The biologically active compound of
Animals
Male
Mice
Anti-Anxiety Agents
/ administration & dosage
Behavior, Animal
/ drug effects
Diazepam
/ pharmacology
Dose-Response Relationship, Drug
Ethanol
/ pharmacology
Flumazenil
/ pharmacology
Maze Learning
/ drug effects
Plant Extracts
/ administration & dosage
Reflex, Righting
/ drug effects
Withania
/ chemistry
Anxiety
GABAA receptors
Withania somnifera
diazepam
docosanyl ferulate
flumazenil
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
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