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Evaluation of the antioxidative potential of diisopropyldithiocarbamates sodium salt on diclofenac-induced toxicity in male albino rats.

Authors :
Tella T
Adegbegi A
Emeninwa C
Odola A
Ayangbenro A
Adaramoye O
Source :
Toxicology reports [Toxicol Rep] 2022 Apr 09; Vol. 9, pp. 828-833. Date of Electronic Publication: 2022 Apr 09 (Print Publication: 2022).
Publication Year :
2022

Abstract

Diclofenac (DIC) is a non-steroidal anti-inflammatory drug (NSAID) which is known to induce oxidative stress. Dithiocarbamates are compounds with proven antioxidant effect. The aim of the present study was to investigate the antioxidant capacity of diisopropyldithiocarbamates sodium salt (a synthetized compound) (Na(i-Pr <subscript>2</subscript> dtc) ) against diclofenac-induced toxicity in the testes of male Wistar albino rats. The animals were assigned into six groups of six rats each. Group 1 (control) received corn oil, Groups 2, 3, 4, 5, 6 received DIC (100 mg/kg), DIC and (Na(i-Pr <subscript>2</subscript> dtc) (30 mg/kg), DIC and vitamin E (30 mg/kg), (Na(i-Pr <subscript>2</subscript> dtc) (30 mg/kg) and vitamin E only respectively. Our findings show that treatment with DIC significantly reduced superoxide dismutase (SOD) activity by 42% compared to normal control (NC) animals. In DIC treated group, Na(i-Pr <subscript>2</subscript> dtc) caused a 17% elevation of catalase (CAT) activity compared to DIC only group. Reduced glutathione level was significantly reduced in DIC only treated group when compared with DIC and VIT E treated group. Photomicrographs of testis from Na(i-Pr <subscript>2</subscript> dtc) treated rats showed normal seminiferous epithelium with no lesions. In conclusion, Na(i-Pr <subscript>2</subscript> dtc) has antioxidant properties.<br />Competing Interests: The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (© 2022 The Authors.)

Details

Language :
English
ISSN :
2214-7500
Volume :
9
Database :
MEDLINE
Journal :
Toxicology reports
Publication Type :
Academic Journal
Accession number :
36518424
Full Text :
https://doi.org/10.1016/j.toxrep.2022.03.052