Evaluation of the antianxiety and antidepressant activities of mosapride in Wistar albino rats.


Journal

Journal of basic and clinical physiology and pharmacology
ISSN: 2191-0286
Titre abrégé: J Basic Clin Physiol Pharmacol
Pays: Germany
ID NLM: 9101750

Informations de publication

Date de publication:
18 Jul 2019
Historique:
received: 24 05 2018
accepted: 15 11 2018
pubmed: 19 7 2019
medline: 7 1 2020
entrez: 19 7 2019
Statut: epublish

Résumé

Background The 5HT4 receptor agonists are antidepressants with a unique mode of action. Many studies have been done on investigational drugs, and mosapride has been shown to have a 5HT3 antagonistic property. In this study, we assessed the potential anxiolytic and antidepressant effects of mosapride on Wistar albino rats. Methods The rats were randomly assigned to two models containing 4 groups of 6 animals each. In the anxiety model, four groups included 0.5 mL of 0.5% carboxymethyl cellulose (CMC), mosapride 1.5 mg/kg, mosapride 3 mg/kg and diazepam 2 mg/kg. They were dosed for 5 days. On the 3rd day, the elevated plus maze (EPM) was conducted, and on the 5th day, the open field (OF) tests were conducted. In the depression model, four groups included 0.5 mL of 0.5% CMC, mosapride 1.5 mg/kg, mosapride 3 mg/kg and imipramine 30 mg/kg. After 3 days of dosing, the forced swim test (FST) was conducted, followed by a washout period of 1 month. Then, the rats were subjected to chronic unpredictable stress with sucrose preference. Results Compared with the control, the mosapride-treated animals showed significant anxiolytic behavior at both high and low doses in the EPM and OF tests. In the FST, both high and low doses of mosapride reduced immobility. The climbing behavior was prominent at a high dose of mosapride, whereas swimming was prominent at a low dose. In the chronic stress model, both doses of mosapride preserved sucrose preference comparable to imipramine. Conclusion These findings suggest that mosapride has anxiolytic and antidepressant activities at clinically used doses.

Identifiants

pubmed: 31318691
doi: 10.1515/jbcpp-2018-0089
pii: jbcpp-2018-0089
doi:

Substances chimiques

Anti-Anxiety Agents 0
Antidepressive Agents 0
Benzamides 0
Morpholines 0
mosapride I8MFJ1C0BY

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Références

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Auteurs

Vybhava Krishna (V)

Kasturba Medical College, Manipal Academy of Higher Education, Pharmacology, MadhavnagarManipal, India.

K L Bairy (KL)

Department of Pharmacology, RAK College of Medical Sciences, RAK Medical and Health Sciences, University, Ras Al Khaimah, UAE.

Navin Patil (N)

Kasturba Medical College, Manipal Academy of Higher Education, Pharmacology, MadhavnagarManipal, India.

Sweenly V Sunny (SV)

Kasturba Medical College, Manipal Academy of Higher Education, Pharmacology, MadhavnagarManipal, India.

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Classifications MeSH