Oxidized Low Density Lipoproteins-Do We Know Enough About Them?

被引:23
作者
Jiang, Xueting [1 ]
Yang, Zhaohui [1 ]
Chandrakala, Aluganti Narasimhulu [1 ]
Pressley, Dawn [1 ]
Parthasarathy, Sampath [1 ]
机构
[1] Ohio State Univ, Div Cardiac Surg, Med Ctr, Columbus, OH 43210 USA
关键词
Atherosclerosis; Lipid peroxidation; Scavenger receptors; Aldehydes; Lipid peroxides; Antioxidants; ENHANCED MACROPHAGE DEGRADATION; HUMAN ATHEROSCLEROTIC LESIONS; HUMAN ENDOTHELIAL-CELLS; ACETYL-LDL RECEPTOR; LIPID-PEROXIDATION; OXIDATIVE MODIFICATION; DEFICIENT MICE; BINDING-SITE; IN-VIVO; MYELOPEROXIDASE;
D O I
10.1007/s10557-011-6326-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Since the discovery of oxidized low density lipoprotein (Ox-LDL), over 5,000 articles have appeared on the topic with over 400 articles appearing every year during the past decade. LDL contains esterified polyunsaturated fatty acid containing lipids, such as, phosphatidylcholine (PtdCho) and cholesterol esters (CE). Peroxidation of polyunsaturated fatty acid (PUFA) containing lipids has been known for a long time. Numerous studies have documented that peroxidized lipids as well as products derived from their decomposition, particularly aldehydes, have deleterious biological properties. This concept has been exemplified in the study of atherosclerosis. A plethora of in vitro and animal studies, as well as human epidemiological and correlatory studies, have supported the notion that oxidative processes and the formation of Ox-LDL might contribute to atherosclerosis. Yet the negative outcomes of human clinical trials with alpha-tocopherol and other antioxidants have convinced even staunch supporters of the hypothesis to take a step backwards and reconsider reasons of their failure and suggest alternative approaches. Ox-LDL is a complex mixture of numerous chemical entities, many of them are yet uncharacterized. Why and how it is formed or its nature in vivo is poorly understood. It is recognized by numerous cell surface receptors, which are ubiquitously expressed in many different cell types. These receptors might perform a variety of functions. In addition, components of Ox-LDL might also have favorable effects that are difficult to dissociate from its pathological effects. In this review, the nature of Ox-LDL and potential problems in inhibiting its formation are discussed.
引用
收藏
页码:367 / 377
页数:11
相关论文
共 83 条
  • [41] LYNCH SM, 1993, J LIPID RES, V34, P1745
  • [42] Marinari Umberto Maria, 2003, Molecular Aspects of Medicine, V24, P205, DOI 10.1016/S0098-2997(03)00015-3
  • [43] Expression of human myeloperoxidase by macrophages promotes atherosclerosis in mice
    McMillen, TS
    Heinecke, JW
    LeBoeuf, RC
    [J]. CIRCULATION, 2005, 111 (21) : 2798 - 2804
  • [44] Serum Myeloperoxidase levels are associated with the future risk of coronary artery disease in apparently healthy individuals - The EPIC-Norfolk prospective population study
    Meuwese, Marijn C.
    Stroes, Erik S. G.
    Hazen, Stanley L.
    van Miert, Joram N.
    Kuivenhoven, Jan Albert
    Schaub, Robert G.
    Wareham, Nicholas J.
    Luben, Robert
    Kastelein, John J. P.
    Khaw, Kay-Tee
    Boekholdt, S. Matthijs
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2007, 50 (02) : 159 - 165
  • [45] Measurement of lipid peroxidation
    Moore, K
    Roberts, LJ
    [J]. FREE RADICAL RESEARCH, 1998, 28 (06) : 659 - 671
  • [46] FORMATION OF F-2-ISOPROSTANES DURING OXIDATION OF HUMAN LOW-DENSITY-LIPOPROTEIN AND PLASMA BY PEROXYNITRITE
    MOORE, KP
    DARLEYUSMAR, V
    MORROW, J
    ROBERTS, LJ
    [J]. CIRCULATION RESEARCH, 1995, 77 (02) : 335 - 341
  • [47] The degree of unsaturation of dietary fatty acids and the development of atherosclerosis (Review)
    Moreno, JJ
    Mitjavila, MT
    [J]. JOURNAL OF NUTRITIONAL BIOCHEMISTRY, 2003, 14 (04) : 182 - 195
  • [48] STRUCTURAL DEFINITION OF EARLY LYSINE AND HISTIDINE ADDUCTION CHEMISTRY OF 4-HYDROXYNONENAL
    NADKARNI, DV
    SAYRE, LM
    [J]. CHEMICAL RESEARCH IN TOXICOLOGY, 1995, 8 (02) : 284 - 291
  • [49] LOW-DENSITY LIPOPROTEIN UNDERGOES OXIDATIVE MODIFICATION INVIVO
    PALINSKI, W
    ROSENFELD, ME
    YLAHERTTUALA, S
    GURTNER, GC
    SOCHER, SS
    BUTLER, SW
    PARTHASARATHY, S
    CAREW, TE
    STEINBERG, D
    WITZTUM, JL
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (04) : 1372 - 1376
  • [50] Increased protein nitration burden in the atherosclerotic lesions and plasma of apolipoprotein A-I-deficient mice
    Parastatidis, Ioannis
    Thomson, Leonor
    Fries, Diana M.
    Moore, Ryan E.
    Tohyama, Junichiro
    Fu, Xiaoming
    Hazen, Stanley L.
    Heijnen, Harry F. G.
    Dennehy, Michelle K.
    Liebler, Daniel C.
    Rader, Daniel J.
    Ischiropoulos, Harry
    [J]. CIRCULATION RESEARCH, 2007, 101 (04) : 368 - 376