In support, AB was shown to have potent antimicrobial properties, reducing the growth of E. coli by up to 200 fold in vitro, with activity against both Gram positive and Gram negative glucose metabolism Inhibitors,Modulators,Libraries bacteria, and also against the fungus Candida albicans. In the same study, brain homogenates from AD patients showed elevated antimicrobial activity versus control homogenates. It is not yet known whether AB catalyzed sterol metabolism plays a role in this phenomenon. It is notable that reduction of AB in AD patients was associated with increased risk of infection and, in both of two large clinical trials of anti AB immunization in AD, 6% of patients developed enceph alitis of unknown origin, consistent with a potential defensive role of AB.

The role of APOE Given the role of APOE in modulating disease, by pathways that are only beginning to Inhibitors,Modulators,Libraries be understood, Robert Mahley argued that the diversification of APOE function, with three alleles prominent in the human popu lation, has been driven by infectious disease. APOE4 is probably the ancestral allele, and is most similar Inhibitors,Modulators,Libraries to homo logs in other species, and subsequent selection pres sure is thought to have led to the emergence of APOE2 and APOE3. The maintenance of multiple functionally different alleles in a population requires divergent selection for which sickle cell anemia affords the best precedent. Briefly, the hemoglobin S allele of B globin is generally deleterious, but has a protective effect against malaria infection, and therefore in malaria endemic areas the deleterious allele is maintained at high levels in the population.

This is paralleled by APOE, where APOE4 alleles are protective against some infectious diseases but increase the proliferation of other pathogens. As stated by Mahley, A cata clysmic event in human history driving the evolution of apoE4 to apoE3 to apoE2 could have been an infectious disease, such Inhibitors,Modulators,Libraries as the Great Plague, which killed 30 50% of Europeans in the 14th century, or smallpox. We have argued here that chronic immune stimula tion, leading to 25OHC production, contributes Inhibitors,Modulators,Libraries to the development of both ATH and AD. In both cases the APOE4 allele is a major risk factor, and APOE4 can be associated with an increased load of specific patho gens that have been implicated in disease processes. However, the exact mechanism is unknown. APOE4 is relatively poor at exporting cholesterols, and therefore would be expected to increase intracellu lar immunosterols, thereby diminishing the prolifera tion of immunosterol sensitive pathogens, and foster lipid droplet formation and vascular occlusion. This is http://www.selleckchem.com/products/MDV3100.html clearly an oversimplification, because 25OHC in cell culture inhibits several enveloped viruses whereas, in vivo, APOE4 increases their proliferation.