A honokiol-enriched Magnolia officinalis Rehder & E.H. Wilson. bark extract possesses anxiolytic-like activity with neuroprotective effect through the modulation of CB1 receptor.


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
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

1161-1168

Informations 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.

Auteurs

Vittoria Borgonetti (V)

Department of Neuroscience, Psychology, Drug Research and Child Health (NEUROFARBA), Section of Pharmacology, University of Florence, Florence, Italy.

Paolo Governa (P)

Department of Biotechnology, Chemistry and Pharmacy - Department of Excellence 2018-2022, University of Siena Siena, Italy.

Fabrizio Manetti (F)

Department of Biotechnology, Chemistry and Pharmacy - Department of Excellence 2018-2022, University of Siena Siena, Italy.

Elisabetta Miraldi (E)

Department of Physical Sciences, Earth and Environment, University of Siena, Siena, Italy.

Marco Biagi (M)

Department of Physical Sciences, Earth and Environment, University of Siena, Siena, Italy.

Nicoletta Galeotti (N)

Department of Neuroscience, Psychology, Drug Research and Child Health (NEUROFARBA), Section of Pharmacology, University of Florence, Florence, Italy.

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Classifications MeSH