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Antidepressant Potential of a Functionalized 3-Selanyl Benzo[ b ]Furan Compound in Mice: Focus on the Serotonergic System.

Authors :
Rech TDST
Ribeiro EH
Castro ET
Alves AG
Strelow DN
Neto JSS
Braga AL
BrĂ¼ning CA
Bortolatto CF
Source :
ACS chemical neuroscience [ACS Chem Neurosci] 2023 Mar 15; Vol. 14 (6), pp. 1181-1192. Date of Electronic Publication: 2023 Feb 28.
Publication Year :
2023

Abstract

The present study investigated the antidepressant-like potential of a functionalized 3-selanyl benzo[ b ]furan (SeBZF) in male Swiss mice. To evaluate possible antidepressant-like actions, the compounds SeBZF 1-5 (50 mg/kg, intragastric, i.g., route) were acutely screened in the tail suspension tests (TSTs). The compound 3-((4-methoxyphenyl)selanyl)-2-phenylbenzofuran (SeBZF 3 ) was then selected. Dose-response and time-response curves revealed that SeBFZ 3 exerts antidepressant-like effects in the TST (5-50 mg/kg) and forced swimming test (FST; 50 mg/kg). Additional tests demonstrated that pretreatment with receptor antagonists WAY100635 (5-HT <subscript>1A</subscript> ; 0.1 mg/kg, subcutaneous route), ketanserin (5-HT <subscript>2A/C</subscript> ; 1 mg/kg, intraperitoneal, i.p.), or ondansetron (5-HT <subscript>3</subscript> ; 1 mg/kg, i.p.) blocked the SeBZF 3 antidepressant-like effects (50 mg/kg) in the TST. In addition, the coadministration of subeffective doses of SeBZF 3 (1 mg/kg, i.g.) and fluoxetine (a selective serotonin reuptake inhibitor; 5 mg/kg, i.p.) produced synergistic action. A high dose of SeBZF 3 (300 mg/kg) did not produce oral acute toxicity. The present results provide evidence for the antidepressant-like action of SeBZF 3 and its relative safety, as well as predict the possible interactions with the serotonergic system, aiding in the development of novel options to alleviate psychiatric disabilities.

Details

Language :
English
ISSN :
1948-7193
Volume :
14
Issue :
6
Database :
MEDLINE
Journal :
ACS chemical neuroscience
Publication Type :
Academic Journal
Accession number :
36853167
Full Text :
https://doi.org/10.1021/acschemneuro.2c00816