罗格列酮通过降低IL-17减轻LPS诱导的新生大鼠急性肺损伤

被引:5
作者
罗艳
李清香
杨洁
雷贤明
曹云涛
机构
[1] 遵义医科大学附属医院新生儿科
关键词
肺损伤; 脂多糖; SD新生大鼠;
D O I
暂无
中图分类号
R965 [实验药理学];
学科分类号
100706 [药理学];
摘要
目的探讨罗格列酮(rosiglitazone,RGZ)对脂多糖(lipopolysaccharide LPS)诱导的新生大鼠急性肺损伤气道炎症的影响及其机制。方法清洁级SD新生大鼠随机分为对照组、LPS组及罗格列酮干预组。LPS组鼻腔中滴入LPS的剂量为4 mg/kg,对照组给予等量生理盐水,罗格列酮干预组鼻腔中滴入LPS(剂量同前)1 h后腹腔内注射罗格列酮(2 mg/kg);对照组和LPS组鼻腔滴入等量LPS或生理盐水1 h后腹腔注射等量生理盐水。各组新生鼠分别于6、12、24 h被处死,然后评估肺组织的病理评分、湿/干质量比值(W/D)、支气管肺泡灌洗液(BALF)中多形核白细胞(PMN)计数,并检测BALF中的IL-17水平。结果与对照组相比,不同时间点LPS组的肺组织炎症病理评分、W/D、BALF中的PMN值及IL-17水平均升高(P<0.05),而罗格列酮干预组肺组织炎症病理评分、W/D、BALF中的PMN值及IL-17水平在不同时间点均较LPS组降低(P<0.05)。结论罗格列酮可显著减轻LPS诱导的新生鼠肺部炎症,其机制可能与其抑制IL-17分泌相关。
引用
收藏
页码:1074 / 1080
页数:7
相关论文
共 30 条
[1]
Peripartum Antibiotics Promote Gut Dysbiosis, Loss of Immune Tolerance, and Inflammatory Bowel Disease in Genetically Prone Offspring [J].
Miyoshi, Jun ;
Bobe, Alexandria M. ;
Miyoshi, Sawako ;
Huang, Yong ;
Hubert, Nathaniel ;
Delmont, Tom O. ;
Eren, A. Murat ;
Leone, Vanessa ;
Chang, Eugene B. .
CELL REPORTS, 2017, 20 (02) :491-504
[2]
Hyaluronan ameliorates LPS-induced acute lung injury in mice via Toll-like receptor (TLR) 4-dependent signaling pathways [J].
Xu, Changqing ;
Chen, Gang ;
Yang, Weiwei ;
Xu, Yizhe ;
Xu, Yongfang ;
Huang, Xuqing ;
Liu, Jiangang ;
Feng, Yuejuan ;
Xu, Yanchun ;
Liu, Baojun .
INTERNATIONAL IMMUNOPHARMACOLOGY, 2015, 28 (02) :1050-1058
[3]
Enhanced Survival During Experimental Listeria monocytogenes Sepsis in Neonatal Mice Prophylactically Treated With Th1 and Macrophage Immunoregulatory Cytokines and Mediators [J].
Geyer, Mark B. ;
Radhakrishnan, Kavita ;
Van de Ven, Carmella ;
Suri, Mandhir S. ;
Ayello, Janet ;
Cairo, Mitchell S. .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 2014, 33 (12) :E330-E337
[4]
Glycogen synthase kinase-3β inactivation is an intracellular marker and regulator for endotoxemic neutrophilia.[J].Tsan-Tzu Yang;Chia-Ling Chen;Wei-Chieh Lin;Yee-Shin Lin;Po-Chun Tseng;Chia-Yuan Hsieh;Yu-Hong Chen;Wei-Ching Huang;Cheng-Chieh Tsai;Chi-Yun Wang;Chi-Chang Shieh;Chiou-Feng Lin.Journal of Molecular Medicine.2013, 2
[5]
Alanyl-glutamine resolves lipopolysaccharide-induced lung injury in mice by modulating the polarization of regulatory T cells and T helper 17 cells.[J].Yu-Chen Hou;Man-Hui Pai;Jun-Jen Liu;Sung-Ling Yeh.The Journal of Nutritional Biochemistry.2013,
[6]
Nasal Colonization among Premature Infants Treated with Nasal Continuous Positive Airway Pressure [J].
Aly, Hany ;
Hammad, Tarek A. ;
Ozen, Maide ;
Sandhu, Inderjeet ;
Taylor, Chita ;
Olaode, Adenike ;
Mohamed, Mohamed ;
Keiser, John .
AMERICAN JOURNAL OF PERINATOLOGY, 2011, 28 (04) :315-320
[7]
Peroxisome Proliferator-Activated Receptors as Novel Targets in Lung Disease*.[J].Maria G. Belvisi;David J. Hele.Chest.2008, 1
[8]
An overview on biological mechanisms of PPARs.[J].Bhavani Prasad Kota;Tom Hsun-Wei Huang;Basil D Roufogalis.Pharmacological Research.2004, 2
[9]
Respiratory syncytial virus infection does not increase allergen-induced type 2 cytokine production, yet increases airway hyperresponsiveness in mice [J].
Peebles, RS ;
Sheller, JR ;
Collins, RD ;
Jarzecka, AK ;
Mitchell, DB ;
Parker, RA ;
Graham, BS .
JOURNAL OF MEDICAL VIROLOGY, 2001, 63 (02) :178-188
[10]
内毒素经不同给药途径建立新生鼠急性肺损伤模型对比分析 [J].
罗艳 ;
李清香 ;
曹云涛 .
现代医药卫生, 2018, 34 (21) :3290-3294