Moderately Decreased Cholesterol Absorption Rates Are Associated With a Large Atheroprotective Effect

被引:20
作者
Greenberg, Michael E. [1 ]
Smith, Jonathan D. [2 ]
Sehayek, Ephraim [1 ]
机构
[1] Cleveland Clin, Inst Genom Med, Lerner Res Inst, Cleveland, OH USA
[2] Cleveland Clin, Dept Cell Biol, Lerner Res Inst, Cleveland, OH USA
关键词
cholesterol; absorption; atherosclerosis; reverse cholesterol transport; macrophage; KNOCKOUT MICE; ATHEROSCLEROSIS; EZETIMIBE; MACROPHAGES; SIMVASTATIN; INHIBITOR; EXCRETION;
D O I
10.1161/ATVBAHA.109.194605
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective-Human treatment with ezetimibe results in a moderate 50% to 54% decrease in cholesterol absorption and a 15% to 20% decrease in plasma LDL-cholesterol levels; nevertheless, the efficacy of ezetimibe therapy has been recently challenged by the ENHANCE trial. We examined the efficacy of a moderate decrease in cholesterol absorption in preventing atherosclerosis formation in the mouse. Methods and Results-Congenic 14DKK animals, consisting of a castaneus (CASA/Rk) chromosome 14 interval introgressed onto the C57BL/6J background, displayed a moderate decrease in cholesterol absorption rates. The effect of moderately decreased absorption on atherosclerosis formation was determined in 14DKK apolipoprotein E knockouts (14DKK-apoEKO). When compared to chow diet-fed control apoEKO mice, congenic 14DKK-apoEKO displayed a moderate 41% decrease in cholesterol absorption rates, 30% to 37% decrease in plasma cholesterol levels, and a 70% decrease in atherosclerosis formation. Studies on cholesterol efflux and reverse cholesterol transport (RCT) from 14DKK bone marrow-derived macrophages rejected a 14DKK interval-dependent atheroprotective effects that operate in macrophages. In contrast, 14DKK-apoEKO congenics were characterized by a 60% increase in RCT from peripheral tissue macrophages. Conclusions-These studies strongly suggest that moderately decreased cholesterol absorption rates result in a large atheroprotective effect attributable to a decrease in plasma cholesterol levels and an increase in RCT from peripheral tissue macrophages. (Arterioscler Thromb Vasc Biol. 2009; 29: 1745-1750.)
引用
收藏
页码:1745 / 1750
页数:6
相关论文
共 19 条
[1]   Cholesterol absorption inhibitors: Defining new options in lipid management [J].
Brown, WV .
CLINICAL CARDIOLOGY, 2003, 26 (06) :259-264
[2]   Rationale and design of IMPROVE-IT (IMProved Reduction of Outcomes: Vytorin Efficacy International Trial): Comparison of ezetimbe/simvastatin versus simvastatin monotherapy on cardiovascular outcomes in patients with acute coronary syndromes [J].
Cannon, Christopher P. ;
Giugliano, Robert P. ;
Blazing, Michael A. ;
Harrington, Robert A. ;
Peterson, John L. ;
Sisk, Christine McCrary ;
Strony, John ;
Musliner, Thomas A. ;
McCabe, Carolyn H. ;
Veltri, Enrico ;
Braunwald, Eugene ;
Califf, Robert M. .
AMERICAN HEART JOURNAL, 2008, 156 (05) :826-832
[3]   Genetic background determines the extent of atherosclerosis in ApoE-deficient mice [J].
Dansky, HM ;
Charlton, SA ;
Sikes, JL ;
Heath, SC ;
Simantov, R ;
Levin, LF ;
Shu, P ;
Moore, KJ ;
Breslow, JL ;
Smith, JD .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1999, 19 (08) :1960-1968
[4]   Deficiency of Niemann-Pick C1 like 1 prevents atherosclerosis in ApoE-/- mice [J].
Davis, Harry R., Jr. ;
Hoos, Lizbeth M. ;
Tetzloff, Glen ;
Maguire, Maureen ;
Zhu, Li-ji ;
Graziano, Michael P. ;
Altmann, Scott W. .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2007, 27 (04) :841-849
[5]   Ezetimibe, a potent cholesterol absorption inhibitor, inhibits the development of atherosclerosis in ApoE knockout mice [J].
Davis, HR ;
Compton, DS ;
Hoos, L ;
Tetzloff, G .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2001, 21 (12) :2032-2038
[6]   The cholesterol absorption inhibitor ezetimibe acts by blocking the sterol-induced internalization of NPC1L1 [J].
Ge, Liang ;
Wang, Jing ;
Qi, Wei ;
Miao, Hong-Hua ;
Cao, Jian ;
Qu, Yu-Xiu ;
Li, Bo-Liang ;
Song, Bao-Liang .
CELL METABOLISM, 2008, 7 (06) :508-519
[7]   PREPARATION AND CHARACTERIZATION OF HUMAN-BONE MARROW-DERIVED MACROPHAGES [J].
HUME, DA ;
ALLAN, W ;
GOLDER, J ;
STEPHENS, RW ;
DOE, WF ;
WARREN, HS .
JOURNAL OF LEUKOCYTE BIOLOGY, 1985, 38 (04) :541-552
[8]   Simvastatin with or without ezetimibe in familial hypercholesterolemia [J].
Kastelein, John J. P. ;
Akdim, Fatima ;
Stroes, Erik S. G. ;
Zwinderman, Aeilko H. ;
Bots, Michiel L. ;
Stalenhoef, Anton F. H. ;
Visseren, Frank L. J. ;
Sijbrands, Eric J. G. ;
Trip, Mieke D. ;
Stein, Evan A. ;
Gaudet, Daniel ;
Duivenvoorden, Raphael ;
Veltri, Enrico P. ;
Marais, A. David ;
de Groot, Eric .
NEW ENGLAND JOURNAL OF MEDICINE, 2008, 358 (14) :1431-1443
[9]   Analyses of cancer data from three Ezetimibe trials [J].
Peto, Richard ;
Emberson, Jonathan ;
Landray, Martin ;
Baigent, Colin ;
Collins, Rory ;
Clare, Robert ;
Califf, Robert .
NEW ENGLAND JOURNAL OF MEDICINE, 2008, 359 (13) :1357-1366
[10]   Biliary cholesterol excretion: A novel mechanism that regulates dietary cholesterol absorption [J].
Sehayek, E ;
Ono, JG ;
Shefer, S ;
Nguyen, LB ;
Wang, N ;
Batta, AK ;
Salen, G ;
Smith, JD ;
Tall, AR ;
Breslow, JL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (17) :10194-10199