Chemoprotective effects of curcumin on doxorubicin-induced nephrotoxicity in wistar rats: by modulating inflammatory cytokines, apoptosis, oxidative stress and oxidative DNA damage

被引:101
作者
Benzer, Fulya [1 ]
Kandemir, Fatih Mehmet [2 ]
Kucukler, Sefa [2 ]
Comakli, Selim [3 ]
Caglayan, Cuneyt [4 ]
机构
[1] Munzur Univ, Fac Engn, Dept Food Engn, Tunceli, Turkey
[2] Ataturk Univ, Fac Vet Med, Dept Biochem, Erzurum, Turkey
[3] Ataturk Univ, Fac Vet Med, Dept Pathol, Erzurum, Turkey
[4] Bingol Univ, Fac Vet Med, Dept Biochem, Bingol, Turkey
关键词
Apoptosis; curcumin; doxorubicin; inflammation; nephrotoxicity; IN-VIVO; INDUCED CARDIOTOXICITY; INDUCED TOXICITY; KAPPA-B; ANTIOXIDANT; MITOCHONDRIAL; PEROXIDASE; RESISTANCE; CHRYSIN; AKT;
D O I
10.1080/13813455.2017.1422766
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
Doxorubicin (DXR) is one of the most important chemotherapeutic agent. However, nephrotoxicity reduces its clinical utility in humans. The aim of the study was to investigate protective effects of curcumin (CMN) against DXR-induced nephrotoxicity. Rats were subjected to oral treatment of CMN (100 and 200 mg/kg body weight) for 7 days. Nephrotoxicity was induced by single intra peritoneal injection of DXR (40 mg/kg body weight) on the fifth day and then the experiment was terminated on the eighth day. Nephroprotective effects of CMN were associated with decrease in serum toxicity markers and increase in antioxidant enzyme activities. CMN was able to reduced the levels of inflammatory markers such as TNF-alpha, NF-kappa B, IL-1 beta, iNOS and COX-2 in the rats. It also reduced the expressions of apoptotic marker including caspase-3, and oxidative DNA damage marker including 8-OHdG. Collectively, these findings indicated that CMN protect against DXR-induced nephrotoxicity.
引用
收藏
页码:448 / 457
页数:10
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