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镉暴露大鼠的气道炎症与肺部氧化应激和肺气肿有关。

Airway inflammation in cadmium-exposed rats is associated with pulmonary oxidative stress and emphysema.

作者信息

Kirschvink Nathalie, Martin Nathalie, Fievez Laurence, Smith Nicola, Marlin David, Gustin Pascal

机构信息

Department for Functional Sciences, B41, Faculty of Veterinary Medicine, University of Liège, Liège, Belgium.

出版信息

Free Radic Res. 2006 Mar;40(3):241-50. doi: 10.1080/10715760500494657.

Abstract

The aim of this study was to test the hypothesis that pulmonary inflammation and emphysema induced by cadmium (Cd) inhalation are associated with pulmonary oxidative stress. Two groups of Sprague Dawley rats were used: one vehicle-exposed group undergoing inhalation of NaCl (0.9%, n = 24) and one Cd-exposed group undergoing inhalation of CdCl(2) (0.1%, n = 24). The animals in the vehicle-and Cd-exposed groups were divided into 4 subgroups (n = 6 per group), which underwent either a single exposure (D2) of 1H or repeated exposures 3 times/week for 1H for a period of 3 weeks (3W), 5 weeks (5W) or 5 weeks followed by 2 weeks without exposure (5W + 2). At sacrifice, the left lung was fixed for histomorphometric analysis (median inter-wall distance, MIWD), whilst bronchoalveolar lavage fluid (BALF) was collected from the right lung. Cytological analysis of BALF was performed and BALF was analysed for oxidant markers 8-iso-PGF(2a), uric acid (UA), reduced (AA) and oxidised ascorbic acid (DHA) and reduced (GSH) and oxidised glutathione (GSSG). Cd-exposure induced a significant increase of BALF macrophages and neutrophils. 8-iso-PGF(2a), UA, GSH and GSSG were significantly increased at D2. At 5W and 5W + 2, AA and GSH were significantly lower in Cd-exposed rats, indicating antioxidant depletion. MIWD significantly increased in all repeatedly Cd-exposed groups, suggesting development of pulmonary emphysema. 8-iso-PGF(2a) and UA were positively correlated with macrophage and neutrophil counts. GSH, GSSG and 8-iso-PGF(2a) were negatively correlated with MIWD, indicating that Cd-induced emphysema could be associated with pulmonary oxidative stress.

摘要

本研究的目的是检验以下假设

吸入镉(Cd)所致的肺部炎症和肺气肿与肺部氧化应激有关。使用了两组斯普拉格-道利大鼠:一组为吸入氯化钠(0.9%,n = 24)的溶剂暴露组,另一组为吸入氯化镉(0.1%,n = 24)的镉暴露组。溶剂暴露组和镉暴露组的动物被分为4个亚组(每组n = 6),分别接受单次1小时暴露(D2)或每周3次、每次1小时、持续3周(3W)、5周(5W)或5周后再停止暴露2周(5W + 2)的重复暴露。处死时,取左肺进行组织形态计量分析(壁间中值距离,MIWD),同时从右肺收集支气管肺泡灌洗液(BALF)。对BALF进行细胞学分析,并分析其氧化标志物8-异前列腺素F2α(8-iso-PGF2α)、尿酸(UA)、还原型(AA)和氧化型抗坏血酸(DHA)以及还原型(GSH)和氧化型谷胱甘肽(GSSG)。镉暴露导致BALF中巨噬细胞和中性粒细胞显著增加。在D2时,8-iso-PGF2α、UA、GSH和GSSG显著升高。在5W和5W + 2时,镉暴露大鼠的AA和GSH显著降低,表明抗氧化剂耗竭。所有重复镉暴露组的MIWD均显著增加,提示肺气肿形成。8-iso-PGF2α和UA与巨噬细胞及中性粒细胞计数呈正相关。GSH、GSSG和8-iso-PGF2α与MIWD呈负相关,表明镉诱导的肺气肿可能与肺部氧化应激有关。

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