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暴露于从建筑物分离出的短密青霉(Penicillium brevicompactum Dierckx)和产黄青霉(P. chrysogenum Thom)纯化毒素的小鼠肺部的炎症和细胞毒性反应。

Inflammatory and cytotoxic responses in mouse lungs exposed to purified toxins from building isolated Penicillium brevicompactum Dierckx and P. chrysogenum Thom.

作者信息

Rand Thomas G, Giles S, Flemming J, Miller J David, Puniani Eva

机构信息

Department of Biology, Saint Mary's University, Halifax, Nova Scotia, Canada, B3H 3C3.

出版信息

Toxicol Sci. 2005 Sep;87(1):213-22. doi: 10.1093/toxsci/kfi223. Epub 2005 Jun 15.

Abstract

In vitro and in vivo studies have shown that building-associated Penicillium spores and spore extracts can induce significant inflammatory responses in lung cells and animal models of lung disease. However, because spores and spore extracts comprise mixtures of bioactive constituents often including toxins, it is impossible to resolve which constituent mediates inflammatory responses. This study examined dose-response (0.5 nM, 2.5 nM, 5.0 nM, 12.5 nM/g body weight (BW) animal) and time-course (3, 6, 24 and 48 h post instillation (PI)) relationships associated with inflammatory and cytotoxic responses in mouse lungs intratracheally instilled with pure brevianamide A, mycophenolic acid, and roquefortine C. High doses (5.0 nM and/or 12.5 nM/g BW animal) of brevianamide A and mycophenolic acid, the dominant metabolites of P. brevicompactum, and roquefortine C, the dominant metabolite of P. chrysogenum, induced significant inflammatory responses within 6 h PI, expressed as differentially elevated macrophage, neutrophil, MIP-2, TNF, and IL-6 concentrations in the bronchioalveolar lavage fluid (BALF) of intratracheally exposed mice. Macrophage and neutrophil numbers were maximal at 24 h PI; responses of the other inflammatory markers were maximal at 6 h PI. Except for macrophage numbers in mycophenolic acid-treatment animals, cells exhibited significant dose-dependent-like responses; for the chemo-/cytokine markers, dose dependency was lacking except for MIP-2 concentration in brevianamide A-treatment animals. It was also found that brevianamide A induced cytotoxicity expressed as significantly increased LDH concentration in mouse BALF, at concentrations of 12.5 nM/g BW animal and at 6 and 24 h PI. Albumin concentrations, measured as a nonspecific marker of vascular leakage, were significantly elevated in the BALF of mice treated with 12.5 nM/g nM brevianamide A/animal from 6 to 24 h PI and in > or =5.0 nM/g mycophenolic acid-treated animals at 6 to 24 h PI. These results suggest that these three toxins from Penicillium species common on damp materials in residential housing provoke compound-specific toxic responses with different toxicokinetics. Moreover, that these toxins can stimulate significant inflammatory responses in vivo might help explain some of the indoor effects associated with Penicillium spore exposures in indoor environments.

摘要

体外和体内研究表明,与建筑物相关的青霉菌孢子和孢子提取物可在肺细胞和肺部疾病动物模型中引发显著的炎症反应。然而,由于孢子和孢子提取物包含生物活性成分的混合物,其中往往含有毒素,因此无法确定是哪种成分介导了炎症反应。本研究检测了经气管内滴注纯短密青霉胺A、霉酚酸和罗克福汀C后,小鼠肺部炎症和细胞毒性反应的剂量反应关系(0.5 nM、2.5 nM、5.0 nM、12.5 nM/克体重(BW)动物)和时间进程关系(滴注后(PI)3、6、24和48小时)。短密青霉的主要代谢产物短密青霉胺A和霉酚酸以及产黄青霉的主要代谢产物罗克福汀C的高剂量(5.0 nM和/或12.5 nM/克BW动物)在滴注后6小时内引发了显著的炎症反应,表现为气管内暴露小鼠支气管肺泡灌洗液(BALF)中巨噬细胞、中性粒细胞、MIP-2、TNF和IL-6浓度的差异升高。巨噬细胞和中性粒细胞数量在滴注后24小时达到峰值;其他炎症标志物的反应在滴注后6小时达到峰值。除霉酚酸处理动物中的巨噬细胞数量外,细胞表现出显著的剂量依赖性样反应;对于趋化因子/细胞因子标志物,除短密青霉胺A处理动物中的MIP-2浓度外,缺乏剂量依赖性。还发现,在浓度为12.5 nM/克BW动物且在滴注后6和24小时时,短密青霉胺A诱导细胞毒性,表现为小鼠BALF中LDH浓度显著增加。作为血管渗漏非特异性标志物测量的白蛋白浓度,在12.5 nM/克短密青霉胺A/动物处理的小鼠BALF中,在滴注后6至24小时显著升高,在霉酚酸处理浓度≥5.0 nM/克的动物中,在滴注后6至24小时显著升高。这些结果表明,住宅潮湿材料上常见的青霉属物种产生的这三种毒素引发了具有不同毒代动力学的化合物特异性毒性反应。此外,这些毒素可在体内刺激显著的炎症反应,这可能有助于解释室内环境中与青霉孢子暴露相关的一些室内影响。

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