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Organic chemicals in diesel exhaust particles enhance picryl chloride-induced atopic dermatitis in NC/Nga mice

机译:柴油机排气颗粒中的有机化学物质可增强NC / Nga小鼠氯化苦味酚诱导的特应性皮炎

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Background: Diesel exhaust particles (DEP) have been reported to worsen allergic airway inflammation in mice. Recently, the organic chemical components of DEP (DEP-OC) were found to be important contributors to the aggravation of allergic airway inflammation in mice. The purpose of this study was to examine the effects of DEP-OC on atopic dermatitis (AD)-like skin lesions induced by picryl chloride (PiCl) in NC/Nga mice. Methods: DEP were extracted with benzene/ethanol, and the soluble organic fraction formed the DEP-OC. NC/Nga male mice received simultaneous application of DEP-OC and/or PiCl on their ears once a week for 9 or 3 weeks. We evaluated skin lesions by noting scaling, eruption, excoriation, erosion, hemorrhage, pathologic changes, production of cytokines, and IgE level in the serum. Results: PiCl application alone produced progressively severe AD-like skin lesions. The application of PiCl plus DEP-OC resulted in a marked worsening of skin lesions in the early stages of AD. Moreover, mast cell counts significantly increased in the subcutaneous tissue. Administration of PiCl combined with DEP-OC resulted in a greater increase in the local expression of interleukin-4, keratinocyte chemoattractant, and neutrophils in subcutaneous tissue compared with PiCl treatment alone. In contrast, the combination treatment produced lower levels of IFN-γ compared with PiCl treatment alone. Conclusions: DEP-OC application to the skin aggravated PiCl-induced AD. This aggravation may be due to activation of the Th2-associated immune responses by the organic chemicals in DEP.
机译:背景:据报道,柴油机排气颗粒(DEP)可加重小鼠的过敏性气道炎症。最近,发现DEP的有机化学成分(DEP-OC)是加重小鼠过敏性气道炎症的重要因素。这项研究的目的是检查DEP-OC对NC / Nga小鼠中的氯化苦(PiCl)诱导的特应性皮炎(AD)样皮肤损伤的作用。方法:用苯/乙醇萃取DEP,可溶性有机部分形成DEP-OC。 NC / Nga雄性小鼠每周一次在耳朵上同时接受DEP-OC和/或PiCl,持续9或3周。我们通过注意结垢,喷发,脱落,糜烂,出血,病理变化,细胞因子的产生和血清中的IgE水平来评估皮肤损伤。结果:单独使用PiCl会产生逐渐严重的AD样皮肤损伤。 PiCl加DEP-OC的使用导致AD早期皮肤病变的明显恶化。此外,皮下组织中肥大细胞计数显着增加。与单独的PiCl处理相比,PiCl与DEP-OC的联合给药可导致皮下组织中白介素4,角质形成细胞趋化因子和嗜中性粒细胞的局部表达增加。相反,与单独的PiCl处理相比,联合处理产生较低水平的IFN-γ。结论:DEP-OC在皮肤上的应用加重了PiCl诱导的AD。这种恶化可能是由于DEP中有机化学物质激活了Th2相关的免疫反应。

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