Antiatherogenic functionality of high density lipoprotein: how much versus how good
- PMID: 18385533
- DOI: 10.5551/jat.e571
Antiatherogenic functionality of high density lipoprotein: how much versus how good
Abstract
Plasma concentration of high density lipoprotein (HDL) is one of the most reliable negative risk factors for CVD. There is however convincing experimental and clinical evidence that plasma concentration of HDL does not convey the full picture of atheroprotective properties of HDL. HDL functionality, i.e. the ability of HDL to perform its many atheroprotective functions, is partly independent of HDL concentration and may be as important, if not more important, in determining the atheroprotective capacity of HDL. The capacity of HDL to support cholesterol efflux, its anti-inflammatory, anti-oxidant, anti-thrombotic and other atheroprotective functions are affected dramatically in conditions like coronary artery disease, chronic and acute inflammation, diabetes as well as through various interventions. The mechanisms connecting changes in HDL functionality to HDL structure are only beginning to emerge. Modifications of HDL proteins and lipids, such as advanced glycation and oxidation, changes in HDL composition and size of HDL particles, changes in abundance of various proteins and lipids carried by HDL are among factors affecting HDL functionality. A single common denominator reflecting the multiple HDL functions is yet to be found and may not exist leaving direct measurements of each HDL function as the way to assess atheroprotective capacity of HDL.
Similar articles
-
Small, dense high-density lipoprotein-3 particles are enriched in negatively charged phospholipids: relevance to cellular cholesterol efflux, antioxidative, antithrombotic, anti-inflammatory, and antiapoptotic functionalities.Arterioscler Thromb Vasc Biol. 2013 Dec;33(12):2715-23. doi: 10.1161/ATVBAHA.113.301468. Epub 2013 Oct 3. Arterioscler Thromb Vasc Biol. 2013. PMID: 24092747
-
Dysfunctional HDL as a Therapeutic Target for Atherosclerosis Prevention.Curr Med Chem. 2019;26(9):1610-1630. doi: 10.2174/0929867325666180316115726. Curr Med Chem. 2019. PMID: 29546829 Review.
-
Dual effect of hypochlorite in the modification of high density lipoproteins.Biochem Biophys Res Commun. 2010 Dec 17;403(3-4):447-51. doi: 10.1016/j.bbrc.2010.11.053. Epub 2010 Nov 19. Biochem Biophys Res Commun. 2010. PMID: 21094143
-
[Molecular Mechanism and Evaluation Method for Anti-Inflammatory HDL].Rinsho Byori. 2016 Jan;64(1):49-56. Rinsho Byori. 2016. PMID: 27192797 Review. Japanese.
-
Current Therapies Focused on High-Density Lipoproteins Associated with Cardiovascular Disease.Molecules. 2018 Oct 23;23(11):2730. doi: 10.3390/molecules23112730. Molecules. 2018. PMID: 30360466 Free PMC article. Review.
Cited by
-
High-density lipoproteins attenuate high glucose-impaired endothelial cell signaling and functions: potential implications for improved vascular repair in diabetes.Cardiovasc Diabetol. 2017 Sep 29;16(1):121. doi: 10.1186/s12933-017-0605-8. Cardiovasc Diabetol. 2017. PMID: 28962618 Free PMC article.
-
Associations Between High Levels of High-Density Lipoprotein Cholesterol and the Presence and Severity of Coronary Artery Disease in Patients Who Have Undergone Coronary Computed Tomography Angiography.J Clin Med Res. 2020 Nov;12(11):734-739. doi: 10.14740/jocmr4367. Epub 2020 Nov 3. J Clin Med Res. 2020. PMID: 33224375 Free PMC article.
-
Anti-oxidant properties of high-density lipoprotein and atherosclerosis.Clin Exp Pharmacol Physiol. 2010 Jul;37(7):719-25. doi: 10.1111/j.1440-1681.2010.05380.x. Epub 2010 Mar 30. Clin Exp Pharmacol Physiol. 2010. PMID: 20374263 Free PMC article. Review.
-
Effect of foreign surface pacification with albumin, aprotinin, propofol, and high-density lipoprotein.J Extra Corpor Technol. 2009 Mar;41(1):3-9. J Extra Corpor Technol. 2009. PMID: 19361025 Free PMC article.
-
Structure of apolipoprotein A-I N terminus on nascent high density lipoproteins.J Biol Chem. 2011 Jan 28;286(4):2966-75. doi: 10.1074/jbc.M110.163097. Epub 2010 Nov 3. J Biol Chem. 2011. PMID: 21047795 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical