Net lipid transfer between lipoproteins in fish-eye disease plasma supplemented with normal high density lipoproteins
- PMID: 3600207
- DOI: 10.1007/BF02533997
Net lipid transfer between lipoproteins in fish-eye disease plasma supplemented with normal high density lipoproteins
Abstract
Native fish-eye disease plasma, which is deficient of both high density lipoproteins (HDL) and lecithin-cholesterol acyltransferase activity (alpha-LCAT), processing the free cholesterol of these lipoproteins, has been supplemented with normal isolated HDL2 or HDL3 and incubated in vitro at 37 C. After incubation for 0, 7.5 and 24 hr the very low density (VLDL) and low density (LDL) lipoproteins as well as HDL were isolated, and their contents of triglycerides, phospholipids and free, esterified and total cholesterol were quantified. The resulting net mass transfer of the different lipids revealed a functioning transfer of cholesteryl esters and all other analyzed lipids between the lipoproteins, although no de novo esterification of the HDL cholesterol by LCAT in this plasma occurred. In accordance with previous findings there was a functioning esterification process of the free cholesterol of the combined VLDL and LDL of fish-eye disease plasma. The present reports make it reasonable to conclude that the lack of HDL cholesterol esterification in this disease is not a result of a deficiency of cholesteryl ester transfer or lipid transfer activities.
Similar articles
-
Normalization of high density lipoprotein in fish eye disease plasma by purified normal human lecithin: cholesterol acyltransferase.Lipids. 1988 Mar;23(3):225-9. doi: 10.1007/BF02535462. Lipids. 1988. PMID: 3374277
-
Cholesteryl ester transfer activity in plasma of patients with familial high-density lipoprotein deficiency.Clin Chem. 1988 Sep;34(9):1812-5. Clin Chem. 1988. PMID: 3416429
-
Evidence for deficiency of high density lipoprotein lecithin: cholesterol acyltransferase activity (alpha-LCAT) in fish eye disease.Acta Med Scand. 1985;218(2):189-96. doi: 10.1111/j.0954-6820.1985.tb08846.x. Acta Med Scand. 1985. PMID: 4061122
-
Familial LCAT deficiency and fish-eye disease.J Inherit Metab Dis. 1988;11 Suppl 1:45-56. doi: 10.1007/BF01800570. J Inherit Metab Dis. 1988. PMID: 3141686 Review.
-
Body cholesterol removal: role of plasma high-density lipoproteins.Adv Lipid Res. 1980;17:1-51. Adv Lipid Res. 1980. PMID: 6992524 Review. No abstract available.
Cited by
-
Two different allelic mutations in the lecithin-cholesterol acyltransferase gene associated with the fish eye syndrome. Lecithin-cholesterol acyltransferase (Thr123----Ile) and lecithin-cholesterol acyltransferase (Thr347----Met).J Clin Invest. 1992 Feb;89(2):499-506. doi: 10.1172/JCI115612. J Clin Invest. 1992. PMID: 1737840 Free PMC article.
-
Normalization of high density lipoprotein in fish eye disease plasma by purified normal human lecithin: cholesterol acyltransferase.Lipids. 1988 Mar;23(3):225-9. doi: 10.1007/BF02535462. Lipids. 1988. PMID: 3374277
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Miscellaneous