The biologically active compound of


Journal

Journal of psychopharmacology (Oxford, England)
ISSN: 1461-7285
Titre abrégé: J Psychopharmacol
Pays: United States
ID NLM: 8907828

Informations de publication

Date de publication:
Oct 2021
Historique:
pubmed: 4 5 2021
medline: 10 2 2022
entrez: 3 5 2021
Statut: ppublish

Résumé

Clinical and experimental studies support the therapeutic potential of This study was designed to assess whether DF (0.05, 0.25 and 2 mg/kg), similarly to diazepam (2 mg/kg), may exert anxiolytic effects, whether these effects may be significantly blocked by the benzodiazepine antagonist flumazenil (10 mg/kg) and whether DF may lack some of the benzodiazepines' typical motor, cognitive and motivational side effects. The behavioural paradigms Elevated Plus Maze, Static Rods, Novel Object Recognition, Place Conditioning and potentiation of ethanol-induced Loss of Righting Reflex were applied on male CD-1 mice. Similarly to diazepam, DF exerts anxiolytic effects that are blocked by flumazenil. Moreover, at the full anxiolytic dose of 2 mg/kg, DF lacks typical benzodiazepine-like side effects on motor and cognitive performances and on place conditioning. Moreover, DF fails to potentiate ethanol's (3 g/kg) depressant activity at the ethanol-induced Loss of Righting Reflex paradigm. These data point to DF as an effective benzodiazepine-like anxiolytic compound that, in light of its lack of motor, mnemonic and motivational side effects, could be a suitable candidate for the treatment of anxiety disorders.

Sections du résumé

BACKGROUND BACKGROUND
Clinical and experimental studies support the therapeutic potential of
AIMS OBJECTIVE
This study was designed to assess whether DF (0.05, 0.25 and 2 mg/kg), similarly to diazepam (2 mg/kg), may exert anxiolytic effects, whether these effects may be significantly blocked by the benzodiazepine antagonist flumazenil (10 mg/kg) and whether DF may lack some of the benzodiazepines' typical motor, cognitive and motivational side effects.
METHODS METHODS
The behavioural paradigms Elevated Plus Maze, Static Rods, Novel Object Recognition, Place Conditioning and potentiation of ethanol-induced Loss of Righting Reflex were applied on male CD-1 mice.
RESULTS RESULTS
Similarly to diazepam, DF exerts anxiolytic effects that are blocked by flumazenil. Moreover, at the full anxiolytic dose of 2 mg/kg, DF lacks typical benzodiazepine-like side effects on motor and cognitive performances and on place conditioning. Moreover, DF fails to potentiate ethanol's (3 g/kg) depressant activity at the ethanol-induced Loss of Righting Reflex paradigm.
CONCLUSIONS CONCLUSIONS
These data point to DF as an effective benzodiazepine-like anxiolytic compound that, in light of its lack of motor, mnemonic and motivational side effects, could be a suitable candidate for the treatment of anxiety disorders.

Identifiants

pubmed: 33934670
doi: 10.1177/02698811211008588
doi:

Substances chimiques

Anti-Anxiety Agents 0
Diazepam Q3JTX2Q7TU
Ethanol 3K9958V90M
Flumazenil 40P7XK9392
Plant Extracts 0
docosanyl ferulate 0

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1277-1284

Auteurs

Riccardo Maccioni (R)

Department of Life and Environmental Sciences, University of Cagliari, Cagliari, Italy.

Filippo Cottiglia (F)

Department of Life and Environmental Sciences, University of Cagliari, Cagliari, Italy.

Elias Maccioni (E)

Department of Life and Environmental Sciences, University of Cagliari, Cagliari, Italy.

Giuseppe Talani (G)

Institute of Neuroscience, National Research Council (C.N.R.), University Campus, Cagliari, Italy.

Enrico Sanna (E)

Institute of Neuroscience, National Research Council (C.N.R.), University Campus, Cagliari, Italy.
Center of Excellence for the Study of Neurobiology of Addiction, University of Cagliari, Cagliari, Italy.

Valentina Bassareo (V)

Center of Excellence for the Study of Neurobiology of Addiction, University of Cagliari, Cagliari, Italy.
Department of Biomedical Sciences, University of Cagliari, Cagliari, Italy.

Sanjay B Kasture (SB)

Pinnacle Biomedical Research Institute, Bhopal, India.

Elio Acquas (E)

Department of Life and Environmental Sciences, University of Cagliari, Cagliari, Italy.
Center of Excellence for the Study of Neurobiology of Addiction, University of Cagliari, Cagliari, Italy.

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Classifications MeSH