Apo A-IV: an update on regulation and physiologic functions

被引:80
作者
Stan, S
Delvin, E
Lambert, M
Seidman, E
Levy, E
机构
[1] Univ Montreal, Hop St Justine, Res Ctr, Montreal, PQ H3T 1C5, Canada
[2] Univ Montreal, Dept Nutr, Montreal, PQ H3T 1C5, Canada
[3] Univ Montreal, Dept Biochem, Montreal, PQ H3T 1C5, Canada
[4] Univ Montreal, Dept Pediat, Montreal, PQ H3T 1C5, Canada
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS | 2003年 / 1631卷 / 02期
基金
加拿大健康研究院;
关键词
lipoprotein; atherosclerosis; food intake; nutrient; hormone;
D O I
10.1016/S1388-1981(03)00004-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Apolipoprotein (apo) A-IV, first identified 28 years ago as a plasma lipoprotein moiety; is now known to participate in the regulation of various metabolic pathways. It is synthesized primarily in the enterocytes of the small intestine during fat absorption. After entry into the bloodstream, the 46-kDa glycoprotein apo A-IV appears associated with chylomicrons, high-density lipoproteins, and in the lipoprotein-ftee fraction. It has a role in lipid absorption, transport and metabolism, and may act as a post-prandial satiety signal, an anti-oxidant and a major factor in the prevention of atherosclerosis. After summarizing and discussing these functions for reader's comprehension, the current review focuses on the regulation of apo A-IV by nutrients, biliary components, drugs, hormones and gastrointestinal peptides. The understanding of the involved mechanisms that underline apo A-IV regulation may in the long run allow us to switch on its gene, which may confer multiple beneficial effects, including the protection from atherosclerosis. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:177 / 187
页数:11
相关论文
共 141 条
[1]   INTESTINAL EXPRESSION OF HUMAN APOLIPOPROTEIN A-IV IN TRANSGENIC MICE FAILS TO INFLUENCE DIETARY-LIPID ABSORPTION OR FEEDING-BEHAVIOR [J].
AALTOSETALA, K ;
BISGAIER, CL ;
HO, A ;
KIEFT, KA ;
TRABER, MG ;
KAYDEN, HJ ;
RAMAKRISHNAN, R ;
WALSH, A ;
ESSENBURG, AD ;
BRESLOW, JL .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 93 (04) :1776-1786
[2]   DISTRIBUTION AND POSTPRANDIAL RELEASE OF PORCINE PEPTIDE-YY [J].
ADRIAN, TE ;
BACARESEHAMILTON, AJ ;
SMITH, HA ;
CHOHAN, P ;
MANOLAS, KJ ;
BLOOM, SR .
JOURNAL OF ENDOCRINOLOGY, 1987, 113 (01) :11-14
[3]   APOLIPOPROTEIN A-IV SYNTHESIS IN RAT INTESTINE - REGULATION BY DIETARY TRIGLYCERIDE [J].
APFELBAUM, TF ;
DAVIDSON, NO ;
GLICKMAN, RM .
AMERICAN JOURNAL OF PHYSIOLOGY, 1987, 252 (05) :G662-G666
[4]   THE EFFECT OF TRIIODOTHYRONINE ON RAT APOLIPOPROTEIN-A-I AND APOLIPOPROTEIN-A-IV GENE-TRANSCRIPTION [J].
APOSTOLOPOULOS, JJ ;
LASCALA, MJ ;
HOWLETT, GJ .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1988, 154 (03) :997-1002
[5]  
APOSTOLOPOULOS JJ, 1987, J LIPID RES, V28, P642
[6]  
ASAKAWA J, 1985, HUM GENET, V70, P222
[7]   ISOLATION OF A HIGH-DENSITY-LIPOPROTEIN CONVERSION FACTOR FROM HUMAN-PLASMA - A POSSIBLE ROLE OF APOLIPOPROTEIN-A-IV AS ITS ACTIVATOR [J].
BARTER, PJ ;
RAJARAM, OV ;
CHANG, LBF ;
RYE, KA ;
GAMBERT, P ;
LAGROST, L ;
EHNHOLM, C ;
FIDGE, NH .
BIOCHEMICAL JOURNAL, 1988, 254 (01) :179-184
[8]   APOLIPOPROTEIN HOMOLOG OF RAT APOLIPOPROTEIN A-IV IN HUMAN-PLASMA - ISOLATION AND PARTIAL CHARACTERIZATION [J].
BEISIEGEL, U ;
UTERMANN, G .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1979, 93 (03) :601-608
[9]   ALKYLTHIOACETIC ACID (3-THIA FATTY-ACIDS) - A NEW GROUP OF NON-BETA-OXIDIZABLE, PEROXISOME-INDUCING FATTY-ACID ANALOGS .1. A STUDY ON THE STRUCTURAL REQUIREMENTS FOR PROLIFERATION OF PEROXISOMES AND MITOCHONDRIA IN RAT-LIVER [J].
BERGE, RK ;
AARSLAND, A ;
KRYVI, H ;
BREMER, J ;
AARSAETHER, N .
BIOCHIMICA ET BIOPHYSICA ACTA, 1989, 1004 (03) :345-356
[10]   TOXICITY OF PEROXISOME PROLIFERATORS [J].
BIERI, F ;
LHUGUENOT, JC .
BIOCHIMIE, 1993, 75 (3-4) :263-268