Depression- and anxiogenic-like behaviors induced by lipopolysaccharide in mice are reversed by a selenium-containing indolyl compound: Behavioral, neurochemical and computational insights involving the serotonergic system.
Animals
Anti-Anxiety Agents
/ pharmacology
Antidepressive Agents
/ pharmacology
Anxiety
/ chemically induced
Behavior, Animal
/ drug effects
Depression
/ chemically induced
Disease Models, Animal
Hippocampus
/ drug effects
Indoleamine-Pyrrole 2,3,-Dioxygenase
/ drug effects
Indoles
/ pharmacology
Lipopolysaccharides
Male
Mice
Molecular Docking Simulation
Prefrontal Cortex
/ drug effects
Selenium Compounds
/ pharmacology
Serotonin Plasma Membrane Transport Proteins
/ drug effects
Antidepressant
Anxiolytic
Molecular docking
Neuroinflammation
Organoselenium
Serotonin
Journal
Journal of psychiatric research
ISSN: 1879-1379
Titre abrégé: J Psychiatr Res
Pays: England
ID NLM: 0376331
Informations de publication
Date de publication:
08 2019
08 2019
Historique:
received:
04
02
2019
revised:
09
04
2019
accepted:
02
05
2019
pubmed:
15
5
2019
medline:
21
8
2020
entrez:
15
5
2019
Statut:
ppublish
Résumé
Major depression and anxiety are highly incapacitating psychiatric disorders often present simultaneously, and the causal relationship between these disorders and inflammation are under extensive investigation. The treatment for this comorbidity still relies on drugs acting on the serotonergic neurotransmission, but the modulation of immune-inflammatory pathways has attained an increasing interest in the drug discovery. We have previously demonstrated that the selenoorganic compound 3-[(4-chlorophenyl)selanyl]-1-methyl-1H-indole (CMI) possess antioxidant, anti-inflammatory, antinociceptive and antidepressant-like effect in mice. Considering these pharmacological properties and the structural similarities between tryptophan, serotonin and CMI, the aim of the present study was to investigate whether CMI ameliorates depression- and anxiogenic-like behavior induced by lipopolysaccharide (LPS) in Swiss male mice by modulating the serotonergic system and reducing neuroinflammation. The administration of CMI (1 mg/kg, i.g) reversed the behavioral deficits induced by LPS (0.83 mg/kg, i.p) in the tail suspension test, splash test and elevated plus maze. The pre-treatment of mice with WAY100635 (5-HT
Identifiants
pubmed: 31082651
pii: S0022-3956(19)30151-7
doi: 10.1016/j.jpsychires.2019.05.006
pii:
doi:
Substances chimiques
3-(4-chlorophenylselanyl)-1-methyl-1H-indole
0
Anti-Anxiety Agents
0
Antidepressive Agents
0
Indoleamine-Pyrrole 2,3,-Dioxygenase
0
Indoles
0
Lipopolysaccharides
0
Selenium Compounds
0
Serotonin Plasma Membrane Transport Proteins
0
Slc6a4 protein, mouse
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1-12Informations de copyright
Copyright © 2019. Published by Elsevier Ltd.