首页> 外文期刊>Protoplasma: An International Journal of Cell Biology >Neuroprotective activities of curcumin and quercetin with potential relevance to mitochondrial dysfunction induced by oxaliplatin
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Neuroprotective activities of curcumin and quercetin with potential relevance to mitochondrial dysfunction induced by oxaliplatin

机译:姜黄素和槲皮素的神经保护活性可能与奥沙利铂诱导的线粒体功能障碍有关

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Peripheral neurotoxicity is one of the serious dose-limiting side effects of oxaliplatin (Oxa) when used in the treatment of malignant conditions. It is documented that it elicits major side effects specifically neurotoxicity due to oxidative stress forcing the patients to limit its clinical use in long-term treatment. Oxidative stress has been proven to be involved in Oxa-induced toxicity including neurotoxicity. The mitochondria have recently emerged as targets for anticancer drugs in various kinds of toxicity including neurotoxicity that can lead to neoplastic disease. However, there is paucity of literature involving the role of the mitochondria in mediating Oxa-induced neurotoxicity and its underlying mechanism is still debatable. The purpose of this study was to investigate the dose-dependent damage caused by Oxa on isolated brain mitochondria under in vitro conditions. The study was also designed to investigate the neuroprotective effects of nutraceuticals, curcumin (CMN), and quercetin (QR) on Oxa-induced mitochondrial oxidative stress and respiratory chain complexes in the brain of rats. Oxidative stress biomarkers, levels of nonenzymatic antioxidants, activities of enzymatic antioxidants, and mitochondrial complexes were evaluated against the neurotoxicity induced by Oxa. Pretreatment with CMN and QR significantly replenished the mitochondrial lipid peroxidation levels and protein carbonyl content induced by Oxa. CMN and QR ameliorated altered nonenzymatic and enzymatic antioxidants and complex enzymes of mitochondria. We conclude that CMN and QR, by attenuating oxidative stress as evident by mitochondrial dysfunction, hold promise as agents that can potentially reduce Oxa-induced adverse effects in the brain.
机译:当用于治疗恶性疾病时,周围神经毒性是奥沙利铂(Oxa)的严重剂量限制副作用之一。据记录,由于氧化应激,它引起主要副作用,特别是神经毒性,迫使患者限制其在长期治疗中的临床应用。氧化应激已被证明与Oxa诱导的毒性有关,包括神经毒性。线粒体已成为抗癌药物的靶标,具有多种毒性,包括可导致肿瘤性疾病的神经毒性。但是,很少有文献报道线粒体在介导Oxa诱导的神经毒性中的作用,其潜在机制尚有争议。这项研究的目的是在体外条件下研究Oxa对孤立的脑线粒体造成的剂量依赖性损伤。该研究还旨在研究营养保健品,姜黄素(CMN)和槲皮素(QR)对Oxa诱导的大鼠脑线粒体氧化应激和呼吸链复合物的神经保护作用。评估了氧化应激生物标志物,非酶抗氧化剂的水平,酶抗氧化剂的活性和线粒体复合物对Oxa诱导的神经毒性。用CMN和QR预处理可显着补充Oxa诱导的线粒体脂质过氧化水平和蛋白质羰基含量。 CMN和QR改善了线粒体的非酶和酶抗氧化剂和复合酶的变化。我们得出的结论是,CMN和QR通过减轻线粒体功能障碍所表现出的氧化应激,有望作为可能减少Oxa诱导的脑部不良反应的药物。

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