Beneficial role of naringin against methotrexate-induced injury to rat testes: biochemical and ultrastructural analyses

被引:11
作者
Elsawy, Hany [1 ,2 ]
Alzahrani, Abdullah M. [3 ]
Alfwuaires, Manal [3 ]
Abdel-Moneim, Ashraf M. [3 ,4 ]
Khalil, Mahmoud [4 ,5 ]
机构
[1] King Faisal Univ, Coll Sci, Dept Chem, POB 400, Al Hasa 31982, Saudi Arabia
[2] Tanta Univ, Fac Sci, Dept Chem, Tanta, Egypt
[3] King Faisal Univ, Coll Sci, Dept Biol Sci, Al Hasa, Saudi Arabia
[4] Alexandria Univ, Fac Sci, Dept Zool, Alexandria, Egypt
[5] Beirut Arab Univ, Fac Sci, Dept Biol Sci, Beirut, Lebanon
关键词
Methotrexate; naringin; testicular toxicity; oxidative stress; ultrastructure; antioxidants; testosterone; nitric oxide; INDUCED TESTICULAR INJURY; OXIDATIVE STRESS; NITRIC-OXIDE; TOXICITY; PROTECTS; CELLS; DYSFUNCTION; DAMAGE; INFLAMMATION; GRAPEFRUIT;
D O I
10.1080/13510002.2022.2101832
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background Methotrexate (MTX) is a commonly used chemotherapeutic drug that has adverse toxic effects on germ cells. Naringin (NG) is a natural flavanone glycoside, with different phytotherapeutic applications, and its possible protective effects against MTX-induced testicular tissue damage were investigated in this study. Methods Low and high doses of NG (40 and 80 mg/kg/day) were given for 10 days by intraperitoneal (i.p.) injection and MTX (20 mg/kg i.p.) was given at the 4th day of the experiment, with or without NG in rats. Results The obtained results showed that exposure to MTX increased malondialdehyde (MDA) levels and nitric oxide (NO) production compared with the control. In the meantime, MTX depleted catalse (CAT), superoxide dismutase (SOD), glutathione reductase (GR), glutathione peroxidase (GPx), and reduced glutathione (GSH) in the testicular tissue. Further, serum testosterone levels were significantly decreased in the MTX group. NG significantly counteracted the aforementioned effects of MTX; however, NG80 was more effective in restoring SOD, GR, MDA and NO. Interestingly, NG80 achieved a better improvement in the ultrastructural pattern of the testicular cells in MTX-exposed rats. Conclusion These results indicated, for the first time, that NG could be a potential candidate therapy against MTX-reprotoxic impacts.
引用
收藏
页码:158 / 166
页数:9
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