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10.5487/TR.2018.34.2.133

http://scihub22266oqcxt.onion/10.5487/TR.2018.34.2.133
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C5903139!5903139!29686775
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suck abstract from ncbi


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pmid29686775      Toxicol+Res 2018 ; 34 (2): 133-41
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  • Beneficial Effects of Cynaroside on Cisplatin-Induced Kidney Injury In Vitro and In Vivo #MMPMID29686775
  • Nho JH; Jung HK; Lee MJ; Jang JH; Sim MO; Jeong DE; Cho HW; Kim JC
  • Toxicol Res 2018[Apr]; 34 (2): 133-41 PMID29686775show ga
  • Anti-cancer drugs such as cisplatin and doxorubicin are effectively used more than radiotherapy. Cisplatin is a chemotherapeutic drug, used for treatment of various forms of cancer. However, it has side effects such as ototoxicity and nephrotoxicity. Cisplatin-induced nephrotoxicity increases tubular damage and renal dysfunction. Consequently, we investigated the beneficial effect of cynaroside on cisplatin-induced kidney injury using HK-2 cell (human proximal tubule cell line) and an animal model. Results indicated that 10 ?M cynaroside diminished cisplatin-induced apoptosis, mitochondrial dysfunction and caspase-3 activation, cisplatin-induced upregulation of caspase-3/MST-1 pathway decreased by treatment of cynaroside in HK-2 cells. To confirm the effect of cynaroside on cisplatin-induced kidney injury in vivo, we used cisplatin exposure animal model (20 mg/kg, balb/c mice, i.p., once a day for 3 days). Renal dysfunction, tubular damage and neutrophilia induced by cisplatin injection were decreased by cynaroside (10 mg/kg, i.p., once a day for 3 days). Results indicated that cynaroside decreased cisplatin-induced kidney injury in vitro and in vivo, and it could be used for improving cisplatin-induced side effects. However, further experiments are required regarding toxicity by high dose cynaroside and caspase-3/MST-1-linked signal transduction in the animal model.
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