Effect of rosiglitazone on HDL metabolism in subjects with metabolic syndrome and low HDL

被引:9
作者
Millar, John S. [1 ,3 ]
Ikewaki, Katsunori [4 ]
Bloedon, LeAnne T. [2 ]
Wolfe, Megan L. [2 ]
Szapary, Philippe O. [2 ]
Rader, Daniel J. [2 ,3 ]
机构
[1] Univ Penn, Inst Translat Res, Dept Pharmacol, Philadelphia, PA 19104 USA
[2] Univ Penn, Inst Translat Res, Dept Med, Philadelphia, PA 19104 USA
[3] Univ Penn, Inst Diabet Obes & Metab, Philadelphia, PA 19104 USA
[4] Natl Def Med Coll, Dept Internal Med, Div Antiaging, Saitama 3598513, Japan
基金
美国国家卫生研究院;
关键词
apolipoprotein A-I; stable isotope; thia-zolidinedione; lipoprotein kinetics; high density lipoprotein; CHOLESTEROL EFFLUX CAPACITY; ESTER TRANSFER PROTEIN; LIPOPROTEIN METABOLISM; GLYCEMIC CONTROL; DOUBLE-BLIND; APOA-II; TYPE-2; PIOGLITAZONE; ALPHA; CELLS;
D O I
10.1194/jlr.P008136
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
Treatment with the peroxisome proliferator-activated receptor gamma agonist rosiglitazone has been reported to increase HDL-cholesterol (HDL-C) levels, although the mechanism responsible for this is unknown. We sought to determine the effect of rosiglitazone on HDL apolipoprotein A-I (apoA-I) and apoA-II metabolism in subjects with metabolic syndrome and low HDL-C. Subjects were treated with placebo followed by rosiglitazone (8 mg) once daily. At the end of each 8 week treatment, subjects (n = 15) underwent a kinetic study to measure apoA-I and apoA-II production rate (PR) and fractional catabolic rate. Rosiglitazone significantly reduced fasting insulin and high-sensitivity C-reactive protein (hsCRP) and increased apoA-II levels. Mean apoA-I and HDL-C levels were unchanged following rosiglitazone treatment, although there was considerable individual variability in the HDL-C response. Rosiglitazone had no effect on apoA-I metabolism, whereas the apoA-II PR was increased by 23%. The change in HDL-C in response to rosiglitazone was significantly correlated with the change in apoA-II concentration but not to changes in apoA-I, measures of glucose homeostasis, or hsCRP. Treatment with rosiglitazone significantly increased apoA-II production in subjects with metabolic syndrome and low HDL-C but had no effect on apoA-I metabolism. The change in HDL-C in response to rosiglitazone treatment was unrelated to effects on apoA-I, instead being related to the change in the metabolism of apoA-II.-Millar, J. S., K. Ikewaki, L. T. Bloedon, M. L. Wolfe, P. O. Szapary, and D. J. Rader. Effect of rosiglitazone on HDL metabolism in subjects with metabolic syndrome and low HDL. J. Lipid Res. 2011. 52: 136-142.
引用
收藏
页码:136 / 142
页数:7
相关论文
共 44 条
[1]   Peroxisome proliferator-activated receptor-γ represses GLUT4 promoter activity in primary adipocytes, and rosiglitazone alleviates this effect [J].
Armoni, M ;
Kritz, N ;
Harel, C ;
Bar-Yoseph, F ;
Chen, H ;
Quon, MJ ;
Karnieli, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (33) :30614-30623
[2]   Is there a role for fibrates in the management of dyslipidemia in the metabolic syndrome? [J].
Barter, Philip J. ;
Rye, Kerry-Anne .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2008, 28 (01) :39-46
[3]   Apolipoprotein A-II is inversely associated with risk of future coronary artery disease [J].
Birjmohun, Rakesh S. ;
Dallinga-Thie, Geesje M. ;
Kuivenhoven, Jan Albert ;
Stroes, Erik S. G. ;
Otvos, James D. ;
Wareham, Nicholas J. ;
Luben, Robert ;
Kastelein, John J. P. ;
Khaw, Kay-Tee ;
Boekholdt, S. Matthijs .
CIRCULATION, 2007, 116 (18) :2029-2035
[4]  
Blanco-Vaca F, 2001, J LIPID RES, V42, P1727
[5]   Efficacy and safety of an extended-release niacin (Niaspan): A long-term study [J].
Capuzzi, DM ;
Guyton, JR ;
Morgan, JM ;
Goldberg, AC ;
Kreisberg, RA ;
Brusco, OA ;
Brody, J .
AMERICAN JOURNAL OF CARDIOLOGY, 1998, 82 (12A) :74U-81U
[6]   Rosiglitazone modifies HDL structure and increases HDL-apo AI synthesis and catabolic rates [J].
Carreon-Torres, Elizabeth ;
Rendon-Sauer, Karla ;
Monter-Garrido, Mariana ;
Toledo-Ibelles, Paola ;
Gamboa, Ricardo ;
Menjivar, Marta ;
Lopez-Marure, Rebeca ;
Luc, Gerald ;
Fievet, Catherine ;
Cruz, David ;
Vargas-Alarcon, Gilberto ;
Perez-Mendez, Oscar .
CLINICA CHIMICA ACTA, 2009, 401 (1-2) :37-41
[7]   A meta-analysis comparing the effect of thiazolidinediones on cardiovascular risk factors [J].
Chiquette, E ;
Ramirez, G ;
DeFronzo, R .
ARCHIVES OF INTERNAL MEDICINE, 2004, 164 (19) :2097-2104
[8]   SR-BI mediates cholesterol efflux via its interactions with lipid-bound ApoE. Structural mutations in SR-BI diminish cholesterol efflux [J].
Chroni, A ;
Nieland, TJF ;
Kypreos, KE ;
Krieger, M ;
Zannis, VI .
BIOCHEMISTRY, 2005, 44 (39) :13132-13143
[9]   Executive summary of the Third Report of the National Cholesterol Education Program (NCEP) expert panel on detection, evaluation, and treatment of high blood cholesterol in adults (Adult Treatment Panel III) [J].
Cleeman, JI ;
Grundy, SM ;
Becker, D ;
Clark, LT ;
Cooper, RS ;
Denke, MA ;
Howard, WJ ;
Hunninghake, DB ;
Illingworth, DR ;
Luepker, RV ;
McBride, P ;
McKenney, JM ;
Pasternak, RC ;
Stone, NJ ;
Van Horn, L ;
Brewer, HB ;
Ernst, ND ;
Gordon, D ;
Levy, D ;
Rifkind, B ;
Rossouw, JE ;
Savage, P ;
Haffner, SM ;
Orloff, DG ;
Proschan, MA ;
Schwartz, JS ;
Sempos, CT ;
Shero, ST ;
Murray, EZ .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2001, 285 (19) :2486-2497
[10]   Differential effect of glimepiride and rosiglitazone on metabolic control of type 2 diabetic patients treated with metformin: a randomized, double-blind, clinical trial [J].
Derosa, G ;
Gaddi, AV ;
Piccinni, MN ;
Salvadeo, S ;
Ciccarelli, L ;
Fogari, E ;
Ghelfi, M ;
Ferrari, I ;
Cicero, AFG .
DIABETES OBESITY & METABOLISM, 2006, 8 (02) :197-205