| Literature DB >> 18448072 |
Jun Inoue1, Shin-Ichi Satoh, Mariko Kita, Mayuko Nakahara, Satoshi Hachimura, Masaaki Miyata, Tomoko Nishimaki-Mogami, Ryuichiro Sato.
Abstract
LXR, PXR, and PPARalpha are members of a nuclear receptor family which regulate the expression of genes involved in lipid metabolism. Here, we show the administration of T0901317 stimulates PPARalpha gene expression in the small intestine but not in the liver of both normal and FXR-null mice. The administration of LXR specific ligand GW3965, or PXR specific ligand PCN has the same effect, indicating that ligand-dependent activation of LXR and PXR, but not FXR, is responsible for the increased gene expression of PPARalpha in the mouse small intestine.Entities:
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Year: 2008 PMID: 18448072 DOI: 10.1016/j.bbrc.2008.04.100
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575