Impaired high-density lipoprotein anti-oxidant capacity in human abdominal aortic aneurysm

被引:47
|
作者
Delbosc, Sandrine [1 ,2 ]
Diallo, Devy [1 ,2 ]
Dejouvencel, Tiphaine [1 ,2 ]
Lamiral, Zohra [3 ,4 ]
Louedec, Liliane [1 ,2 ]
Martin-Ventura, Jose-Luis [5 ]
Rossignol, Patrick [3 ]
Leseche, Guy [2 ,6 ]
Michel, Jean-Baptiste [1 ,2 ,7 ]
Meilhac, Olivier [1 ,2 ,8 ]
机构
[1] Hop Bichat Claude Bernard, INSERM, U698, F-75018 Paris, France
[2] Univ Paris 07, Paris, France
[3] Univ Lorraine, CHU Nancy, CIC, CIC9501,Fac Med,Inserm,U961, Vandoeuvre Les Nancy, France
[4] Hop Europeen Georges Pompidou, Serv Med Vasc & Hypertens, Paris, France
[5] Univ Autonoma Madrid, Vasc Res Lab, IIS Fdn Jimenez Diaz, Madrid, Spain
[6] Hop Xavier Bichat Claude Bernard, APHP, Serv Chirurg Thorac & Vasc, Paris, France
[7] AP HP, F-75018 Paris, France
[8] AP HP, Dept Neurol, Bichat Stroke Ctr, F-75018 Paris, France
关键词
Abdominal aortic aneurysm; Oxidative stress; Haemoglobin; High-density lipoproteins; APOLIPOPROTEIN-A-I; HUMAN ATHEROSCLEROTIC LESIONS; OXIDATIVE STRESS; CARDIOVASCULAR-DISEASE; MURAL THROMBUS; OXIDIZED LDL; HDL; ACTIVATION; APOPTOSIS; PROTEIN;
D O I
10.1093/cvr/cvt194
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Abdominal aortic aneurysm (AAA) is a particular form of atherothrombotic disease characterized by the dilation of the aortic wall and the presence of an intraluminal thrombus (ILT). The objective of the present study was to evaluate the pro-oxidant properties of the ILT and to characterize the anti-oxidant capacity of high-density lipoproteins (HDLs). Our results show that ILT, adventitia, and plasma from AAA patients contained high concentrations of lipid and protein oxidation products. Mediators produced within or released by the thrombus and the adventitia were shown to induce reactive oxygen species (ROS) production by cultured aortic smooth muscle cells (AoSMCs) and to trigger the onset of apoptosis (an increase in mitochondrial membrane potential). Iron chelation limited these effects. Both concentration and functionality of HDLs were altered in AAA patients. Plasma levels of Apo A-I were lower, and small HDL subclasses were decreased in AAA patients. Circulating HDLs in AAA patients displayed an impaired capacity to inhibit copper-induced low-density lipoprotein oxidation and AoSMC ROS production. Western blot analyses of HDLs demonstrated that myeloperoxidase is associated with HDL particles in AAA patients. ILT and adventitia are a source of pro-oxidant products, in particular haemoglobin, which may impact on the wall stability/rupture in AAA. In addition, HDLs from AAA patients exhibit an impaired anti-oxidant activity. In this context, restoring HDL functionality may represent a new therapeutic option in AAA.
引用
收藏
页码:307 / 315
页数:9
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