Gewählte Publikation:
Winkler, K; Nauck, M; Siekmeier, R; März, W; Wieland, H.
Determination of triglycerides in lipoproteins separated by agarose gel electrophoresis.
J Lipid Res. 1995; 36(8):1839-1847
Doi: 10.1016/S0022-2275(20)41502-0
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
Google Scholar
- Co-Autor*innen der Med Uni Graz
-
März Winfried
- Altmetrics:
- Dimensions Citations:
- Plum Analytics:
- Scite (citation analytics):
- Abstract:
- We developed a simple method for the quantitation of triglycerides in electrophoretically separated lipoproteins by specific enzymatic staining. After electrophoresis, glycerol is liberated from triglycerides by the action of cholesterol esterase. Glycerol is oxidized by a sequence of enzymatic reactions. Due to the presence of triosephosphate isomerase and glyceraldehyde-3-phosphate dehydrogenase in the reaction mixture, two moles of the precipitating dye formazane are generated per mole glycerol. The relative amounts of alpha, pre-beta, and beta lipoproteins are determined by densitometric scanning at 570 nm. Absolute triglyceride concentrations of the respective lipoprotein fractions are calculated from total triglycerides. When tested with purified very low density lipoproteins, the electrophoresis assay was linear between 0.08 and 6.5 g/l pre-beta lipoprotein triglycerides. The intra-assay and inter-assay coefficients of variation were between 5.2% and 9.8%, and between 3.2% and 12.9%, respectively. Comparison of the electrophoresis method with a combined ultracentrifugation/precipitation method in 172 sera resulted in the following correlation coefficients: alpha lipoprotein versus high density lipoprotein triglycerides, r = 0.847; pre-beta lipoprotein versus very low density lipoprotein triglycerides, r = 0.989; beta lipoprotein versus low density lipoprotein triglycerides, r = 0.815. This method is easy to perform, and is a precise and accurate technique for the determination of lipoprotein triglycerides. It is the first reliable method that allows the direct quantification of LDL triglycerides without ultracentrifugation.
- Find related publications in this database (using NLM MeSH Indexing)
-
Analysis of Variance -
-
Cholesterol - analysis
-
Electrophoresis, Agar Gel - analysis
-
Female - analysis
-
Glyceraldehyde-3-Phosphate Dehydrogenases - metabolism
-
Humans - metabolism
-
Lipoproteins - blood
-
Male - blood
-
Precipitation - blood
-
Staining and Labeling - methods
-
Triglycerides - analysis
-
Triose-Phosphate Isomerase - metabolism
-
Ultracentrifugation - metabolism
- Find related publications in this database (Keywords)
-
LIPOPROTEIN ELECTROPHORESIS
-
ENZYMATIC STAINING
-
ATHEROSCLEROSIS