Fat ingestion is associated with increased levels of apoC-III- and apoE-B-containing lipoprotein particles in humans

被引:10
作者
Dallongeville, J [1 ]
Baugé, E [1 ]
Lebel, P [1 ]
Fruchart, JC [1 ]
机构
[1] Inst Pasteur, Dept Atherosclerose, INSERM, U325, F-59019 Lille, France
关键词
apolipoprotein C-III; apolipoprotein E; lipid; lipoprotein; nutrition; very low-density lipoprotein;
D O I
10.1046/j.1365-2362.1997.2350782.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Apolipoprotein (ape) C-III and apoE have a major influence on post-prandial apoB-containing lipoprotein metabolism. The goal of the present study was to compare the post-prandial changes in particles containing apoB and apoC-III and those containing apoB and apoE. Twenty subjects consumed a fatty meal (1 g of fat kg(-1)). Human lipoprotein particles were measured by enzyme-linked immunosorbent assay (ELISA) using combinations of anti-apoC-III, -apoE and -apoB. Post-prandial lipaemia was associated with an increase in LpC-III:B (+100%) and LpE:B (+55%; P<0.05), which occurred 4.07 +/- 1.2 and 4.7 +/- 0.8 h after the meal respectively (P < 0.05). Cel filtration chromatography showed that fasting plasma LpC-III:B and LpE:B eluted in two fractions consisting of large and smaller sized particles; 3 h after the meal, LpC-III:B and LpE:B increased in the very low-density lipoprotein (VLDL) + intermediate-density lipoprotein (IDL) fraction; at 6 h, LpC-III:B and LpE:B decreased in VLDL and LpE:B increased moderately in the low-density lipoprotein (LDL) size range; at 10 h, both concentrations of lipoprotein particles returned to fasting levels. In conclusion, apoC-III-B-containing and apoE-B-containing lipoproteins have different post-prandial metabolic fates. These differences may result in different atherogenic potential.
引用
收藏
页码:1055 / 1060
页数:6
相关论文
共 28 条
[1]   INTERACTION OF LPB, LPB-E, LPB-C-III, AND LPB-C-III-E LIPOPROTEINS WITH THE LOW-DENSITY-LIPOPROTEIN RECEPTOR OF HELA-CELLS [J].
AGNANI, G ;
BARD, JM ;
CANDELIER, L ;
DELATTRE, S ;
FRUCHART, JC ;
CLAVEY, V .
ARTERIOSCLEROSIS AND THROMBOSIS, 1991, 11 (04) :1021-1029
[2]  
ALAUPOVIC P, 1991, ADV EXP MED BIOL, V285, P299
[3]  
ALAUPOVIC P, 1988, CLIN CHEM, V34, pB13
[4]   APOLIPOPROTEIN COMPOSITION AS THE BASIS FOR CLASSIFYING PLASMA-LIPOPROTEINS - CHARACTERIZATION OF APOA-CONTAINING AND APO-B-CONTAINING LIPOPROTEIN FAMILIES [J].
ALAUPOVIC, P .
PROGRESS IN LIPID RESEARCH, 1991, 30 (2-3) :105-138
[5]  
ALAUPOVIC P, 1992, NUTR METAB CARDIOVAS, V2, P52
[6]   PARENTAL HISTORY OF EARLY MYOCARDIAL-INFARCTION IS ASSOCIATED WITH DECREASED LEVELS OF LIPOPARTICLE-AI IN ADOLESCENTS [J].
AMOUYEL, P ;
ISOREZ, D ;
BARD, JM ;
GOLDMAN, M ;
LEBEL, P ;
ZYLBERBERG, G ;
FRUCHART, JC .
ARTERIOSCLEROSIS AND THROMBOSIS, 1993, 13 (11) :1640-1644
[7]   ISOLATION AND CHARACTERIZATION OF 2 SUBSPECIES OF LP(A), ONE CONTAINING APO-E AND ONE FREE OF APO-E [J].
BARD, JM ;
DELATTRELESTAVEL, S ;
CLAVEY, V ;
PONT, P ;
DERUDAS, B ;
PARRA, HJ ;
FRUCHART, JC .
BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1127 (02) :124-130
[8]   ISOLATION AND CHARACTERIZATION OF HUMAN LP-B LIPOPROTEIN CONTAINING APOLIPOPROTEIN-B AS THE SOLE APOLIPOPROTEIN [J].
BARD, JM ;
CANDELIER, L ;
AGNANI, G ;
CLAVEY, V ;
TORPIER, G ;
STEINMETZ, A ;
FRUCHART, JC .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1082 (02) :170-176
[9]   PREDICTION OF ANGIOGRAPHIC CHANGE IN NATIVE HUMAN CORONARY-ARTERIES AND AORTOCORONARY BYPASS GRAFTS - LIPID AND NONLIPID FACTORS [J].
BLANKENHORN, DH ;
ALAUPOVIC, P ;
WICKHAM, E ;
CHIN, HP ;
AZEN, SP .
CIRCULATION, 1990, 81 (02) :470-476
[10]   MODULATION OF LIPOPROTEIN B BINDING TO THE LDL RECEPTOR BY EXOGENOUS LIPIDS AND APOLIPOPROTEIN-CI, APOLIPOPROTEIN-CII, APOLIPOPROTEIN-CIII, AND APOLIPOPROTEIN-E [J].
CLAVEY, V ;
LESTAVELDELATTRE, S ;
COPIN, C ;
BARD, JM ;
FRUCHART, JC .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1995, 15 (07) :963-971