Monteiro-Riviere Nancy A, Inman Alfred O, Riviere Jim E
Center for Chemical Toxicology Research and Pharmacokinetics, North Carolina State University, Raleigh, NC 27606, USA.
Toxicol Appl Pharmacol. 2004 Mar 15;195(3):339-47. doi: 10.1016/j.taap.2003.07.013.
Topical exposure to jet fuel is a significant occupational hazard. Recent studies have focused on dermal absorption of fuel and its components, or alternatively, on the biochemical or immunotoxicological sequelae to exposure. Surprisingly, morphological and ultrastructural analyses have not been systematically conducted. Similarly, few studies have compared responses in skin to that of the primary target organ, the lung. The focus of the present investigation was 2-fold: first, to characterize the ultrastructural changes seen after topical exposure to moderate doses (335 or 67 microl/cm2) of jet fuels [Jet A, Jet Propellant (JP)-8, JP-8+100] for up to 4 days in pigs, and secondly, to determine if co-administration of substance P (SP) with JP-8 jet fuel in human epidermal keratinocyte cell cultures modulates toxicity as it does to pulmonary toxicity in laboratory animal studies. The primary change seen after exposure to all fuels was low-level inflammation accompanied by formation of lipid droplets in various skin layers, mitochondrial and nucleolar changes, cleft formation in the intercellular lipid lamellar bilayers, as well as disorganization in the stratum granulosum-stratum corneum interface. An increased number of Langerhans cells were also noted in jet fuel-treated skin. These changes suggest that the primary effect of jet fuel exposure is damage to the stratum corneum barrier. SP administration decreased the release of interleukin (IL)-8 normally seen in keratinocytes after JP-8 exposure, a response similar to that reported for SP's effect on JP-8 pulmonary toxicity. These studies provide a base upon which biochemical and immunological data collected in other model systems can be compared.
局部接触喷气燃料是一种重大的职业危害。最近的研究集中在燃料及其成分的皮肤吸收,或者接触后的生化或免疫毒理学后果。令人惊讶的是,尚未系统地进行形态学和超微结构分析。同样,很少有研究比较皮肤与主要靶器官肺的反应。本研究的重点有两个方面:第一,描述猪局部暴露于中等剂量(335或67微升/平方厘米)喷气燃料[喷气A、喷气推进剂(JP)-8、JP-8+100]长达4天后出现的超微结构变化;第二,确定在人表皮角质形成细胞培养物中,物质P(SP)与JP-8喷气燃料共同给药是否像在实验动物研究中对肺毒性那样调节毒性。接触所有燃料后观察到的主要变化是低水平炎症,伴有各皮肤层脂质小滴形成、线粒体和核仁变化、细胞间脂质双层中裂隙形成,以及颗粒层-角质层界面紊乱。在喷气燃料处理的皮肤中还发现朗格汉斯细胞数量增加。这些变化表明,喷气燃料暴露的主要影响是对角质层屏障的损害。给予SP可降低JP-8暴露后角质形成细胞中通常出现的白细胞介素(IL)-8释放,这一反应与报道的SP对JP-8肺毒性的作用相似。这些研究为比较其他模型系统中收集的生化和免疫学数据奠定了基础。