Impact of vitamin a on high-density lipoprotein-cholesterol and scavenger receptor class BI in the obese rat

被引:17
作者
Jeyakumar, Shantnugant M. [1 ]
Vajreswari, Ayyalasomayajula [1 ]
Giridharan, Nappan V. [1 ]
机构
[1] Natl Inst Nutr, Natl Ctr Lab Anim Sci, Dept Biochem, Hyderabad 500007, Andhra Pradesh, India
关键词
retinoids; gene expression; lipoprotein; dietary supplementation; reverse cholesterol transport;
D O I
10.1038/oby.2007.534
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Scavenger receptor class BI (SR-BI), authentic high-density lipoprotein (HDL) receptors expressed in liver, are known to play an important role in HDL-cholesterol (C) metabolism and reverse cholesterol transport. Interestingly, obese rats of WNIN/Ob strain have abnormally elevated levels of serum HDL-C compared with their lean counterparts. Based on the well-established role of SR-B1 in HDL-C metabolism, it was hypothesized that these obese rats may have an underexpression of hepatic SR-B1 receptors. In view of the significant role of vitamin A in energy expenditure and obesity, we also tested whether vitamin A supplementation can correct abnormal HDL-C metabolism. Research Methods and Procedures: To test this hypothesis, 7-month-old male lean and obese rats of WNIN/Ob strain were divided into two groups; each group was subdivided into two subgroups consisting of six lean and six obese rats and received diets containing either 2.6 or 129 mg vitamin A/kg diet for 2 months. Results: At the end, obese rats receiving normal levels of vitamin A diet showed high serum HDL-C and lower hepatic SR-BI expression levels compared with lean counterparts. Furthermore, chronic dietary vitamin A supplementation resulted in overexpression of hepatic SR-BI receptors (protein and gene) with concomitant reduction in serum HDL-C levels in obese rats. Discussion: Thus, our observations highlight the role of vitamin A in reverse cholesterol transport through up-regulation of hepatic SR-BI receptors and, thereby, HDL-C homeostasis in obese rats of WNIN/Ob strain.
引用
收藏
页码:322 / 329
页数:8
相关论文
共 36 条
[1]   The identification of intestinal scavenger receptor class B, type I (SR-BI) by expression cloning and its role in cholesterol absorption [J].
Altmann, SW ;
Davis, HR ;
Yao, XR ;
Laverty, M ;
Compton, DS ;
Zhu, LJ ;
Crona, JH ;
Caplen, MA ;
Hoos, LM ;
Tetzloff, G ;
Priestley, T ;
Burnett, DA ;
Strader, CD ;
Graziano, MP .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2002, 1580 (01) :77-93
[2]   Decreased selective uptake of high density lipoprotein cholesteryl esters in apolipoprotein E knock-out mice [J].
Arai, T ;
Rinninger, F ;
Varban, L ;
Fairchild-Huntress, V ;
Liang, CP ;
Chen, WG ;
Seo, T ;
Deckelbaum, R ;
Huszar, D ;
Tall, AR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (21) :12050-12055
[3]   Cholesterol uptake in adrenal and gonadal tissues: The SR-BI and 'selective' pathway connection [J].
Azhar, S ;
Leers-Sucheta, S ;
Reaven, E .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2003, 8 :S998-S1029
[4]   Loss of SR-BI expression leads to the early onset of occlusive atherosclerotic coronary artery disease, spontaneous myocardial infarctions, severe cardiac dysfunction, and premature death in apolipoprotein E-deficient mice [J].
Braun, A ;
Trigatti, BL ;
Post, MJ ;
Sato, K ;
Simons, M ;
Edelberg, JM ;
Rosenberg, RD ;
Schrenzel, M ;
Krieger, M .
CIRCULATION RESEARCH, 2002, 90 (03) :270-276
[5]   Lipopolysaccharide inhibits the expression of the scavenger receptor Cla-1 in human monocytes and macrophages [J].
Buechler, C ;
Ritter, M ;
Quoc, CD ;
Agildere, A ;
Schmitz, G .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 262 (01) :251-254
[6]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[7]  
DIETSCHY JM, 1993, J LIPID RES, V34, P1637
[8]  
FOLCH J, 1957, J BIOL CHEM, V226, P497
[9]  
Glomset J A, 1973, Adv Lipid Res, V11, P1
[10]   HDL-associated estradiol stimulates endothelial NO synthase and vasodilation in an SR-BI-dependent manner [J].
Gong, M ;
Wilson, M ;
Kelly, T ;
Su, W ;
Dressman, J ;
Kincer, J ;
Matveev, SV ;
Guo, L ;
Guerin, T ;
Li, XA ;
Zhu, WF ;
Uittenbogaard, A ;
Smart, EJ .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 111 (10) :1579-1587