Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz

Logo MUG-Forschungsportal

Gewählte Publikation:

Kostner, GM; Krempler, F; Dieplinger, H; Zechner, R; Teubl, I; Sandhofer, F.
Altered metabolism of low density lipoprotein in humans after prolonged incubation in plasma.
Clin Sci (Lond). 1985; 68(4):411-418 Doi: 10.1042/cs0680411
Web of Science PubMed FullText FullText_MUG Google Scholar

 

Führende Autor*innen der Med Uni Graz
Kostner Gerhard
Altmetrics:

Dimensions Citations:

Plum Analytics:

Scite (citation analytics):

Abstract:
Lecithin: cholesterol acyltransferase (LCAT) in combination with exchange and transfer proteins is known to alter the composition of all plasma lipoprotein fractions. Human plasma from healthy donors was incubated for 24 h at 37 degrees C in the absence and at 4 degrees C and at 37 degrees C in the presence of the LCAT inhibitors sodium iodoacetate (5 mmol/l), and the low density lipoprotein fractions (LDL) were isolated. LDL isolated from LCAT-active plasma (LDL-a) exhibited pronounced alterations in their surface material: the relative content of phospholipids and of free cholesterol was reduced and the content of tetramethylurea-soluble apolipoproteins was increased. LDL isolated from plasma incubated at 37 degrees C with or without sodium iodoacetate showed significantly increased triglyceride concentrations. The LDL fractions from LCAT-active and LCAT-inactive (LDL-i) incubates were iodinated with 125I and 131I respectively, and their metabolic behaviour was studied in humans. LDL-a was cleared from circulation at a slower rate as compared with LDL-i (t 1/2 = 3.17 +/- 0.47 vs 2.88 +/- 0.45 days). The apparent fractional catabolic rate of LDL-a, calculated according to a two-pool model, was reduced by 22.2 +/- 3.1%. Comparing LDL-a with LDL isolated from LCAT-inactive plasma which had been incubated at 37 degrees C, the changes in the metabolic variables were less pronounced. It is concluded that physiological alterations of the chemical compositions, caused by LCAT and exchange/transfer proteins, influence the metabolism of LDL.
Find related publications in this database (using NLM MeSH Indexing)
Adult -
Apolipoproteins - blood
Cholesterol - blood
Electrophoresis, Polyacrylamide Gel - blood
Female - blood
Humans - blood
Iodoacetates - pharmacology
Iodoacetic Acid - pharmacology
Lipoproteins, LDL - blood
Lipoproteins, VLDL - blood
Male - blood
Middle Aged - blood
Phosphatidylcholine-Sterol O-Acyltransferase - antagonists and inhibitors
Temperature - antagonists and inhibitors
Time Factors - antagonists and inhibitors
Triglycerides - blood

© Med Uni Graz Impressum