A honokiol-enriched Magnolia officinalis Rehder & E.H. Wilson. bark extract possesses anxiolytic-like activity with neuroprotective effect through the modulation of CB1 receptor.
Animals
Anti-Anxiety Agents
/ pharmacology
Anxiety
/ drug therapy
Anxiety Disorders
/ drug therapy
Behavior, Animal
/ drug effects
Biphenyl Compounds
/ pharmacology
Brain
Brain-Derived Neurotrophic Factor
/ metabolism
GABA Modulators
/ pharmacology
Humans
Lignans
/ pharmacology
Magnolia
/ chemistry
Male
Mice
Neuroprotective Agents
/ pharmacology
Phytotherapy
Plant Bark
/ chemistry
Plant Extracts
/ pharmacology
Receptor, Cannabinoid, CB1
/ agonists
Magnolia officinalis
CB1
Honokiol
anxiety
neuroprotection
Journal
The Journal of pharmacy and pharmacology
ISSN: 2042-7158
Titre abrégé: J Pharm Pharmacol
Pays: England
ID NLM: 0376363
Informations de publication
Date de publication:
12 Aug 2021
12 Aug 2021
Historique:
received:
19
01
2021
accepted:
12
04
2021
pubmed:
6
5
2021
medline:
11
1
2022
entrez:
5
5
2021
Statut:
ppublish
Résumé
The exposure of neurons to an excessive excitatory stimulation induces the alteration of the normal neuronal function. Mood disorders are among the first signs of alterations in the central nervous system function. Magnolia officinalis bark extract has been extensively used in the traditional medicine systems of several countries, showing several pharmacological activities. Honokiol, the main constituent of M. officinalis, is a GABA modulator and a CB1 agonist, which is deeply investigated for its role in modulating mood disorders. Thus, we evaluated the possible neuroprotective effect of a standardized M. officinalis bark extract (MOE), enriched in honokiol, and its effect on animal mood behavioural tests and in an in vitro model of excitotoxicity. MOE showed neuroprotective effect using SH-SY5Y cells, by normalizing brain-derived neurotrophic factor release. Then, we tested the effect of MOE in different behavioural tests evaluating anxiety and depression and we observed a selective anxiolytic-like effect. Finally, we confirmed the involvement of CB1 in the final effect of MOE by the co-administration of the CB1 antagonist, AM251. These results suggest that MOE could be considered an effective and safe anxiolytic candidate with neuroprotective activity.
Identifiants
pubmed: 33950239
pii: 6265594
doi: 10.1093/jpp/rgab067
doi:
Substances chimiques
Anti-Anxiety Agents
0
Bdnf protein, mouse
0
Biphenyl Compounds
0
Brain-Derived Neurotrophic Factor
0
GABA Modulators
0
Lignans
0
Neuroprotective Agents
0
Plant Extracts
0
Receptor, Cannabinoid, CB1
0
honokiol
11513CCO0N
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
1161-1168Informations de copyright
© The Author(s) 2021. Published by Oxford University Press on behalf of the Royal Pharmaceutical Society. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.