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Protective effect of the ethanol extract of Magnolia officinalis and 4-O-methylhonokiol on scopolamine-induced memory impairment and the inhibition of acetylcholinesterase activity

Magnolol, honokiol, and obovatol are well-known bioactive constituents of the bark of Magnolia officinalis and have been used as traditional Chinese medicines for the treatment of neurosis, anxiety, and stroke. We recently isolated novel active compound (named 4-O-methylhonokiol) from the ethanol ex...

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Autores principales: Lee, Yong Kyung, Yuk, Dong Yeon, Kim, Tae Il, Kim, Young Heui, Kim, Kyoung Tae, Kim, Ki Ho, Lee, Beom Jun, Nam, Sang-Yoon, Hong, Jin Tae
Formato: Texto
Lenguaje:English
Publicado: Springer Japan 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2690856/
https://www.ncbi.nlm.nih.gov/pubmed/19343477
http://dx.doi.org/10.1007/s11418-009-0330-z
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author Lee, Yong Kyung
Yuk, Dong Yeon
Kim, Tae Il
Kim, Young Heui
Kim, Kyoung Tae
Kim, Ki Ho
Lee, Beom Jun
Nam, Sang-Yoon
Hong, Jin Tae
author_facet Lee, Yong Kyung
Yuk, Dong Yeon
Kim, Tae Il
Kim, Young Heui
Kim, Kyoung Tae
Kim, Ki Ho
Lee, Beom Jun
Nam, Sang-Yoon
Hong, Jin Tae
author_sort Lee, Yong Kyung
collection PubMed
description Magnolol, honokiol, and obovatol are well-known bioactive constituents of the bark of Magnolia officinalis and have been used as traditional Chinese medicines for the treatment of neurosis, anxiety, and stroke. We recently isolated novel active compound (named 4-O-methylhonokiol) from the ethanol extract of Magnolia officinalis. The present study aimed to test two different doses of ethanol extracts of Magnolia officinalis (5 and 10 mg/kg/mouse, p.o., 1 week) and 4-O-methylhonokiol (0.75 and 1.5 mg/kg/mouse, p.o., 1 week) administered for 7 days on memory impairment induced by scopolamine (1 mg/kg body weight i.p.) in mice. Memory and learning were evaluated using the Morris water maze and the step-down avoidance test. Both the ethanol extract of Magnolia officinalis and 4-O-methylhonokiol prevented memory impairment induced by scopolamine in a dose-dependent manner. The ethanol extract of Magnolia officinalis and 4-O-methylhonokiol also dose-dependently attenuated the scopolamine-induced increase of acetylcholinesterase (AChE) activity in the cortex and hippocampus of mice, and inhibited AChE activity in vitro with IC(50) (12 nM). This study, therefore, suggests that the ethanol extract of Magnolia officinalis and its major ingredient, 4-O-methylhonokiol, may be useful for the prevention of the development or progression of AD.
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spelling pubmed-26908562009-06-05 Protective effect of the ethanol extract of Magnolia officinalis and 4-O-methylhonokiol on scopolamine-induced memory impairment and the inhibition of acetylcholinesterase activity Lee, Yong Kyung Yuk, Dong Yeon Kim, Tae Il Kim, Young Heui Kim, Kyoung Tae Kim, Ki Ho Lee, Beom Jun Nam, Sang-Yoon Hong, Jin Tae J Nat Med Original Paper Magnolol, honokiol, and obovatol are well-known bioactive constituents of the bark of Magnolia officinalis and have been used as traditional Chinese medicines for the treatment of neurosis, anxiety, and stroke. We recently isolated novel active compound (named 4-O-methylhonokiol) from the ethanol extract of Magnolia officinalis. The present study aimed to test two different doses of ethanol extracts of Magnolia officinalis (5 and 10 mg/kg/mouse, p.o., 1 week) and 4-O-methylhonokiol (0.75 and 1.5 mg/kg/mouse, p.o., 1 week) administered for 7 days on memory impairment induced by scopolamine (1 mg/kg body weight i.p.) in mice. Memory and learning were evaluated using the Morris water maze and the step-down avoidance test. Both the ethanol extract of Magnolia officinalis and 4-O-methylhonokiol prevented memory impairment induced by scopolamine in a dose-dependent manner. The ethanol extract of Magnolia officinalis and 4-O-methylhonokiol also dose-dependently attenuated the scopolamine-induced increase of acetylcholinesterase (AChE) activity in the cortex and hippocampus of mice, and inhibited AChE activity in vitro with IC(50) (12 nM). This study, therefore, suggests that the ethanol extract of Magnolia officinalis and its major ingredient, 4-O-methylhonokiol, may be useful for the prevention of the development or progression of AD. Springer Japan 2009-04-04 2009 /pmc/articles/PMC2690856/ /pubmed/19343477 http://dx.doi.org/10.1007/s11418-009-0330-z Text en © The Author(s) 2009 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Original Paper
Lee, Yong Kyung
Yuk, Dong Yeon
Kim, Tae Il
Kim, Young Heui
Kim, Kyoung Tae
Kim, Ki Ho
Lee, Beom Jun
Nam, Sang-Yoon
Hong, Jin Tae
Protective effect of the ethanol extract of Magnolia officinalis and 4-O-methylhonokiol on scopolamine-induced memory impairment and the inhibition of acetylcholinesterase activity
title Protective effect of the ethanol extract of Magnolia officinalis and 4-O-methylhonokiol on scopolamine-induced memory impairment and the inhibition of acetylcholinesterase activity
title_full Protective effect of the ethanol extract of Magnolia officinalis and 4-O-methylhonokiol on scopolamine-induced memory impairment and the inhibition of acetylcholinesterase activity
title_fullStr Protective effect of the ethanol extract of Magnolia officinalis and 4-O-methylhonokiol on scopolamine-induced memory impairment and the inhibition of acetylcholinesterase activity
title_full_unstemmed Protective effect of the ethanol extract of Magnolia officinalis and 4-O-methylhonokiol on scopolamine-induced memory impairment and the inhibition of acetylcholinesterase activity
title_short Protective effect of the ethanol extract of Magnolia officinalis and 4-O-methylhonokiol on scopolamine-induced memory impairment and the inhibition of acetylcholinesterase activity
title_sort protective effect of the ethanol extract of magnolia officinalis and 4-o-methylhonokiol on scopolamine-induced memory impairment and the inhibition of acetylcholinesterase activity
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2690856/
https://www.ncbi.nlm.nih.gov/pubmed/19343477
http://dx.doi.org/10.1007/s11418-009-0330-z
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