The Pharmacology of LXR

Laura   F.   Michael; Jeffrey   M.   Schkeryantz; Thomas   P.   Burris

doi:10.2174/1389557054553767

Abstract

Liver X receptors (LXRs) are members of the nuclear hormone receptor superfamily of ligandactivated transcription factors. Two LXRs (LXRa and LXRb) were initially characterized as orphan members of this superfamily with disparate patterns of tissue expression. These two receptors later were recognized as sterol-responsive with the ability to directly bind several oxysterol metabolites. Many LXR target genes have been identified that implicate these receptors in a variety of physiological processes including cholesterol transport and metabolism, glucose metabolism, and inflammation. Synthetic LXR ligands have been designed with the potential to treat disorders such as atherosclerosis and diabetes. In this review, we describe the potential utility of LXR ligands in the treatment of disease.

Keywords: nuclear receptor, steroid, hdl, ldl, transcription, heart disease, diabetes, inflammation