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Protective Effect of Citicoline on Sodium Arsenite-Induced Nephrotoxicity in Mice
被引:0
|作者:
Khodayar, Mohammad Javad
[1
,2
]
Shirani, Maryam
[2
]
Nikravesh, Mehrad
[1
]
Mohammadi, Elaheh
[2
,3
]
Khorsandi, Laya Sadat
[4
]
Shariati, Saeedeh
[1
,2
,3
]
机构:
[1] Ahvaz Jundishapur Univ Med Sci, Fac Pharm, Dept Toxicol, Ahvaz, Iran
[2] Ahvaz Jundishapur Univ Med Sci, Med Basic Sci Res Inst, Toxicol Res Ctr, Ahvaz, Iran
[3] Ahvaz Jundishapur Univ Med Sci, Student Res Comm, Ahvaz, Iran
[4] Ahvaz Jundishapur Univ Med Sci, Med Basic Sci Res Inst, Cellular & Mol Res Ctr, Ahvaz, Iran
关键词:
Sodium Arsenite;
Oxidative Stress;
Inflammation;
Citicoline;
Nephroprotective;
Mice;
DRINKING-WATER;
EXPOSURE;
CANCER;
D O I:
10.5812/jjnpp-144745
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Background: Sodium arsenite (NaAsO2) is a common mineral contaminant in drinking water in numerous parts of the world. It has been shown to have cardiovascular, metabolic, neuroendocrine, and urinary effects on the body. There is abundant scientific evidence that establishes a strong correlation between arsenic exposure and kidney-related disorders. Objectives: The present study aimed to investigate the potential protective effect of citicoline against NaAsO2-induced Methods: The groups included a control group, a group treated with NaAsO2 at a concentration of 50 ppm, a group treated with Cit at a dosage of 1000 mg/kg, and three groups of NaAsO2 (50 ppm) co-treated with Cit at doses of 250, 500, and 1000 mg/kg, Results: Citicoline decreased the level of blood urea nitrogen (P < 0.001), creatinine levels (P < 0.001), thiobarbituric acid reactive substances (P < 0.001), nitric oxide (P < 0.001), inflammatory factors tumor necrosis factor-alpha (P < 0.001) and interleukin-6 (P < 0.001 and P < 0.001). Furthermore, Cit increased total thiol (P < 0.001) and activity levels of catalase (P < 0.05 and P < 0.001), superoxide dismutase (P < 0.01 and P < 0.001), and glutathione peroxidase (P < 0.001). Therefore, Cit reduced the harmful effects caused by the imbalance in oxidative and antioxidant systems and histopathological damage in NaAsO2-intoxicated mice, improving the damage caused by oxidative stress and inflammation. Conclusions: Our research shows that Cit can protect the kidneys against the damaging effects of NaAsO2 by using its antioxidant and anti-inflammatory properties.
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