Toxicity of jet fuel aliphatic and aromatic hydrocarbon mixtures on human epidermal Keratinocytes: evaluation based on in vitro cytotoxicity and interleukin-8 release

被引:0
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作者
Jen-Hung Yang
Chia-Hue Lee
Nancy A. Monteiro-Riviere
Jim E. Riviere
Chau-Loong Tsang
Chi-Chung Chou
机构
[1] Chung-Shan Medical University Hospital,Department of Dermatology
[2] National Chung-Hsing University,Veterinary Medical Teaching Hospital and Department of Veterinary Medicine, College of Veterinary Medicine
[3] North Carolina State University,Center for Chemical Toxicology Research and Pharmacokinetics (CCTRP)
[4] National Chung-Hsing University,College of Veterinary Medicine
来源
Archives of Toxicology | 2006年 / 80卷
关键词
Hydrocarbon mixtures; Jet fuels; Keratinocyte; Cytotoxicity; Interleukin-8;
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摘要
Jet fuels are complex mixtures of aliphatic (ALI) and aromatic (ARO) hydrocarbons that vary significantly in individual cytotoxicity and proinflammatory activity in human epidermal keratinocytes (HEK). In order to delineate the toxicological interactions among individual hydrocarbons in a mixture and their contributions to cutaneous toxicity, nine ALI and five ARO hydrocarbons were each divided into five (high/medium/low cytotoxic and strong/weak IL-8 induction) groups and intra/inter-mixed to assess for their mixture effects on HEK mortality and IL-8 release. Addition of single hydrocarbon to JP-8 fuel was also evaluated for their changes in fuel dermatotoxicity. The results indicated that when hydrocarbons were mixed, HEK mortality and IL-8 release were not all predictable by their individual ability affecting these two parameters. The lowest HEK mortality (7%) and the highest IL-8 production were induced with mixtures including high cytotoxic and weak IL-8 inductive ARO hydrocarbons. Antagonistic reactions not consistently correlated with ALI carbon chain length and ARO structure were evident and carried different weight in the overall mixture toxicities. Single addition of benzene, toluene, xylene or ethylbenzene for up to tenfold in JP-8 did not increase HEK mortality while single addition of ALI hydrocarbons exhibited dose-related differential response in IL-8. In an all ALI environment, no single hydrocarbon is the dominating factor in the determination of HEK cytotoxicity while deletion of hexadecane resulted in a 2.5-fold increase in IL-8 production. Overall, decane, undecane and dodecane were the major hydrocarbons associated with high cytotoxicity while tetradecane, pentadecane and hexadecane were those which had the greatest buffering effect attenuating dermatotoxicity. The mixture effects must be considered when evaluating jet fuel toxicity to HEK.
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页码:508 / 523
页数:15
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