支气管肺泡灌洗
脂多糖
肺
免疫印迹
H&E染色
医学
分子生物学
化学
病理
男科
免疫学
染色
内科学
生物
生物化学
基因
作者
Shanshan Zhu,Hao Jiao,Guang Feng,Gongjian Liu
出处
期刊:International Journal of Anesthesiology and Resuscitation
[Chinese Medical Association]
日期:2012-08-15
卷期号:33 (08): 533-537
标识
DOI:10.3760/cma.j.issn.1673-4378.2012.08.008
摘要
Objective To investigate the role of Src/STAT signal pathway in LPS-induced ALI. Methods Sixty male SD rats were divided into four groups using a random number table:blank (NS) group,lipopolysaccharide (LPS) group,LPS+SU6656 (LPS+SU) group and NS+SU6656 (NS+SU) group.The concentrations of macrophage inflammatory protein 2(MIP-2) and interleukin (IL)-6 in bronchoalveolar lavage fluids (BALF) were detected by ELISA and the histopathologic changes of lung tissues were observed by hematoxylin-eosin (H-E) staining.The expression of nuclear factor kappa B(NF-κB) in nuclear extracts,phosphor-STAT and IκBα in cytoplasmic extracts were analyzed by Western blot.In addition,survival rate with the other 10 rates each group was investigated. Results The serious pulmonary inflammation and conspicuous lung damage were observed in LPS group.AS compared with LPS group,the MIP-2 and IL-6 in BALF were significantly decreased [MIP-2 reached a peak at 6 h,(1 135±209) vs (875±112),P<0.05.IL-6 reached a peak at 3 h,(2 235±267) vs(5 125±658 ),P<0.05].The histopathologic changes of lung tissues were relieved obviously.Wet / dry weight ratio of the lung was decreased.LPS+SU6656 group had a higher survival rate (37.6% vs 10.5%,P<0.05) and the NF-κB activation and the degradation of IκBα in cytoplasma were inhibited. Conclusions These data suggested that Src/STAT signal pathway plays an essential role in LPS -induced acute lung injury.SU6656,Src kinase specific inhibitor,attenuates LPS-induced lung injury via inhibiting the NF-κB activation and IκBoα degradation,indicating that the Src/STAT signal pathway may be involved in the activation of NF-κB.
Key words:
Src kinase/signal transducer and activator of transcription signal pathway; Lipopolysaccharide; Acute lung injury; Nuclear factor kappa B; SU6656; Macrophage inflammatory protein 2; Interleukin-6
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