Protecting Synaptic Connectivity in Alzheimer's Disease

Grant number: 1100324 | Funding period: 2016 - 2024

Completed

Abstract

In Alzheimer’s disease, connections between neurons (synapses) are progressively damaged. The BACE inhibitor class of drugs entering Phase III clinical trials may slow the pace of neurodegeneration in patients with dementia. However, these drugs may simultaneously have negative effects on synapse function, learning and memory. This study will assess the effect of BACE inhibition on synapse properties and cognition and identify the contribution of key proteins affected by this treatment.

Related publications (2)

Functions of the Alzheimer’s Disease Protease BACE1 at the Synapse in the Central Nervous System

KM Munro, A Nash, M Pigoni, SF Lichtenthaler, JM Gunnersen

2016-11-01

Inhibition of the protease β-site amyloid precursor protein-cleaving enzyme 1 (BACE1) is a promising treatment strategy for Alzhei..

Seizure protein 6 and its homolog seizure 6-like protein are physiological substrates of BACE1 in neurons

M Pigoni, J Wanngren, PH Kuhn, KM Munro, JM Gunnersen, H Takeshima, R Feederle, I Voytyuk, B De Strooper, MD Levasseur, BJ Hrupka, SA Müller, SF Lichtenthaler

2016-01-01

Background: The protease BACE1 (beta-site APP cleaving enzyme) is a major drug target in Alzheimer's disease. However, BACE1 thera..

University of Melbourne Researchers

Kathryn Munro