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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.
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页码:2651 / 2661
页数:11
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