Journal
NEUROPHARMACOLOGY
Volume 76, Issue -, Pages 51-56Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.neuropharm.2013.08.026
Keywords
beta-amyloid; Alzheimer's disease; Nerve terminal; Synaptosomes; Glutamatergic; Cholinergic
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Funding
- Fundacao para a Ciencia e Tecnologia [PTDC/SAU-NMC/114810/2009, PEst-c/SAU/LA0001/2011]
- Fundação para a Ciência e a Tecnologia [PTDC/SAU-NMC/114810/2009] Funding Source: FCT
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Alzheimer's disease (AD) is characterized phenotypically by memory impairment, neurochemically by accumulation of beta-amyloid peptide (such as A beta(1-42)) and morphologically by an initial loss of nerve terminals in cortical and hippocampal regions. However, it is not known what nerve terminals are mostly affected in early AD. We now used a mouse model of AD, based on the intra-cerebral administration of soluble A beta(1-42), that leads to memory impairment and loss of nerve terminal markers within 2 weeks, to investigate which type of hippocampal nerve terminals was mostly affected in the hippocampus. Western blot analysis revealed a decrease of the density of vesicular glutamate transporters type 1 (vGluT1, a marker of glutamatergic terminals; -20.1 +/- 3.6%) and of vesicular acetylcholine transporters (vAChT, a marker of cholinergic terminals; -27.2 +/- 0.9%) but not of vesicular GABA transporters (vGAT, a marker of GABAergic terminals) in the hippocampus of A beta-injected mice. Immunocytochemical analysis of single hippocampal nerve terminals revealed that the decrease of the density of vGluT1 reflects a reduction of the number of vGluTl-immunopositive nerve terminals (-10.6 +/- 3.6%), while no significant changes in the number of vAChT- or vGAT-immunopositive nerve terminals were observed. This pilot study shows that, in this All-based model of AD, there is an asymmetric loss of different synaptic markers with a predominant susceptibility of glutamatergic synapses. (C) 2013 Elsevier Ltd. All rights reserved.
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