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Viscum album L. Extract and Quercetin Reduce Cyclophosphamide-Induced Cardiotoxicity, Urotoxicity and Genotoxicity in Mice

机译:Viscum album L.提取物和槲皮素可降低环磷酰胺诱导的小鼠心脏毒性,尿毒性和基因毒性

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Possible protective effects of a methanolic extract of Viscum album (VA) and quercetin (QE) against cyclophosphamide (CP) induced cardiotoxicity, urotoxicity and genotoxicity in mice were evaluated. Mice were administered orally VA (250 mg/kg/day) and QE (50 mg/kg/day) for 10 days alone or in combination with CP. After the same doses of VA and QE given for 7 days, rats were intraperitoneally administered CP (40 mg/kg) on days 8 and 9 of the experiment. Cardiotoxic, urotoxic and genotoxic effects were examined in serum, heart, bladder and bone marrow. Significant decreases in the levels of antioxidant enzymes (superoxide dismutase, catalase and glutathione peroxidase), glutathione-S-transferases, reduced glutathione and mitotic index were observed. QE completely and VA partly ameliorated almost of all the examined parameters when given together with CP. Higher total nitrateitrite levels were observed in the myocardial tissue treated with QE and VA in combination with CP. In addition, the pre-treatment with VA and QE together with CP significantly decreased chromosome aberrations and aberrant cells compared to CP alone. Results from the current study suggest that QE and VA supplementation attenuates CP induced cardiotoxicity, urotoxicity and genotoxicity through a mechanism related to their ability to decrease oxidative stress and inflammation, and at least in part to its protective effects on the cardiovascular system. In addition, VA and QE may play a role in reducing cytogenotoxicity induced by anti-neoplastic drugs during cancer chemotherapy.
机译:评估了Viscum Album(VA)和槲皮素(QE)的甲醇提取物对环磷酰胺(CP)诱导的小鼠心脏毒性,尿毒症和遗传毒性的保护作用。单独或与CP联合口服VA(250 mg / kg /天)和QE(50 mg / kg /天)连续10天。在连续7天给予相同剂量的VA和QE后,在实验的第8天和第9天对大鼠腹膜内给予CP(40 mg / kg)。在血清,心脏,膀胱和骨髓中检查了心脏毒性,尿毒性和遗传毒性。观察到抗氧化酶(超氧化物歧化酶,过氧化氢酶和谷胱甘肽过氧化物酶),谷胱甘肽-S-转移酶,谷胱甘肽和有丝分裂指数降低的水平显着下降。与CP一起使用时,QE完全改善了,VA几乎部分改善了所有检查的参数。在QE和VA结合CP治疗的心肌组织中观察到较高的总硝酸盐/亚硝酸盐水平。此外,与单独使用CP相比,使用VA和QE以及CP进行预处理可以显着降低染色体畸变和异常细胞。当前研究的结果表明,补充QE和VA可以通过一种与CP减少氧化应激和炎症的能力有关的机制来减弱CP引起的心脏毒性,尿毒性和遗传毒性,并且至少部分与其对心血管系统的保护作用有关。另外,VA和QE可能在减少癌症化疗期间抗肿瘤药物诱导的细胞遗传毒性中起作用。

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