The LXR agonist TO901317 selectively lowers hippocampal Aβ42 and improves memory in the Tg2576 mouse model of Alzheimer's disease

Recent studies show that intracellular cholesterol levels can modulate the processing of amyloid precursor protein to A beta peptide. Moreover, cholesterol-rich apoE-containing lipoproteins may also promote A beta clearance. Agonists of the liver X receptor (LXR) transcriptionally induce genes involved in intracellular lipid efflux and transport, including apoE. Thus, LXR agonists have the potential to both inhibit APP processing and promote A beta clearance. Here we show that LXR agonist, TO901317, increased hippocampal ABCA1 and apoE and decreased A beta 42 levels in APP transgenic mice. TO901317 had no significant effects on levels of A beta 40, full length APP, or the APP processing products. Next, we examined the effects of TO901317 in the contextual fear conditioning paradigm; TO901317 completely reversed the contextual memory deficit in these mice. These data demonstrate that LXR agonists do not directly inhibit APP processing but rather facilitate the clearance of A beta 42 and may represent a novel therapeutic approach to Alzheimer's disease. (c) 2007 Elsevier Inc. All rights reserved.