The protein moiety of Lp[a] is widely believed to consist of one molecule of apo B-100 and one molecule of apo[a] per particle, linked by at least one disulfide bond. In this study we have re-examined the composition of Lp[a] to determine if other less abundant apolipoproteins might be present. Anal
Abnormalities in apo B-containing lipoproteins in diabetes and atherosclerosis
โ Scribed by Gerald H. Tomkin; Daphne Owens
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 176 KB
- Volume
- 17
- Category
- Article
- ISSN
- 1520-7552
- DOI
- 10.1002/dmrr.179
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โฆ Synopsis
Atherosclerosis is the major cause of death in patients with diabetes. Lowdensity lipoprotein (LDL) being the most important cholesterol-carrying lipoprotein has been studied extensively in both diabetes and non-diabetes. This paper reviews the literature but also focuses on the precursors of LDL and in particular the postprandial apo B-containing lipoproteins. Abnormalities in the postprandial lipoproteins and alteration in chylomicron assembly and clearance are discussed and the evidence presented suggesting the importance of dysregulation of these lipoproteins in atherosclerotic progression. The relationship between chylomicron production in the intestine and hepatic release of very low-density lipoproteins (VLDL) is explored, as is the interrelationship between clearance rates of these lipoproteins. The size of LDL inยฏuences its atherogenicity. VLDL composition and size in relation to its inยฏuence on LDL is discussed. The effect of diet on the composition of lipoproteins and the relationship between fatty acid composition and clearance is reviewed. Evidence that diabetic control beneยฎcially alters lipoprotein composition is presented suggesting how improved diabetic control may reduce atherosclerosis. The review concludes with a discussion on the effect of the apo B-containing lipoproteins and their modiยฎcation through glycation and oxidation on macrophage and endothelial function.
๐ SIMILAR VOLUMES
In this study, plasma HDL fractions were separated by ultracentrifugation and apo A-I containing lipoproteins (A-I Lp) were then isolated using anti-apo A-I immunoaffinity chromatography. The A-I Lp were further separated into two fractions with the use of anti-apo A-II immunoaffinity chromatography