Analytical capillary isotachophoresis of total plasma lipoproteins: a new tool to identify atherogenic low density lipoproteins

Plasma low density lipoproteins from 20 patients were separated by capillary isotachophoresis (ITP). In each patient the apparent diameter of the predominant LDL peak on whole plasma was also determined by nondenaturing gradient gel electrophoresis. Furthermore the concentration of the more electron...

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Main Authors: Gabriele Bittolo-Bon, Giuseppe Cazzolato
Format: Article
Language:English
Published: Elsevier 1999-01-01
Series:Journal of Lipid Research
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S0022227520333538
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author Gabriele Bittolo-Bon
Giuseppe Cazzolato
author_facet Gabriele Bittolo-Bon
Giuseppe Cazzolato
author_sort Gabriele Bittolo-Bon
collection DOAJ
description Plasma low density lipoproteins from 20 patients were separated by capillary isotachophoresis (ITP). In each patient the apparent diameter of the predominant LDL peak on whole plasma was also determined by nondenaturing gradient gel electrophoresis. Furthermore the concentration of the more electronegatively charged in vivo oxidized LDL− was accomplished using anion exchange high pressure liquid chromatography. By analytical capillary ITP of whole plasma lipoproteins, prestained with a lipophilic dye, LDL were separated into four subfractions. Usually, the predominant subfraction was the slow migrating LDL4, followed by LDL3, and then by the faster LDL2 and LDL1. Slow migrating LDL4 correlated negatively with plasma triglycerides and LDL− and positively with plasma high density lipoprotein (HDL) cholesterol and with the LDL diameter, while the faster LDL1 showed an inverse behavior. The LDL1 + LDL2 to LDL3 + LDL4 ratio showed a strong positive correlation with LDL− concentration (r = 0.87; P < 0.001) and a highly significant inverse correlation with the LDL particle diameter (r = −0.74; P < 0.001). At least three highly atherogenic LDL that could be found in human plasma, namely oxidized, glycated and small-dense, are characterized by a greater electric charge. The LDL profile from capillary ITP and the relative prevalence of faster or slower migrating LDL fractions could indicate the presence of more atherogenic LDL.—Bittolo-Bon, G., and G. Cazzolato. Analytical capillary isotachophoresis of total plasma lipoproteins: a new tool to identify atherogenic low density lipoproteins. J. Lipid Res. 1999. 40: 170–177.
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spelling doaj.art-1dc1756b1b50448793c37eafb28762b02022-12-21T23:18:39ZengElsevierJournal of Lipid Research0022-22751999-01-01401170177Analytical capillary isotachophoresis of total plasma lipoproteins: a new tool to identify atherogenic low density lipoproteinsGabriele Bittolo-Bon0Giuseppe Cazzolato1To whom correspondence should be addressed.; Department of Internal Medicine and Metabolic Diseases, Pietro Avogaro Laboratory, Regional Center for Atherosclerosis, Venice General Hospital, C. po SS Giovanni e Paolo. 30122-Venice, ItalyDepartment of Internal Medicine and Metabolic Diseases, Pietro Avogaro Laboratory, Regional Center for Atherosclerosis, Venice General Hospital, C. po SS Giovanni e Paolo. 30122-Venice, ItalyPlasma low density lipoproteins from 20 patients were separated by capillary isotachophoresis (ITP). In each patient the apparent diameter of the predominant LDL peak on whole plasma was also determined by nondenaturing gradient gel electrophoresis. Furthermore the concentration of the more electronegatively charged in vivo oxidized LDL− was accomplished using anion exchange high pressure liquid chromatography. By analytical capillary ITP of whole plasma lipoproteins, prestained with a lipophilic dye, LDL were separated into four subfractions. Usually, the predominant subfraction was the slow migrating LDL4, followed by LDL3, and then by the faster LDL2 and LDL1. Slow migrating LDL4 correlated negatively with plasma triglycerides and LDL− and positively with plasma high density lipoprotein (HDL) cholesterol and with the LDL diameter, while the faster LDL1 showed an inverse behavior. The LDL1 + LDL2 to LDL3 + LDL4 ratio showed a strong positive correlation with LDL− concentration (r = 0.87; P < 0.001) and a highly significant inverse correlation with the LDL particle diameter (r = −0.74; P < 0.001). At least three highly atherogenic LDL that could be found in human plasma, namely oxidized, glycated and small-dense, are characterized by a greater electric charge. The LDL profile from capillary ITP and the relative prevalence of faster or slower migrating LDL fractions could indicate the presence of more atherogenic LDL.—Bittolo-Bon, G., and G. Cazzolato. Analytical capillary isotachophoresis of total plasma lipoproteins: a new tool to identify atherogenic low density lipoproteins. J. Lipid Res. 1999. 40: 170–177.http://www.sciencedirect.com/science/article/pii/S0022227520333538oxidized LDLLDL sizelipoprotein subfractionation
spellingShingle Gabriele Bittolo-Bon
Giuseppe Cazzolato
Analytical capillary isotachophoresis of total plasma lipoproteins: a new tool to identify atherogenic low density lipoproteins
Journal of Lipid Research
oxidized LDL
LDL size
lipoprotein subfractionation
title Analytical capillary isotachophoresis of total plasma lipoproteins: a new tool to identify atherogenic low density lipoproteins
title_full Analytical capillary isotachophoresis of total plasma lipoproteins: a new tool to identify atherogenic low density lipoproteins
title_fullStr Analytical capillary isotachophoresis of total plasma lipoproteins: a new tool to identify atherogenic low density lipoproteins
title_full_unstemmed Analytical capillary isotachophoresis of total plasma lipoproteins: a new tool to identify atherogenic low density lipoproteins
title_short Analytical capillary isotachophoresis of total plasma lipoproteins: a new tool to identify atherogenic low density lipoproteins
title_sort analytical capillary isotachophoresis of total plasma lipoproteins a new tool to identify atherogenic low density lipoproteins
topic oxidized LDL
LDL size
lipoprotein subfractionation
url http://www.sciencedirect.com/science/article/pii/S0022227520333538
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