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Protective Effect of Sodium Selenite on 4-Nonylphenol-Induced Hepatotoxicity and Nephrotoxicity in Rats
Murat Boyacioglu1, Ozay Gules2, Hande Sultan Sahiner3
1Department of Pharmacology and Toxicology, Faculty of Veterinary Medicine, Aydın Adnan Menderes University, 09016, Isıklı, Aydın, Turkey. mboyacioglu@adu.edu.tr.
Abstract:
This study was aimed at evaluating the protective effect of sodium selenite (SS) on DNA integrity, antioxidant/oxidant status, and histological changes on 4-nonylphenol (4-NP)-induced toxicity in liver and kidney tissues of rats. Twenty-four adult male Sprague Dawley rats were divided into 4 groups as control, SS, 4-NP, and SS+4-NP group. Control group was untreated. The SS group was supplemented with SS (0.5 mg/kg/day) and the 4-NP group was given 4-NP (125 mg/kg/day). The rats in the SS+4-NP group received SS followed by 4-NP 1 h later at the abovementioned doses. The treatments were administered by oral gavage for 48 days. DNA damage was analyzed by comet assay in lymphocytes. Oxidative stress parameters were measured, and histological evaluation was performed in liver and kidney tissues. Results showed that SS administration significantly decreased % Tail DNA and Mean Tail Moment in SS+4-NP group as compared with 4-NP group. Catalase activity in liver was significantly lower in 4-NP group only. SS treatment significantly increased the glutathione level and decreased high malondialdehyde level in tissues of the SS+4-NP group as compared with 4-NP group. Dilation of central vein, ballooning degeneration, vacuolar degeneration, and deterioration in the structure of remark cords in 4-NP-administered were alleviated in rats that received SS supplementation before administration of 4-NP. Moreover, glycogen intensity in hepatocytes and the wall of central vein increased in the SS+4-NP group. In addition, the SS supplementation in the SS+4-NP group decreased glomerular degeneration as well as the width of cavum glomeruli and congestion intensity in the kidney. These results indicate that SS may have a protective effect against 4-NP-induced hepato-nephrotoxicity in rats.
Insights
Sodium selenite (SS) protects against 4-nonylphenol (4-NP) toxicity by improving DNA integrity and antioxidant status in rat liver and kidney tissues. SS supplementation mitigated 4-NP-induced damage, showing protective effects.
Area of Science:
- Toxicology
- Biochemistry
- Histopathology
Background:
- 4-nonylphenol (4-NP) is an environmental endocrine disruptor with known toxic effects.
- Hepatotoxicity and nephrotoxicity are significant concerns associated with 4-NP exposure.
- Antioxidant strategies are being explored to counteract xenobiotic-induced organ damage.
Purpose of the Study:
- To evaluate the protective role of sodium selenite (SS) against 4-NP-induced toxicity.
- To assess the impact of SS on DNA integrity, oxidative stress markers, and tissue histology in rats exposed to 4-NP.
- To determine if SS can mitigate liver and kidney damage caused by 4-NP.
Main Methods:
- Adult male Sprague Dawley rats were divided into four groups: control, SS, 4-NP, and SS+4-NP.
- Treatments involved oral gavage administration of SS (0.5 mg/kg/day) and 4-NP (125 mg/kg/day) for 48 days.
- Analyses included comet assay for DNA damage, oxidative stress parameter measurements, and histological examination of liver and kidney tissues.
Main Results:
- SS administration significantly reduced DNA damage (% Tail DNA, Mean Tail Moment) in the SS+4-NP group compared to the 4-NP group.
- SS treatment increased glutathione levels and decreased malondialdehyde levels in the SS+4-NP group.
- Histological improvements were observed in the SS+4-NP group, including reduced liver cell degeneration and kidney glomerular damage.
Conclusions:
- Sodium selenite demonstrates a significant protective effect against 4-nonylphenol-induced hepato-nephrotoxicity in rats.
- SS mitigates 4-NP toxicity by preserving DNA integrity, enhancing antioxidant capacity, and improving tissue histology.
- These findings suggest SS as a potential therapeutic agent against 4-NP-induced organ damage.
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