Improved efficacy for ezetimibe and rosuvastatin by attenuating the induction of PCSK9

被引:42
作者
Ason, Brandon [1 ]
Tep, Samnang [1 ]
Davis, Harry R., Jr. [2 ]
Xu, Yiming [2 ]
Tetzloff, Glen [2 ]
Galinski, Beverly [1 ]
Soriano, Ferdie [1 ]
Dubinina, Natalya [1 ]
Zhu, Lei [3 ]
Stefanni, Alice [2 ]
Wong, Kenny K. [2 ]
Tadin-Strapps, Marija [1 ]
Bartz, Steven R. [1 ]
Hubbard, Brian [2 ]
Ranalletta, Mollie [2 ]
Sachs, Alan B. [1 ]
Flanagan, W. Michael [1 ]
Strack, Alison [2 ]
Kuklin, Nelly A. [1 ]
机构
[1] Merck & Co Inc, Sirna Therapeut, San Francisco, CA 94158 USA
[2] Merck Res Labs, Cardiovasc & Metab Dis Res, Rahway, NJ 07065 USA
[3] Merck Res Labs, Genet Engn Models, Rahway, NJ 07065 USA
关键词
cholesterol/metabolism; drug therapy; gene expression; CHOLESTEROL ABSORPTION INHIBITOR; LOW-DENSITY-LIPOPROTEINS; COENZYME-A REDUCTASE; INTERPRETIVE HISTORY; 3-HYDROXY-3-METHYLGLUTARYL COENZYME; PLASMA-CHOLESTEROL; LDL CHOLESTEROL; MICE; ATORVASTATIN; SIMVASTATIN;
D O I
10.1194/jlr.M013664
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Reducing circulating LDL-cholesterol (LDL-c) reduces the risk of cardiovascular disease in people with hypercholesterolemia. Current approaches to reduce circulating LDL-c include statins, which inhibit cholesterol synthesis, and ezetimibe, which blocks cholesterol absorption. Both elevate serum PCSK9 protein levels in patients, which could attenuate their efficacy by reducing the amount of cholesterol cleared from circulation. To determine whether PCSK9 inhibition could enhance LDL-c lowering of both statins and ezetimibe, we utilized small interfering RNAs (siRNAs) to knock down Pcsk9, together with ezetimibe, rosuvastatin, and an ezetimibe/rosuvastatin combination in a mouse model with a human-like lipid profile. We found that ezetimibe, rosuvastatin, and ezetimibe/rosuvastatin combined lower serum cholesterol but induce the expression of Pcsk9 as well as the Srebp-2 hepatic cholesterol biosynthesis pathway. Pcsk9 knockdown in combination with either treatment led to greater reductions in serum non-HDL with a near-uniform reduction of all LDL-c subfractions. In addition to reducing serum cholesterol, the combined rosuvastatin/ezetimibe/Pcsk9 siRNA treatment exhibited a significant reduction in serum APOB protein and triglyceride levels.jlr Taken together, these data provide evidence that PCSK9 inhibitors, in combination with current therapies, have the potential to achieve greater reductions in both serum cholesterol and triglycerides.-Ason, B., S. Tep, H. R. Davis, Jr., Y. Xu, G. Tetzloff, B. Galinski, F. Soriano, N. Dubinina, L. Zhu, A. Stefanni, K. K. Wong, M. Tadin-Strapps, S. R. Bartz, B. Hubbard, M. Ranalletta, A. B. Sachs, W. M. Flanagan, A. Strack, and N. A. Kuklin. Improved efficacy for ezetimibe and rosuvastatin by attenuating the induction of PCSK9. J. Lipid Res. 2011. 52: 679-687.
引用
收藏
页码:679 / 687
页数:9
相关论文
共 61 条
[1]
Niemann-Pick C1 like 1 protein is critical for intestinal cholesterol absorption [J].
Altmann, SW ;
Davis, HR ;
Zhu, LJ ;
Yao, XR ;
Hoos, LM ;
Tetzloff, G ;
Iyer, SPN ;
Maguire, M ;
Golovko, A ;
Zeng, M ;
Wang, LQ ;
Murgolo, N ;
Graziano, MP .
SCIENCE, 2004, 303 (5661) :1201-1204
[2]
Hypertriglyceridemia as a cardiovascular risk factor [J].
Austin, MA ;
Hokanson, JE ;
Edwards, KL .
AMERICAN JOURNAL OF CARDIOLOGY, 1998, 81 (4A) :7B-12B
[3]
Ezetimibe alone or in combination with simvastatin increases small dense low-density lipoproteins in healthy men: a randomized trial [J].
Berneis, Kaspar ;
Rizzo, Manfredi ;
Berthold, Heiner K. ;
Spinas, Giatgen A. ;
Krone, Wilhelm ;
Gouni-Berthold, Ioanna .
EUROPEAN HEART JOURNAL, 2010, 31 (13) :1633-U46
[4]
BURRIER RE, 1995, J PHARMACOL EXP THER, V272, P156
[5]
Atorvastatin increases human serum levels of proprotein convertase subtilisin/kexin type 9 [J].
Careskey, Holly E. ;
Davis, R. Aleks ;
Alborn, William E. ;
Troutt, Jason S. ;
Cao, Guoqing ;
Konrad, Robert J. .
JOURNAL OF LIPID RESEARCH, 2008, 49 (02) :394-398
[6]
Phenotype-dependent and -independent actions of rosuvastatin on atherogenic lipoprotein subfractions in hyperlipidaemia [J].
Caslake, MJ ;
Stewart, G ;
Day, SP ;
Daly, E ;
McTaggart, F ;
Chapman, MJ ;
Durrington, P ;
Laggner, P ;
Mackness, M ;
Pears, J ;
Packard, CJ .
ATHEROSCLEROSIS, 2003, 171 (02) :245-253
[7]
A proprotein convertase subtilisin/kexin type 9 neutralizing antibody reduces serum cholesterol in mice and nonhuman primates [J].
Chan, Joyce C. Y. ;
Piper, Derek E. ;
Cao, Qiong ;
Liu, Dongming ;
King, Chadwick ;
Wang, Wei ;
Tang, Jie ;
Liu, Qiang ;
Higbee, Jared ;
Xia, Zhen ;
Di, Yongmei ;
Shetterly, Susan ;
Arimura, Ziva ;
Salomonis, Heather ;
Romanow, William G. ;
Thibault, Stephen T. ;
Zhang, Richard ;
Cao, Ping ;
Yang, Xiao-Ping ;
Yu, Timothy ;
Lu, Mei ;
Retter, Marc W. ;
Kwon, Gayle ;
Henne, Kirk ;
Pan, Oscar ;
Tsai, Mei-Mei ;
Fuchslocher, Bryna ;
Yang, Evelyn ;
Zhou, Lei ;
Lee, Ki Jeong ;
Daris, Mark ;
Sheng, Jackie ;
Wang, Yan ;
Shen, Wenyan D. ;
Yeh, Wen-Chen ;
Emery, Maurice ;
Walker, Nigel P. C. ;
Shan, Bei ;
Schwarz, Margrit ;
Jackson, Simon M. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (24) :9820-9825
[8]
Sequence variations in PCSK9, low LDL, and protection against coronary heart disease [J].
Cohen, JC ;
Boerwinkle, E ;
Mosley, TH ;
Hobbs, HH .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 354 (12) :1264-1272
[9]
CORESH J, 1993, J LIPID RES, V34, P1687
[10]
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