荨麻通过抑制组织损伤、氧化应激和脂质过氧化作用对抗阿霉素诱导的大鼠心脏毒性

M. Erboğa, Yeliz Bozdemir Donmez, U. Sener, Z. Erboğa, C. Aktas, M. Kanter
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引用次数: 8

摘要

目的:阿霉素(DOX)是一种高效的抗癌药物,因其严重的心脏毒性而限制了临床应用。杜鹃花种子具有较强的抗氧化作用,在民间医学中被广泛应用,特别是在晚期癌症患者的治疗中。本研究的目的是探讨UD对dox诱导的心脏毒性的保护作用。方法:UD治疗组大鼠腹腔注射2 ml/kg UD。为了诱导心脏毒性,采用单剂量腹腔注射DOX 30 mg/kg, 48 h后处死大鼠。结果:本研究首次揭示了UD对doxin诱导的心脏毒性的保护作用。UD治疗对doxin引起的心肌损伤有明显的保护作用,心肌损伤以传导异常、空泡化、炎症细胞浸润、出血和肌纤维紊乱为特征。DOX作为氧化应激的指标,引起脂质过氧化反应显著增加,抗氧化酶活性降低;超氧化物歧化酶,谷胱甘肽过氧化物酶和过氧化氢酶。UD处理可显著减轻doxin诱导的氧化损伤。结论:UD可能是一种较好的抗DOX毒性的心脏保护剂。
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Effect of Urtica Dioica against Doxorubicin-InducedCardiotoxicity in Rats through Suppression ofHistological Damage, Oxidative Stress and LipidPeroxidation
Objective: Doxorubicin (DOX) is a highly effective anti-cancer drug with limited clinical use due to its serious cardiotoxicity. Urtica dioica L. seeds (UD), have been widely used in folk medicine, particularly in the therapy for advanced cancer patients, possesses a potent anti-oxidant properties. The goal of present study was to investigate the cardioprotective effects of UD on DOX-induced cardiotoxicity. Method: The rats in the UD treated group were given intraperitoneally 2 ml/kg UD. To induce cardiotoxicity, 30 mg/kg DOX was injected intraperitoneally by a single dose and the rats were sacrificed after 48 h. Results: The present study revealed for the first time a protective role of UD against DOXinduced cardiotoxicity. UD therapy significantly protected against DOXinduced myocardial damage which was characterized by conduction abnormalities, vacuolization, inflammatory cell infiltration, hemorrhag es, and myofibrillar disarrangement. As indicators of oxidative stress, DOX caused significantly increase lipid peroxidation and reduction in activities of antioxidant enzymes; superoxide dismutase, glutathione peroxidase, and catalase. UD treatment significantly attenuated DOXinduced oxidative injury. Conclusion: The present study showed that UD might be a suitable cardioprotector against toxic effects of DOX.
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