Short-term exposure to particulate matter induces arterial but not venous thrombosis in healthy mice

被引:36
|
作者
Emmerechts, J. [1 ]
Alfaro-Moreno, E. [2 ,3 ]
Vanaudenaerde, B. M. [4 ,5 ]
Nemery, B. [2 ]
Hoylaerts, M. F. [1 ]
机构
[1] Katholieke Univ Leuven, Ctr Mol & Vasc Biol, B-3000 Louvain, Belgium
[2] Katholieke Univ Leuven, Unit Lung Toxicol, B-3000 Louvain, Belgium
[3] Inst Nacl Cancerol, Subdirecc Invest Basica, Mexico City, DF, Mexico
[4] Katholieke Univ Leuven, Lung Transplantat Unit, B-3000 Louvain, Belgium
[5] Univ Hosp Gasthuisberg, B-3000 Louvain, Belgium
关键词
air pollution; coagulation; inflammation; particulate matter; DIESEL EXHAUST INHALATION; AIR-POLLUTION; INFLAMMATORY RESPONSES; PULMONARY INFLAMMATION; LUNG INFLAMMATION; BLOOD-COAGULATION; OXIDATIVE STRESS; HUMAN VOLUNTEERS; HEART-DISEASE; MOUSE LUNG;
D O I
10.1111/j.1538-7836.2010.04081.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Epidemiological findings suggest an association between exposure to particulate matter (PM) and venous thrombo-embolism. Objectives: To investigate arterial vs. venous thrombosis, inflammation and coagulation in mice, (sub) acutely exposed to two types of PM. Methods: Various doses (25, 100 and 200 mu g per animal) of urban particulate matter (UPM) or diesel exhaust particles (DEP) were intratracheally (i.t.) instilled in C57B16/n mice and several endpoints measured at 4, 10 and 24 h. Mice were also repeatedly exposed to 100 mu g per animal on three consecutive days with endpoints measured 24 h after the last instillation. Results: Exposure to 200 mu g per mouse UPM enhanced arterial thrombosis, but neither UPM nor DEP significantly enhanced venous thrombosis. Both types of PM induced dose-dependent increases in broncho-alveolar lavage fluid (BALF) total cell numbers (mainly neutrophils) and cytokines (IL-6, KC, MCP-1, RANTES, MIP-1 alpha), with peaks at 4 h and overall higher values for UPM than for DEP. Systemic inflammation was limited to increased serum IL-6 levels, 4 h after UPM. Both types of PM induced similar and dose-dependent but modest increases in factor (F) VII, FVIII and fibrinogen. Three repeated instillations did not or only modestly enhance the proinflammatory and procoagulant status. Conclusions: Compared with DEP, UPM induced more pronounced pulmonary inflammation, but both particle types triggered similar and mild short-term systemic effects. Hence, acute exposure to PM triggers activation of primary hemostasis in the mouse, but no substantial secondary hemostasis activation, resulting in arterial but not venous thrombogenicity.
引用
收藏
页码:2651 / 2661
页数:11
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