Disruption of vascular endothelial homeostasis by tobacco smoke - impact on atherosclerosis

被引:72
作者
Bernhard, D
Pfister, G
Huck, CW
Kind, M
Salvenmoser, W
Bonn, GK
Wick, G
机构
[1] Austrian Acad Sci, Inst Biomed Aging Res, A-6020 Innsbruck, Austria
[2] Leopold Franzens Univ Innsbruck, Inst Analyt Chem & Radiochem, A-6020 Innsbruck, Austria
[3] Leopold Franzens Univ Innsbruck, Inst Zool & Limnol, A-6020 Innsbruck, Austria
关键词
smoking; cell death; statin; aging; POLYCYCLIC AROMATIC-HYDROCARBONS; CIGARETTE-SMOKING; APOPTOSIS; CELL; MECHANISMS; NICOTINE; INHIBITION; EXPRESSION; NECROSIS; DISEASE;
D O I
10.1096/fj.03-0312fje
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The World Health Organization (WHO) predicts that by 2020 tobacco will become the largest single health problem worldwide and will cause an estimated 8.4 million deaths annually (http://www5.who.int/tobacco/). Although the impact of smoking on human health is well defined from the medical point of view, surprisingly little is known about the mechanisms by which tobacco smoke mediates its disastrous effects. Here, we demonstrate that tobacco smoke dramatically changes vascular endothelial cell and tissue morphology, leading to a loss of endothelial barrier function within minutes. Long-term exposure of endothelial cells to tobacco smoke extracts induces necrosis that may trigger a pro-inflammatory status of the vessel wall. Pre-incubation of the extracts without cells for 6 h at 37degreesC led to a complete loss of activity. Further, the endothelium could be rescued by changing to fresh medium even at times when the extracts had lost their activity. Finally, we show that N-acetyl cysteine and statins inhibit the adverse tobacco smoke effects.
引用
收藏
页码:2302 / +
页数:21
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