MBX-102/JNJ39659100, a Novel Non-TZD Selective Partial PPAR-γ Agonist Lowers Triglyceride Independently of PPAR-α Activation

被引:15
作者
Chandalia, Apurva [1 ]
Clarke, Holly J. [1 ,2 ]
Clemens, L. Edward [1 ]
Pandey, Bindu [1 ]
Vicena, Vic [1 ]
Lee, Paul [1 ]
Lavan, Brian E. [1 ]
Gregoire, Francine M. [1 ]
机构
[1] Metabolex Inc, Dept Biol, Hayward, CA 94545 USA
[2] Genentech Inc, Dept Mol Biol, San Francisco, CA 94080 USA
关键词
HALOFENATE; PIOGLITAZONE; MECHANISM; ROSIGLITAZONE; CLOFIBRATE; DELTA; BONE; RECEPTORS; MODULATOR; EFFICACY;
D O I
10.1155/2009/706852
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
MBX-102/JNJ-39659100 (MBX-102) is a selective, partial PPAR-gamma agonist that lowers glucose in the absence of some of the side effects, such as weight gain and edema, that are observed with the TZDs. Interestingly MBX-102 also displays pronounced triglyceride lowering in preclinical rodent models and in humans. Although in vitro reporter gene studies indicated that MBX-102 acid is a highly selective PPAR-gamma agonist that lacks PPAR-alpha activity, we sought to determine if PPAR-a activation in vivo could possibly contribute to the triglyceride lowering abilities of MBX-102. In vivo studies using ZDF and ZF rats demonstrated that MBX-102 lowered plasma triglycerides. However in ZF rats, MBX-102 had no effect on liver weight or on hepatic expression levels of PPAR-alpha target genes. Further in vitro studies in primary human hepatocytes supported these findings. Finally, the ability of MBX-102 to lower triglycerides was maintained in PPAR-alpha knockout mice, unambiguously establishing that the triglyceride lowering effect of MBX-102 is PPAR-alpha independent. The in vivo lipid lowering abilities of MBX-102 are therefore mediated by an alternate mechanism which is yet to be determined.
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页数:12
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