Oxidative stress profile following the co-administration of cisplatin and resveratrol in female rats: a preliminary study
Author(s) -
Izuchukwu Azuka Okafor
Publication year - 2021
Publication title -
physiology and pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.2
H-Index - 11
eISSN - 2476-5244
pISSN - 2476-5236
DOI - 10.32598/ppj.25.2.90
Subject(s) - malondialdehyde , oxidative stress , superoxide dismutase , intraperitoneal injection , lipid peroxidation , glutathione , medicine , catalase , pharmacology , endocrinology , kidney , glutathione reductase , chemistry , glutathione peroxidase , biochemistry , enzyme
Cisplatin is one of the most widely used drugs for the treatment of various cancers but has oxidative tissue damage as one of its side effects. This study investigated the oxidative stress profile in some important body tissues following the co-administration of cisplatin (CIS) and resveratrol (RSV). Methods: Thirty-five adult female rats with an average body weight of 162g were divided into 5 groups (n=7) and used for this experimental study. Group A served as the normal control group and received distilled water only. Group B received only a single dose intraperitoneal injection of 10mg/kg CIS. Groups C, D and E were orally given 5, 10 and 20mg/kg of RSV respectively for 7 days, starting 24h after a single CIS dose intraperitoneal injection of 10mg/kg. Selected body tissues were harvested for oxidative stress profiling at the end of the experiment. Results: CIS significantly increased malondialdehyde levels and decreased glutathione, superoxide dismutase and catalase levels in all the tissues assessed (ovary, uterus, liver, kidney, pancreas, stomach and spleen) when compared to the normal control. The RSV treatment caused the reversal of these effects; malondialdehyde levels were significantly decreased, while glutathione, superoxide dismutase and catalase levels were significantly increased across all the examined tissues. Conclusion: RSV at different doses could be effective in the management of CIS-induced oxidative stress and lipid peroxidation across some body tissues. However, this effect may be dependent on the dose of CIS and RSV.
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