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Protective but Non-Synergistic Effects of Nigella Sativa and Vitamin E against Cisplatin-Induced Renal Toxicity and Oxidative Stress in Wistar Rats.
- Source :
-
Drug research [Drug Res (Stuttg)] 2018 Dec; Vol. 68 (12), pp. 696-703. Date of Electronic Publication: 2018 Jun 26. - Publication Year :
- 2018
-
Abstract
- Background: Cisplatin is an anti-cancer drug that causes nephrotoxicity and oxidative stress. Extracts of Nigella sativa is nephroprotective. Vitamin E is also a potent antioxidant. This study sought to determine a possible synergistic effect of administering the two agents prior to cisplatin use on nephrotoxicity and oxidative stress.<br />Methods: 48 male Wistar rats were randomly divided into 6 groups of 8 rats each. Group I served as the control. Group II received cisplatin without any treatment for 6 days. Groups III, IV, V and VI received 100 mg/kg Nigella sativa (NS), 200 mg/kg NS, 100 mg/kg Vitamin E and 200 mg/kg NS+100 mg/kg Vitamin E respectively for 5 days prior to 6 days administration of cisplatin. On the last day of the experiment, all the animals were sacrificed and serum samples collected for analysis.<br />Results: Cisplatin administration caused a significant increase in creatinine level (p<0.01), urea level (p<0.01), sodium concentration and malondialdehyde level (p<0.001). Pre-administration with NS caused a significant reduction in creatinine level (p<0.001), urea level (p<0.001), sodium concentration (p<0.001) and malondialdehyde (p<0.01) level. Pre-administration with vitamin E caused a significant reduction in creatinine level (p<0.001), urea level (p<0.01), sodium concentration (p<0.001) and malondialdehyde level. They both also caused a significant increase in superoxide dismutase, reduced glutathione and catalase (CAT) levels. The combination of NS and vitamin E however did not show significant synergistic effects.<br />Conclusion: These results suggest that even though pre-administration of the two agents protect against renal toxicity and oxidative stress, the effects are however not collaborative.<br />Competing Interests: The authors declare that there was no conflict of interests.<br /> (© Georg Thieme Verlag KG Stuttgart · New York.)
- Subjects :
- Animals
Catalase blood
Creatinine blood
Disease Models, Animal
Humans
Kidney drug effects
Kidney metabolism
Kidney Diseases blood
Kidney Diseases chemically induced
Male
Malondialdehyde blood
Oxidative Stress drug effects
Plant Extracts therapeutic use
Protective Agents therapeutic use
Random Allocation
Rats
Rats, Wistar
Superoxide Dismutase blood
Urea blood
Cisplatin adverse effects
Kidney Diseases prevention & control
Nigella sativa chemistry
Plant Extracts pharmacology
Protective Agents pharmacology
Vitamin E administration & dosage
Subjects
Details
- Language :
- English
- ISSN :
- 2194-9387
- Volume :
- 68
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- Drug research
- Publication Type :
- Academic Journal
- Accession number :
- 29945276
- Full Text :
- https://doi.org/10.1055/a-0626-7003