Butyryl- and acetyl-cholinesterase inhibitory activities in essential oils of Salvia species and their constituents

Extracts of Salvia (sage) species have been reported to have cholinergic activities relevant to the treatment of Alzheimer's disease. A lack of information on the inhibition of the enzyme butyrylcholinesterase, also considered to be a target in the treatment of the disease, prompted this in vit...

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Published in:Phytotherapy research Vol. 18; no. 4; pp. 315 - 324
Main Authors: Savelev, S.U, Okello, E.J, Perry, E.K
Format: Journal Article
Language:English
Published: Chichester, UK John Wiley & Sons, Ltd 01-04-2004
Wiley
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Summary:Extracts of Salvia (sage) species have been reported to have cholinergic activities relevant to the treatment of Alzheimer's disease. A lack of information on the inhibition of the enzyme butyrylcholinesterase, also considered to be a target in the treatment of the disease, prompted this in vitro investigation of the essential oils of S. fruticosa, S. lavandulaefolia, S. officinalis and S. officinalis var. purpurea for anti‐butyrylcholinesterase activity. Dose‐dependent inhibition of human cholinesterases by the extracts and constituents was determined using the method of Ellman. A time dependent increase in the inhibition of butyrylcholinesterase by the oils of S. fruticosa and S. officinalis var. purpurea was evident. IC50 values decreased from 0.15 ± 0.007 and 0.14 ± 0.007 mg/mL after 5 min to 0.035 ± 0.016 and 0.06 ± 0.018 mg/mL after 90 min incubation time respectively. The slow onset of inhibition of butyrylcholinesterase was also shown by individual constituents, such as 3‐carene and β‐pinene. Analyses of the chemical composition of the oils and anti‐butyrylcholinesterase activity of their constituents revealed that none of the compounds tested would account for the total activity of the oils and that synergy is likely. Copyright © 2004 John Wiley & Sons, Ltd.
Bibliography:istex:623A68CC8FB788B4A85DEAEB20568213B67AC25E
ArticleID:PTR1451
ark:/67375/WNG-F6WTTNTH-0
ISSN:0951-418X
1099-1573
DOI:10.1002/ptr.1451