Correlation Engine 2.0
Clear Search sequence regions

The efficient clearance of amyloid-β (Aβ) is essential to modulate levels of the peptide in the brain and to prevent it from accumulating in senile plaques, a hallmark of Alzheimer's disease (AD) pathology.We and others have shown that failure in catabolism can produce elevations in concentration similar to those observed in familial forms of AD. Based on the available evidence, it remains plausible that in late-onset AD, disturbances in the activity of degrading enzymes could induce accumulation, and that this increase could result in AD pathology. The following review presents a historical perspective of the parallel discovery of three vasopeptidases (neprilysin and endothelin-converting enzymes-1 and -2) as important degrading enzymes. The recognition of the role of these vasopeptidases in degradation, beyond bringing to light a possible explanation of how cardiovascular risk factors may influence AD risk, highlights a possible risk of the use of inhibitors of these enzymes for other clinical indications such as hypertension. We will discuss in detail the experiments conducted to assess the impact of vasopeptidase deficiency (through pharmacological inhibition or genetic mutation) on accumulation, as well as the cooperative effect of multiple degrading enzymes to regulate the concentration of the peptide at multiple sites, both intracellular and extracellular, throughout the brain.


Javier Pacheco-Quinto, Aimee Herdt, Christopher B Eckman, Elizabeth A Eckman. Endothelin-converting enzymes and related metalloproteases in Alzheimer's disease. Journal of Alzheimer's disease : JAD. 2013;33 Suppl 1:S101-10

Expand section icon Mesh Tags

Expand section icon Substances

PMID: 22903130

View Full Text