Worsening of the Toxic Effects of (±)Cis-4,4'-DMAR Following Its Co-Administration with (±)Trans-4,4'-DMAR: Neuro-Behavioural, Physiological, Immunohistochemical and Metabolic Studies in Mice.

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License: CC BY 4.0
Serval ID
serval:BIB_4D92C3CAF74D
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Worsening of the Toxic Effects of (±)Cis-4,4'-DMAR Following Its Co-Administration with (±)Trans-4,4'-DMAR: Neuro-Behavioural, Physiological, Immunohistochemical and Metabolic Studies in Mice.
Journal
International journal of molecular sciences
Author(s)
Tirri M., Frisoni P., Bilel S., Arfè R., Trapella C., Fantinati A., Corli G., Marchetti B., De-Giorgio F., Camuto C., Mazzarino M., Gaudio R.M., Serpelloni G., Schifano F., Botrè F., Marti M.
ISSN
1422-0067 (Electronic)
ISSN-L
1422-0067
Publication state
Published
Issued date
16/08/2021
Peer-reviewed
Oui
Volume
22
Number
16
Language
english
Notes
Publication types: Journal Article
Publication Status: epublish
Abstract
4,4'-Dimethylaminorex (4,4'-DMAR) is a new synthetic stimulant, and only a little information has been made available so far regarding its pharmaco-toxicological effects. The aim of this study was to investigate the effects of the systemic administration of both the single (±)cis (0.1-60 mg/kg) and (±)trans (30 and 60 mg/kg) stereoisomers and their co-administration (e.g., (±)cis at 1, 10 or 60 mg/kg + (±)trans at 30 mg/kg) in mice. Moreover, we investigated the effect of 4,4'-DMAR on the expression of markers of oxidative/nitrosative stress (8-OHdG, iNOS, NT and NOX2), apoptosis (Smac/DIABLO and NF-κB), and heat shock proteins (HSP27, HSP70, HSP90) in the cerebral cortex. Our study demonstrated that the (±)cis stereoisomer dose-dependently induced psychomotor agitation, sweating, salivation, hyperthermia, stimulated aggression, convulsions and death. Conversely, the (±)trans stereoisomer was ineffective whilst the stereoisomers' co-administration resulted in a worsening of the toxic (±)cis stereoisomer effects. This trend of responses was confirmed by immunohistochemical analysis on the cortex. Finally, we investigated the potentially toxic effects of stereoisomer co-administration by studying urinary excretion. The excretion study showed that the (±)trans stereoisomer reduced the metabolism of the (±)cis form and increased its amount in the urine, possibly reflecting its increased plasma levels and, therefore, the worsening of its toxicity.
Keywords
Animals, Behavior, Animal/drug effects, Male, Mice, Mice, Inbred ICR, Oxazoles/classification, Oxazoles/toxicity, Oxazoles/urine, Psychophysiologic Disorders/chemically induced, Psychophysiologic Disorders/metabolism, Psychophysiologic Disorders/pathology, Psychotropic Drugs/classification, Psychotropic Drugs/toxicity, Psychotropic Drugs/urine, Stereoisomerism, 4-4′-DMAR, apoptosis, cortex, drug metabolism, hyperthermia, immunohistochemistry, neurotoxicity, novel psychoactive substances, oxidative/nitrosative stress, stimulant
Pubmed
Web of science
Open Access
Yes
Create date
21/09/2021 14:30
Last modification date
23/01/2024 8:25
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