Suppr超能文献

吡非尼酮在博来霉素诱导的仓鼠肺部炎症模型中的抗炎作用。

Anti-inflammatory effect of pirfenidone in the bleomycin-hamster model of lung inflammation.

作者信息

Iyer S N, Hyde D M, Giri S N

机构信息

Department of Molecular Biosciences, School of Veterinary Medicine, University of California, Davis, USA.

出版信息

Inflammation. 2000 Oct;24(5):477-91. doi: 10.1023/a:1007068313370.

Abstract

We have previously reported the antifibrotic effects of pirfenidone (PD) in the bleomycin (BL)-hamster model of lung fibrosis. Since the development of fibrosis is generally preceded by acute lung inflammation, the present study was conducted to find out if dietary intake of PD (0.5%) has any effects on BL-induced lung inflammation. In this regard, we evaluated the effects of PD on BL-induced increased pulmonary vascular permeability, increased influx of inflammatory cells and increased levels of TGF-beta in the bronchoalveolar lavage fluid (BALF). Hamsters were intratracheally (IT) instilled with saline (SA) or BL (5.5 units/kg/5 ml). The animals were fed the control diet (CD) or the same diet containing 0.5% PD 2 days prior to IT instillation and throughout the study. The bronchoalveolar lavage was carried out at different times after IT instillation. Lavage fluid was used for total and differential cell counts and BALF-supernatant for measurement of total protein and TGF-beta. IT instillation of BL caused significant increases in total cells, neutrophils, macrophages and lymphocytes and in the levels of total protein and TGF-beta in BALF from hamsters in the BL + CD groups as compared to the corresponding SA + CD control groups. In contrast, treatment with pirfenidone in general, suppressed the BL-induced increases in the levels of proteins and TGF-beta and in the influx of neutrophils, macrophages and lymphocytes in BALF at the early time points in BL + PD groups. Based on the data reported in this study, we conclude that the anti-inflammatory effects of pirfenidone as evident by suppressions of BL-induced increased pulmonary vascular permeability and increased influx of inflammatory cells in the lung contribute additionally to its inherent anti-fibrotic effect.

摘要

我们之前报道了吡非尼酮(PD)在博来霉素(BL)诱导的仓鼠肺纤维化模型中的抗纤维化作用。由于纤维化的发展通常先于急性肺部炎症,因此进行本研究以探究饮食摄入PD(0.5%)是否对BL诱导的肺部炎症有任何影响。在这方面,我们评估了PD对BL诱导的肺血管通透性增加、炎症细胞流入增加以及支气管肺泡灌洗液(BALF)中转化生长因子-β水平升高的影响。仓鼠经气管内(IT)注入生理盐水(SA)或BL(5.5单位/千克/5毫升)。在IT注入前2天及整个研究过程中,给动物喂食对照饮食(CD)或含0.5% PD的相同饮食。在IT注入后的不同时间进行支气管肺泡灌洗。灌洗液用于进行总细胞和分类细胞计数,BALF上清液用于测量总蛋白和转化生长因子-β。与相应的SA + CD对照组相比,BL + CD组仓鼠经IT注入BL后,BALF中的总细胞、中性粒细胞、巨噬细胞和淋巴细胞以及总蛋白和转化生长因子-β水平显著增加。相比之下,在BL + PD组的早期时间点,一般用吡非尼酮治疗可抑制BL诱导的BALF中蛋白和转化生长因子-β水平升高以及中性粒细胞、巨噬细胞和淋巴细胞的流入。基于本研究报告的数据,我们得出结论,吡非尼酮的抗炎作用表现为抑制BL诱导的肺血管通透性增加和肺部炎症细胞流入增加,这进一步增强了其固有的抗纤维化作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验