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Papers In Press, published online ahead of print August 16, 2003
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Discovery Research, CV Therapeutics, Palo Alto, CA 94304
Corresponding Author: jeffrey.chisholm{at}cvt.com
Liver-X-receptor (LXR) ligands are currently being evaluated as potential therapeutic agents for the treatment of low HDL. The LXR ligand T0901317 elevates ATP-binding cassette A1 (ABCA1) and HDL levels in animal models and induces moderate lipogenesis through upregulation of sterol regulatory element binding protein 1c (SREBP1c). Since insulin may also regulate lipogenesis through SREBP1c and fatty acid synthase (FAS) we investigated the effect of an LXR ligand in hyperinsulinemic mice. Administration of T0901317 to male DB/DB mice for 12 days resulted in a more severe hypertriacylglycerolemia and hepatic triacylglycerol accumulation than observed in non-diabetic mice. The LXR target genes ABCA1, SREBP1c, FAS, stearoyl CoA desaturase 1 (SCD1) were upregulated by T0901317 treatment in both diabetic DB/DB and non-diabetic C57BLKS mice. Changes in lipogenic gene expression were independent of mouse strain indicating that the severe lipogenesis observed in LXR ligand treated DB/DB mice was not due to additive effects of insulin on lipogenic gene expression. Phosphoenolpyruvate carboxykinase expression was suppressed suggesting that a shift from gluconeogenesis towards lipogenesis could partially explain our observations in DB/DB mice. Our data suggest that LXR ligands that have effects on both fatty acid and carbohydrate metabolism should be carefully evaluated in obesity, insulin and leptin resistance.
Revised on August 8, 2003
Accepted on August 8, 2003
The LXR ligand T0901317 induces severe lipogenesis in the DB/DB diabetic mouse
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