A Selective Peroxisome Proliferator-Activated Receptor α Agonist, CP-900691, Improves Plasma Lipids, Lipoproteins, and Glycemic Control in Diabetic Monkeys

被引:25
作者
Wagner, Janice D. [1 ]
Shadoan, Melanie K. [1 ]
Zhang, Li [1 ]
Ward, Gina M. [1 ]
Royer, Lori J. [3 ]
Kavanagh, Kylie [1 ]
Francone, Omar L. [3 ]
Auerbach, Bruce J. [2 ]
Harwood, H. James, Jr. [3 ]
机构
[1] Wake Forest Univ, Dept Pathol, Winston Salem, NC 27157 USA
[2] Pfizer Global Res & Dev, Dept Cardiovasc Metab & Endocrine Dis, Ann Arbor, MI USA
[3] Pfizer Global Res & Dev, Dept Cardiovasc Metab & Endocrine Dis, Groton, CT USA
关键词
EXPERIMENTAL-ANIMALS; CYNOMOLGUS MONKEYS; PPAR-GAMMA; ATHEROSCLEROSIS; DISEASE; TRIGLYCERIDES; ADIPONECTIN; CHOLESTEROL; FENOFIBRATE; PARAMETERS;
D O I
10.1124/jpet.110.166736
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Peroxisome proliferator-activated receptors (PPARs) are involved in the regulation of lipid and glucose metabolism. PPAR gamma agonists improve insulin sensitivity and hyperglycemia and are effective in treating type 2 diabetes mellitus (T2DM), whereas PPAR alpha agonists are used to treat dyslipidemia and atherosclerosis. The goal here was to examine the efficacy of a selective PPAR alpha agonist {(S)-3-[3-(1-carboxy-1-methyl-ethoxy)-phenyl]-piperidine-1-carboxylic acid 4-trifluoromethyl-benzyl ester; CP-900691} on lipid, glycemic, and inflammation indices in 14 cynomolgus monkeys with spontaneous T2DM maintained on daily insulin therapy. Monkeys were dosed orally with either vehicle (n = 7) or CP-900691 (3 mg/kg, n = 7) daily for 6 weeks. CP-900691 treatment increased plasma high-density lipoprotein cholesterol (HDLC) (33 +/- 3 to 60 +/- 4 mg/dL, p < 0.001) and apolipoprotein A1 (96 +/- 5 to 157 +/- 5 mg/dL, p < 0.001), reduced plasma triglycerides (547 +/- 102 to 356 +/- 90 mg/dL, p < 0.01), and apolipoprotein B (62 +/- 3 to 45 +/- 3 mg/dL, p < 0.01), improved the lipoprotein index (HDL to non-HDLC ratio; 0.28 +/- 0.06 to 0.79 +/- 0.16, p < 0.001), decreased body weight (p < 0.01) and C-reactive protein (CRP) (1700 +/- 382 to 304 +/- 102 ng/ml, p < 0.01), and increased adiponectin (1697 +/- 542 to 4242 +/- 1070 ng/ml, p < 0.001) compared with baseline. CP-900691 treatment reduced exogenous insulin requirements by approximately 25% (p < 0.04) while lowering plasma fructosamine from 2.87 +/- 0.09 to 2.22 +/- 0.17 mM (p < 0.05), indicative of improved glycemic control. There were no changes in any of the aforementioned parameters in the vehicle group. Because low HDLC and high triglycerides are well established risk factors for cardiovascular disease, the marked improvements in these parameters, and in glycemic control, body weight, and CRP, suggest that CP-900691 may be of benefit in diabetic and obese or hyperlipidemic populations.
引用
收藏
页码:844 / 853
页数:10
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