3-(4-Chlorophenylselanyl)-1-methyl-1H-indole promotes recovery of neuropathic pain and depressive-like behavior induced by partial constriction of the sciatic nerve in mice.
Animals
Anti-Inflammatory Agents
/ therapeutic use
Antidepressive Agents
/ therapeutic use
Antioxidants
/ therapeutic use
Corticosterone
Hippocampus
/ drug effects
Indoles
/ therapeutic use
Lipid Peroxidation
/ drug effects
Male
Mice
Neuralgia
/ blood
Reactive Oxygen Species
/ blood
Sciatic Nerve
/ drug effects
Selenium
/ blood
Selenium Compounds
/ therapeutic use
Swimming
/ physiology
Comorbidity
Depression
Indole
Pain
Selenium
Journal
Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements (GMS)
ISSN: 1878-3252
Titre abrégé: J Trace Elem Med Biol
Pays: Germany
ID NLM: 9508274
Informations de publication
Date de publication:
Jul 2019
Jul 2019
Historique:
received:
28
11
2018
revised:
18
04
2019
accepted:
23
04
2019
entrez:
22
5
2019
pubmed:
22
5
2019
medline:
22
11
2019
Statut:
ppublish
Résumé
3-(4-Chlorophenylselanyl)-1-methyl-1H-indole (CMI) is an organoselenium compound that presents antioxidant activity, antinociceptive, anti-inflammatory and antidepressive-like effect in mice in previous studies conducted by our research group. In this study, we evaluate the anti-allodynic, anti-hyperalgesic and antidepressant-like effects of CMI on partial sciatic nerve ligation (PSNL) in male adult Swiss mice (25-35 g) as well as the involvement of oxidative stress in these effects. Mice underwent PSNL surgery and after 4 weeks they were treated with CMI (10 mg/kg, intragastric route [i.g.]) or vehicle. The treatment with CMI (10 mg/kg, i.g.) reversed the increased the percentage of response to Von-Frey Hair (VFH) stimulation, decreased the latency time to nociceptive response in the hot-plate test, increased immobility time in the forced swimming test (FST) and decreased groomings activity in the splash test, all induced by PSNL. Additionally, CMI also reversed increased the levels of reactive oxygen species (ROS) and lipid peroxidation in cortex and hippocampus and plasmatic levels of corticosterone in mice, induced by PSNL. Results demonstrate that CMI reversed behavioral and biochemical alterations in the dyad pain-depression induced by PSNL and possibly modulation of oxidative system.
Identifiants
pubmed: 31109602
pii: S0946-672X(18)30743-0
doi: 10.1016/j.jtemb.2019.04.014
pii:
doi:
Substances chimiques
3-(4-chlorophenylselanyl)-1-methyl-1H-indole
0
Anti-Inflammatory Agents
0
Antidepressive Agents
0
Antioxidants
0
Indoles
0
Reactive Oxygen Species
0
Selenium Compounds
0
Selenium
H6241UJ22B
Corticosterone
W980KJ009P
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
126-133Informations de copyright
Copyright © 2019. Published by Elsevier GmbH.