Given the absence of a major detrimental effect of the selleck chemicals knockout of the BACE1 gene, inhibition of BACE1 appears unlikely to result in severe side effects (but see ref 25). It is important to emphasize that success with BACE1 inhibitors will be dependent, to a large extent, on the validity of the

“toxic gain of function” model, as suppression of BACE1 activity seems certain to reduce rates of production of β-amyloid by Inhibitors,research,lifescience,medical reducing rates of cleavage of APP. The challenge here is that if most mutations in APP and presenilin 1 also result in reduced rates of cleavage, and produce disease by this mechanism, one would expect an acceleration of disease progression on inhibition of either BACE1 (or γ secretase Inhibitors,research,lifescience,medical – see below). One of the most significant problems here is the absence of appropriate animal models.

As mentioned above, mice with extensive amyloid deposition driven by overexpression of a mutant human APP gene do not develop a significant neurodegeneration. Thus while studies with BACE1 inhibitors could readily be performed in these mice to show reductions in amyloid deposition, few of the other features of Alzheimer’s disease are evident in these mice, so that the Inhibitors,research,lifescience,medical effects of these compounds on the pathology and/or clinical features of Alzheimer’s disease will remain untested until human trials are conducted. Use of inhibitors of γ secretase The problems with the use of γ secretase inhibitors are somewhat similar to those of inhibiting BACE1, although there are some notable distinctions. Knockout of vital components of γ secretase (presenilin 1, for example) does not produce viable mice unless the knockout is conditional26 (effectively unless the knockout is engineered to Inhibitors,research,lifescience,medical occur only in adult mice). The problem here is that γ secretase cleaves numerous proteins as well as APP, and

at least some of these proteins (eg, Notch127) play critical roles in brain development. Their role in the adult animal is less clear, although Inhibitors,research,lifescience,medical knockout of both presenilins 1 and 2 in adult animals results in a striking neurodegeneration.28,29 However, complete inhibition of y secretase is not what is intended by chemical information therapeutics, and the question still remains about whether the production of β-amyloid can be reduced without unacceptable consequences, these resulting presumably from reductions in the rate of processing of other γ secretase substrates. Preliminary reports appear to suggest that this is possible,30,31 Entinostat and it appears that a large-scale phase 3 clinical trial of a γ secretase inhibitor is now underway. Again, success would seem to be dependent largely on the validity of the “toxic gain of function” model. There is perhaps the more direct concern here that again, the treatment exacerbates rather than interrupts the disease as reductions and not increases in the activity of γ secretase appear to result from mutations, particularly in presenilin 1.