The protective effects of hesperidin and curcumin on 5-fluorouracil-induced nephrotoxicity in mice

被引:43
作者
Gelen, Volkan [1 ]
Sengul, Emin [2 ]
Yildirim, Serkan [3 ]
Senturk, Esra [4 ]
Tekin, Samet [2 ]
Kukurt, Abdulsamed [5 ]
机构
[1] Kafkas Univ, Vet Fac, Dept Physiol, Kars, Turkey
[2] Ataturk Univ, Vet Fac, Dept Physiol, Erzurum, Turkey
[3] Ataturk Univ, Vet Fac, Dept Pathol, Erzurum, Turkey
[4] Ibrahim Cecen Univ Agri, Sch Hlth Serv, Agri, Turkey
[5] Kafkas Univ, Vet Fac, Dept Biochem, Kars, Turkey
关键词
Nephrotoxicity; Apoptosis; Curcumin; Hesperidin; Histopathology; Immunohistochemistry; Mice; OXIDATIVE STRESS; INDUCED TOXICITY; DAMAGE; QUERCETIN; INFLAMMATION; RATS; HEPATOTOXICITY; CHEMOTHERAPY; ANTIOXIDANT; INHIBITION;
D O I
10.1007/s11356-021-13969-5
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Nephrotoxicity is a very important complication of 5-fluorouracil (5-FU)-treated cancer patients. Increased oxidative stress, kidney damage, and apoptosis play an important role in the pathogenesis of nephrotoxicity caused by 5-FU. In this study, protective effects of two natural compounds, hesperidin and curcumin, on experimentally induced kidney damage in mice with 5-FU were determined. Application of 5-FU resulted in severe histopathological changes and severe renal failure with increased serum urea and creatinine levels. Also, 5-FU-induced kidney damage, increased levels of malondialdehyde (MDA), decreased superoxide dismutase (SOD), catalase (CAT), glutathione reductase (GR) activity, and glutathione (GSH) level have been demonstrated. Also, where 5-FU is in the concentration of caspase-3 and 8-OHdG immune-positive cells and therefore causes apoptosis and DNA damage in kidney tissue cells. However, especially high doses of hesperidin and curcumin treatment significantly improved 5-FU-induced oxidative stress/lipid peroxidation, apoptosis/DNA damage, and renal dysfunction. Based on these data, our results suggest that hesperidin and curcumin may be used as new and promising agents against 5-FU-induced nephrotoxicity.
引用
收藏
页码:47046 / 47055
页数:10
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