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Published in: Annals of Nuclear Medicine 10/2009

01-12-2009 | Original Article

Donepezil- and scopolamine-induced rCMRglu changes assessed by PET in conscious rhesus monkeys

Authors: Makoto Asai, Akihiko Fujikawa, Akihiro Noda, Sosuke Miyoshi, Nobuya Matsuoka, Shintaro Nishimura

Published in: Annals of Nuclear Medicine | Issue 10/2009

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Abstract

Objective

[18F]Fluoro-2-deoxyglucose positron emission tomography (FDG-PET) is a useful tool for measuring the regional cerebral metabolic rate of glucose (rCMRglu), which is an index of neuronal activity. Donepezil, an acetylcholine esterase inhibitor (AChEI), has been recommended as a treatment option for patients with Alzheimer’s disease (AD). We aimed to characterize the effects of donepezil on rCMRglu using FDG-PET in non-human primates.

Methods

We investigated the effects of administration of donepezil (500 μg/kg, i.m.), the non-selective muscarinic ACh receptor antagonist scopolamine (30 μg/kg, i.m.), and the coadministration of both drugs on the rCMRglu of conscious young rhesus monkeys.

Results

Donepezil increased the rCMRglu in all regions of interest except in the thalamus. Scopolamine treatment also increased the rCMRglu in all regions of interest except the cerebellum and thalamus. However, these effects disappeared with coadministration of the drugs.

Conclusions

This PET study showed that administration of donepezil or scopolamine alone increased the rCMRglu in conscious rhesus monkeys. We also found that the donepezil-induced increase was abolished by simultaneous administration of scopolamine, suggesting that muscarinic ACh receptor function plays an important role in the effect of donepezil.
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Metadata
Title
Donepezil- and scopolamine-induced rCMRglu changes assessed by PET in conscious rhesus monkeys
Authors
Makoto Asai
Akihiko Fujikawa
Akihiro Noda
Sosuke Miyoshi
Nobuya Matsuoka
Shintaro Nishimura
Publication date
01-12-2009
Publisher
Springer Japan
Published in
Annals of Nuclear Medicine / Issue 10/2009
Print ISSN: 0914-7187
Electronic ISSN: 1864-6433
DOI
https://doi.org/10.1007/s12149-009-0316-7

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