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Melatonin suppresses cisplatin-induced nephrotoxicity via activation of Nrf-2/HO-1 pathway

机译:褪黑素通过激活Nrf-2 / HO-1途径抑制顺铂诱导的肾毒性

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摘要

BackgroundCisplatin, one of the most effective and potent anticancer drugs, is used in the treatment of a wide variety of both pediatric and adult malignancies. However, the chemotherapeutic use of cisplatin is limited by its serious side-effects such as nephrotoxicity and ototoxicity. Cisplatin chemotherapy induces a reduction in the antioxidant status, leading to a failure of the antioxidant defense against free-radical damage generated by antitumor drugs. Cisplatin-induced oxidative stress in the kidney was partially prevented by antioxidant treatments using superoxide dismutase, glutathione, selenium and flavonoids. Melatonin and its metabolites possess free-radical scavenging activity and it has been shown that they protect against cisplatin toxicity. However, the mechanism of the protective effects of melatonin against cisplatin-induced nephrotoxicity is still essentially unknown. We therefore designed this study to investigate the underlying mechanism of the protective effect of melatonin against cisplatin-induced renal damage in a rat nephrotoxicity model in vivo.
机译:背景顺铂是最有效,最有效的抗癌药物之一,可用于治疗各种儿科和成人恶性肿瘤。但是,顺铂的化学治疗方法受到其严重的副作用(如肾毒性和耳毒性)的限制。顺铂化疗导致抗氧化剂状态降低,导致抗氧化剂防御抗肿瘤药物产生的自由基损伤的能力下降。使用超氧化物歧化酶,谷胱甘肽,硒和类黄酮的抗氧化剂治疗可部分预防顺铂引起的肾脏氧化应激。褪黑素及其代谢产物具有自由基清除活性,并且已经表明它们可以抵抗顺铂毒性。但是,褪黑素对顺铂诱导的肾毒性的保护作用机理仍然是未知的。因此,我们设计了这项研究,以研究褪黑激素在体内大鼠肾毒性模型中对顺铂诱导的肾损害的保护作用的潜在机制。

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