Gallucci Randle M, O'Dell Sijy K, Rabe Daniel, Fechter Laurence D
Department of Pharmaceutical Sciences, College of Pharmacy, The University of Oklahoma Health Sciences Center, P.O. Box 26901, Oklahoma City, OK 73190, USA.
Int Immunopharmacol. 2004 Sep;4(9):1159-69. doi: 10.1016/j.intimp.2004.05.012.
The Department of Defense (DoD) has identified that one of the main complaints of personnel exposed to JP-8 jet fuel is irritant dermatitis. The purpose of this investigation is to describe the JP-8-induced inflammatory cytokine response in skin. JP-8 jet fuel or acetone control (300 microl) was applied to the denuded skin of rats once a day for 7 days. Skin samples from the exposed area were collected 2 and 24 h after the final exposure. Histological examination of skin biopsies showed neutrophilic inflammatory infiltrate. Reverse transcription-polymerase chain reaction (RT-PCR) was performed utilizing skin total RNA to examine the expression of various inflammatory cytokines. The CXC chemokine GROalpha was significantly upregulated at both time points, whereas GRObeta was only increased 2 h post final exposure. The CC chemokines MCP-1, Mip-1alpha, and eotaxin were induced at both time points, whereas Mip-1beta was induced only 24 h post exposure. Interleukins-1beta and -6 (IL-1beta and IL-6) mRNAs were significantly induced at both time points, while TNFalpha was not significantly different from control. Enzyme-linked immunosorbent assay (ELISA) of skin protein confirmed that MCP-1, TNFalpha, and IL-1beta were modulated as indicated by PCR analysis. However, skin IL-6 protein content was not increased 2 h post exposure, whereas it was significantly upregulated by jet fuel after 24 h. Data from the present study indicate that repeated (7 days) JP-8 exposure induces numerous proinflammatory cytokines in skin. The increased expression of these cytokines and chemokines may lead to increased inflammatory infiltrate in exposed skin, resulting in JP-8-induced irritant dermatitis.
美国国防部已确定,接触JP - 8喷气燃料的人员的主要投诉之一是刺激性皮炎。本研究的目的是描述JP - 8诱导的皮肤炎症细胞因子反应。将JP - 8喷气燃料或丙酮对照(300微升)每天一次涂抹于大鼠的裸露皮肤上,持续7天。在最后一次暴露后2小时和24小时收集暴露区域的皮肤样本。皮肤活检的组织学检查显示有嗜中性粒细胞炎性浸润。利用皮肤总RNA进行逆转录 - 聚合酶链反应(RT - PCR),以检测各种炎性细胞因子的表达。CXC趋化因子GROα在两个时间点均显著上调,而GROβ仅在最后一次暴露后2小时增加。CC趋化因子MCP - 1、Mip - 1α和嗜酸性粒细胞趋化因子在两个时间点均被诱导,而Mip - 1β仅在暴露后24小时被诱导。白细胞介素 - 1β和 - 6(IL - 1β和IL - 6)的mRNA在两个时间点均显著诱导,而TNFα与对照无显著差异。皮肤蛋白的酶联免疫吸附测定(ELISA)证实,如PCR分析所示,MCP - 1、TNFα和IL - 1β受到调节。然而,皮肤IL - 6蛋白含量在暴露后2小时并未增加,而在24小时后被喷气燃料显著上调。本研究数据表明,重复(7天)暴露于JP - 8会在皮肤中诱导多种促炎细胞因子。这些细胞因子和趋化因子表达的增加可能导致暴露皮肤中炎性浸润增加,从而导致JP - 8诱导的刺激性皮炎。