Lipoprotein profiles in plasma and interstitial fluid analyzed with an automated gel-filtration system

被引:107
作者
Parini, P [1 ]
Johansson, L [1 ]
Bröijersén, A [1 ]
Angelin, B [1 ]
Rudling, M [1 ]
机构
[1] Karolinska Univ Hosp, Karolinska Inst, Stockholm, Sweden
关键词
cholesterol; hyperglycerolaemia; interstitial fluid; lipoprotein separation; size-exclusion gel chromatography; triglycerides;
D O I
10.1111/j.1365-2362.2006.01597.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
High-quality methods for lipoprotein characterization are warranted in studies on various metabolic diseases. An automated system for size-exclusion chromatography (SEC) of lipoproteins using commercially available components is described. Cholesterol or triglyceride content in separated lipoproteins from plasma and interstitial fluid (IF) was continuously determined on-line using microlitre sample volumes. The lipoprotein assay showed a good concordance with the classic ultra-centrifugation/precipitation technique using fresh or frozen samples. Determination of lipoproteins in IF obtained from vacuum-induced skin blisters from 18 healthy subjects revealed that very low density lipoprotein (VLDL), low density lipoprotein (LDL) and high density lipoprotein (HDL) cholesterol levels were 18%, 19% and 25%, respectively, of concomitant plasma concentrations. The size-exclusion chromatography (SEC) system also allows for triglyceride determination on-line and it could be shown that the system is advantageous for an accurate determination of triglycerides in conditions when there are high levels of glycerol, e.g. in mice and in patients with hyperglycerolaemia (pseudo-hypertriglyceridaemia). The described system should be of value in studies where detailed lipoprotein analysis is warranted and particularly when significant sample series with small volumes are available. Our data also suggest that there is a 4-5.5-fold concentration gradient between plasma and IF for the three major plasma lipoproteins.
引用
收藏
页码:98 / 104
页数:7
相关论文
共 26 条
  • [1] Hepatic cholesterol metabolism and resistance to dietary cholesterol in LXRβ-deficient mice
    Alberti, S
    Schuster, G
    Parini, P
    Feltkamp, D
    Diczfalusy, U
    Rudling, M
    Angelin, B
    Björkhem, I
    Pettersson, S
    Gustafsson, JÅ
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2001, 107 (05) : 565 - 573
  • [2] Variations in lipid and apolipoprotein concentrations in human leg lymph: effects of posture and physical exercise
    Cooke, CJ
    Nanjee, MN
    Stepanova, IP
    Olszewski, WL
    Miller, NE
    [J]. ATHEROSCLEROSIS, 2004, 173 (01) : 39 - 45
  • [3] HUMAN SUCTION BLISTER INTERSTITIAL FLUID PREVENTS METAL ION-DEPENDENT OXIDATION OF LOW-DENSITY-LIPOPROTEIN BY MACROPHAGES AND IN CELL-FREE SYSTEMS
    DABBAGH, AJ
    FREI, B
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1995, 96 (04) : 1958 - 1966
  • [4] NORMAL PLASMA-LIPOPROTEINS AND FERTILITY IN GENE-TARGETED MICE HOMOZYGOUS FOR A DISRUPTION IN THE GENE ENCODING VERY-LOW-DENSITY LIPOPROTEIN RECEPTOR
    FRYKMAN, PK
    BROWN, MS
    YAMAMOTO, T
    GOLDSTEIN, JL
    HERZ, J
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (18) : 8453 - 8457
  • [5] Garber DW, 2000, J LIPID RES, V41, P1020
  • [6] ATHEROSCLEROSIS - LOW-DENSITY LIPOPROTEIN RECEPTOR HYPOTHESIS
    GOLDSTEIN, JL
    BROWN, MS
    [J]. METABOLISM-CLINICAL AND EXPERIMENTAL, 1977, 26 (11): : 1257 - 1275
  • [7] Thyroid hormone receptor β-deficient mice show complete loss of the normal cholesterol 7α-hydroxylase (CYP7A) response to thyroid hormone but display enhanced resistance to dietary cholesterol
    Gullberg, H
    Rudling, M
    Forrest, D
    Angelin, B
    Vennström, B
    [J]. MOLECULAR ENDOCRINOLOGY, 2000, 14 (11) : 1739 - 1749
  • [8] RAPID SEPARATION OF PLASMA-LIPOPROTEINS BY GEL-PERMEATION CHROMATOGRAPHY ON AGAROSE-GEL SUPEROSE-6B
    HA, YC
    BARTER, PJ
    [J]. JOURNAL OF CHROMATOGRAPHY, 1985, 341 (01): : 154 - 159
  • [9] DISTRIBUTION AND CHEMICAL COMPOSITION OF ULTRACENTRIFUGALLY SEPARATED LIPOPROTEINS IN HUMAN SERUM
    HAVEL, RJ
    EDER, HA
    BRAGDON, JH
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1955, 34 (09) : 1345 - 1353
  • [10] Innis-Whitehouse W, 1998, J LIPID RES, V39, P679