Journal
BRAIN
Volume 137, Issue -, Pages 553-564Publisher
OXFORD UNIV PRESS
DOI: 10.1093/brain/awt308
Keywords
Alzheimer's disease; peripheral sink hypothesis; amyloid-beta; neprilysin
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Funding
- MedImmune Ltd
- AstraZeneca RD
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Alzheimer's disease is characterized by the accumulation of amyloid deposits in the brain and the progressive loss of cognitive functions. Although the precise role of amyloid-beta in disease progression remains somewhat controversial, many efforts to halt or reverse disease progression have focussed on reducing its synthesis or enhancing its removal. It is believed that brain and peripheral soluble amyloid-beta are in equilibrium and it has previously been hypothesized that a reduction in peripheral amyloid-beta can lower brain amyloid-beta, thereby reducing formation of plaques predominantly composed of insoluble amyloid-beta; the so-called peripheral sink hypothesis. Here we describe the use of an amyloid-beta degrading enzyme, the endogenous metallopeptidase neprilysin, which is fused to albumin to extend plasma half-life and has been engineered to confer increased amyloid-beta degradation activity. We used this molecule to investigate the effect of degradation of peripheral amyloid-beta on amyloid-beta levels in the brain and cerebrospinal fluid after repeated intravenous dosing for up to 4 months in Tg2576 transgenic mice, and 1 month in rats and monkeys. This molecule proved highly effective at degradation of amyloid-beta in the periphery but did not alter brain or cerebrospinal fluid amyloid-beta levels, suggesting that the peripheral sink hypothesis is not valid and is the first time that this has been demonstrated in non-human primates.
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