The lectin-like oxidized low-density lipoprotein receptor-1 as therapeutic target for atherosclerosis, inflammatory conditions and longevity

被引:12
|
作者
Ulrich-Merzenich, Gudrun [1 ]
Zeitler, Heike [2 ]
机构
[1] Univ Bonn, UKB Med Clin 3, D-53127 Bonn, Germany
[2] Univ Bonn, UKB Med Clin 1, D-53127 Bonn, Germany
关键词
atherosclerosis; cardiovascular diseases; imipramine; inflammation; LOX-1; antibodies; receptor; omics; salicyclic acid; ACUTE CORONARY SYNDROME; DRUG-DELIVERY SYSTEM; C-REACTIVE PROTEIN; LOX-1; EXPRESSION; ENDOTHELIAL DYSFUNCTION; OXIDATIVE STRESS; GENE-EXPRESSION; LDL RECEPTOR; OX-LDL; ORAL BIOAVAILABILITY;
D O I
10.1517/14728222.2013.805748
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: The lectin-like oxidized LDL receptor-1 (LOX-1) is a scavenger receptor and is regarded as a central element in the initiation of endothelial dysfunction and its further progression to atherosclerosis. Increasing numbers of studies suggest that therapeutic strategies to modulate LOX-1 will have a broad spectrum of applications ranging from cardiovascular diseases to longevity. Areas covered: The dual role of LOX-1 as a culprit molecule in the process of atherosclerosis and as a danger signal in various tissues is introduced. The structure of the receptor, its ligands and its modulation by known drugs, by natural products (e. g., statins, imipramine, salicylate-based drugs, procyanidins, curcumin) and by new strategies (antisenseRNA, miRNA, pyrrole-imidazol-polyamides, LOX-1 antibodies, lipid apheresis) are described. Expert opinion: Therapeutic approaches via transcript regulation, allowing a modulation of LOX-1, may be an easier and safer strategy than a blockade of the receptor. Considering the wide distribution of LOX-1 on different tissues, research on the mechanisms of LOX-1 modulation by drugs and natural products applying "omic"-technologies will not only allow a better understanding of the role of LOX-1 in the processes of atherosclerosis, inflammation and longevity but also support the development of specific LOX-1 modulators, avoiding the initiation of molecular mechanisms which lead to adverse events.
引用
收藏
页码:905 / 919
页数:15
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