Growing evidence suggests that cellular cholesterol homeostasis is causally involved in different steps leading to pathological events in the brain of Alzheimer’s Disease (AD) patients. It was previously demonstrated that the processing of the amyloid beta-peptide precursor protein (APP) is modulated by pronounced alterations in cellular cholesterol levels using statins or cholesterol extracting agents. However, a cholesterol-rich diet was found to enhance amyloid beta-peptide (Aβ) burden in the brain of transgenic mice without clearly affecting total brain cholesterol levels. Recent retrospective epidemiological studies have reported that the use of statins potentially suppresses the development of AD. Although some HMG-CoA reductase inhibitors seem to influence the central cholesterol pool in vivo, the above epidemiological findings are probably not linked to statin-induced changes in brain membrane cholesterol levels per se since not all statins active in preventing AD enter the central nervous system (CNS). Recently, we reported that different statins, regardless of their brain availability, induce alterations in cellular cholesterol distribution in the brain. Such pleiotropic, cholesterol-synthesis independent statin effects might be indirect and are possibly mediated at the blood-brain barrier (BBB) via nitric oxide (NO) or apolipoprotein E (ApoE). Aβ:amyloid beta-peptide AD:Alzheimer’s disease ApoE:apolipoprotein E APP3:amyloid beta-peptide precursor protein BBB:blood-brain barrier CHD:coronary heart disease CHOD-PAP-cholesteroloxidase-peroxidase-aminophenazon-method:phenol-method CNS:central nervous system CSF:cerebrospinal fluid DHE:dehydroergosterol ER :endoplasmatic reticulum HMG-CoA:hydroxymethylglutaryl-coenzyme A MβCD:methyl-beta-cyclodextrin NO:nitric oxide NOs:nitric oxide synthase PUFA:polyunsaturated fatty acid SMC:smooth muscle cell SPM:synaptosomal plasma membrane SUV:small unilammelar vesicle TNBS:trinitrobenzensulfonic acid