| Literature DB >> 33260304 |
Liang-Yin Ke1,2,3, Shi Hui Law1, Vineet Kumar Mishra1, Farzana Parveen1, Hua-Chen Chan3, Ye-Hsu Lu3,4, Chih-Sheng Chu3,4,5.
Abstract
Dysregulation of glucose and lipid metabolism increases plasma levels of lipoproteins and triglycerides, resulting in vascular endothelial damage. Remarkably, the oxidation of lipid and lipoprotein particles generates electronegative lipoproteins that mediate cellular deterioration of atherosclerosis. In this review, we examined the core of atherosclerotic plaque, which is enriched by byproducts of lipid metabolism and lipoproteins, such as oxidized low-density lipoproteins (oxLDL) and electronegative subfraction of LDL (LDL(-)). We also summarized the chemical properties, receptors, and molecular mechanisms of LDL(-). In combination with other well-known markers of inflammation, namely metabolic diseases, we concluded that LDL(-) can be used as a novel prognostic tool for these lipid disorders. In addition, through understanding the underlying pathophysiological molecular routes for endothelial dysfunction and inflammation, we may reassess current therapeutics and might gain a new direction to treat atherosclerotic cardiovascular diseases, mainly targeting LDL(-) clearance.Entities:
Keywords: L5 LDL; LDL(−); LOX-1; atherosclerosis; cardiovascular disease; dyslipidemia; electronegative LDL; endothelial dysfunction; lectin-like oxLDL receptor-1; oxLDL; oxidized LDL
Year: 2020 PMID: 33260304 DOI: 10.3390/biomedicines8120550
Source DB: PubMed Journal: Biomedicines ISSN: 2227-9059