquaporin Cyclooxygenase inhibitors |
其他关键词 | NECROSIS-FACTOR-ALPHA ; NF-KAPPA-B ; ISOLATED MOUSE LUNGS ; MECHANICAL VENTILATION ; EPITHELIAL-CELLS ; DOWN-REGULATION ; MESSENGER-RNA ; AQUAPORIN-3 EXPRESSION ; ACUTE-PANCREATITIS ; PULMONARY-EDEMA |
摘要 | Background: Mechanical ventilation especially with large tidal volume has been demonstrated to activate inflammatory response inducing lung injury, which could be attenuated by cyclooxygenase (COX)-2 inhibitors. As the main small integral membrane proteins that selectively conduct water molecules' transportation, aquaporin (AQP)-1 downregulation significantly related to lung edema and inflammation. This study aims to investigate the role of AQP1 in ventilator-induced lung injury in rats and evaluates the effects of COX-2 inhibition. Methods: Forty rats were allocated into four groups, where rats in Groups LD (low volume + DMSO) and LN (low volume + NS-398) were given intravenously 2 ml DMSO and 8 mg/kg NS-398 (a specific COX-2 inhibitor, dissolved in 2 ml DMSO) before 4-hour lower tidal volume ventilation (8 ml/kg), respectively, while DMSO and NS-398 were administrated in the same manner before 4-hour injurious ventilation (40 ml/kg) in Groups HD (high volume + DMSO) and HN (high volume + NS-398). The arachidonic acid metabolites (6-keto prostaglandin F1 alpha, thromboxane B-2), inflammatory cytokines (tumor necrosis factor-at, interleukin-1 beta, 6,8) and total protein levels in bronchoalveolar lavage (BAL) fluid and COX-2 mRNA and AQP1 protein expression in lung tissue were detected; water content and lung morphology were also evaluated. Results: Compared to Groups LD and LN, the rats in Groups HD and HN suffered obvious lung morphological changes with higher wet-to-dry weight ratio and lung injury score, and the levels of arachidonic acid metabolites, inflammatory cytokines and total protein in BAL fluid were increased, the expression of COX-2 mRNA was significantly upregulated and AQP1 protein was downregulated in lung tissue (p < 0.05). The changes in BAL fluid and the severity of lung injury were attenuated, and AQP1 expression was upregulated in Group HN as compared to HD (p < 0.05). Conclusions: Ventilation with large tidal volume causes inflammatory mediator production and AQP1 downregulation, which could be attenuated by COX-2 inhibition. (c) 2013 Elsevier B.V. All rights reserved. |
资助项目 | Science and Technology Bureau of Wenzhou City, Zhejiang Province, China [Y20100025] |
出版者 | ELSEVIER SCIENCE BV |
出版地 | AMSTERDAM |
ISSN | 1567-5769 |
EISSN | 1878-1705 |
卷号 | 16期号:2页码:288-295 |
DOI | 10.1016/j.intimp.2013.03.031 |
页数 | 8 |
WOS类目 | Immunology ; Pharmacology & Pharmacy |
WOS研究方向 | Immunology ; Pharmacology & Pharmacy |
WOS记录号 | WOS:000320895400024 |
收录类别 | SCIE ; PUBMED |
URL | 查看原文 |
PubMed ID | 23587488 |
通讯作者地址 | [Lin, Li-na]Wenzhou Med Coll, Affiliated Hosp 1, Dept Anesthesiol, Wenzhou 325000, Zhejiang, Peoples R China. |
TOP期刊 | TOP期刊 |
引用统计 | |
文献类型 | 期刊论文 |
条目标识符 | https://kms.wmu.edu.cn/handle/3ETUA0LF/12736 |
专题 | 附属第一医院 附属第二医院 附属第二医院_呼吸内科 附属第一医院_麻醉科 第二临床医学院、附属第二医院、育英儿童医院 |
通讯作者 | Lin, Li-na |
作者单位 | 1.Wenzhou Med Coll, Affiliated Hosp 1, Dept Anesthesiol, Wenzhou 325000, Zhejiang, Peoples R China; 2.Wenzhou Med Coll, Affiliated Hosp 2, Dept Resp Med, Wenzhou, Peoples R China |
第一作者单位 | 附属第一医院; 麻醉科 |
通讯作者单位 | 附属第一医院; 麻醉科 |
第一作者的第一单位 | 附属第一医院 |
推荐引用方式 GB/T 7714 | Jin, Li-da,Wang, Liang-rong,Wu, Li-qin,et al. Effects of COX-2 inhibitor on ventilator-induced lung injury in rats[J]. INTERNATIONAL IMMUNOPHARMACOLOGY,2013,16(2):288-295. |
APA | Jin, Li-da., Wang, Liang-rong., Wu, Li-qin., Shan, Yuan-lu., Zhao, Xi-yue., ... & Jin, Lie-lie. (2013). Effects of COX-2 inhibitor on ventilator-induced lung injury in rats. INTERNATIONAL IMMUNOPHARMACOLOGY, 16(2), 288-295. |
MLA | Jin, Li-da,et al."Effects of COX-2 inhibitor on ventilator-induced lung injury in rats".INTERNATIONAL IMMUNOPHARMACOLOGY 16.2(2013):288-295. |
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