Systemic molecular and cellular changes induced in rats upon inhalation of JP-8 petroleum fuel vapor

被引:6
|
作者
Hanas, Jay S. [1 ,2 ,3 ]
Briggs, G. Bruce [4 ]
Lerner, Megan R. [2 ,3 ]
Lightfoot, Stan A. [2 ,3 ]
Larabee, Jason L. [1 ]
Karsies, Todd J. [1 ]
Epstein, Robert B. [5 ]
Hanas, Rushie J. [1 ]
Brackett, Daniel J. [2 ,3 ]
Hocker, James R. [1 ]
机构
[1] Univ Oklahoma, Hlth Sci Ctr, Dept Biochem & Mol Biol, Oklahoma City, OK 73104 USA
[2] Univ Oklahoma, Hlth Sci Ctr, Dept Surg, Oklahoma City, OK 73104 USA
[3] Vet Affairs Med Ctr, Oklahoma City, OK 73104 USA
[4] USN, Med Res Inst Toxicol Detachment, Wright Patterson AFB, OH 45433 USA
[5] Univ Oklahoma, Hlth Sci Ctr, Dept Med, Oklahoma City, OK 73104 USA
关键词
JP-8 inhalation rat model; petroleum/hydrocarbon-induced heart damage; toxicity biomarkers; mass spectrometry; cDNA arrays; JET FUEL; DERMAL EXPOSURE; EXPRESSION; APOPTOSIS; TOXICITY; STRESS; HEART; RISK;
D O I
10.3109/15376511003681009
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Limited information is available regarding systemic changes in mammals associated with exposures to petroleum/hydrocarbon fuels. In this study, systemic toxicity of JP-8 jet fuel was observed in a rat inhalation model at different JP-8 fuel vapor concentrations (250, 500, or 1000 mg/m(3), for 91 days). Gel electrophoresis and mass spectrometry sequencing identified the alpha-2 microglobulin protein to be elevated in rat kidney in a JP-8 dose-dependent manner. Western blot analysis of kidney and lung tissue extracts revealed JP-8 dependent elevation of inducible heat shock protein 70 (HSP70). Tissue changes were observed histologically (hematoxylin and eosin staining) in liver, kidney, lung, bone marrow, and heart, and more prevalently at medium or high JP-8 vapor phase exposures (500-1000 mg/m(3)) than at low vapor phase exposure (250 mg/m(3)) or non-JP-8 controls. JP-8 fuel-induced liver alterations included dilated sinusoids, cytoplasmic clumping, and fat cell deposition. Changes to the kidneys included reduced numbers of nuclei, and cytoplasmic dumping in the lumen of proximal convoluted tubules. JP-8 dependent lung alterations were edema and dilated alveolar capillaries, which allowed clumping of red blood cells (RBCs). Changes in the bone marrow in response to JP-8 included reduction of fat cells and fat globules, and cellular proliferation (RBCs, white blood cells-WBCs, and megakaryocytes). Heart tissue from JP-8 exposed animals contained increased numbers of inflammatory and fibroblast cells, as well as myofibril scarring. cDNA array analysis of heart tissue revealed a JP-8 dependent increase in atrial natriuretic peptide precursor mRNA and a decrease in voltage-gated potassium (K+) ion channel mRNA.
引用
收藏
页码:204 / 212
页数:9
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