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槲寄生提取物和槲皮素可减轻环磷酰胺对小鼠造成的心脏毒性、泌尿毒性和遗传毒性。

Viscum album L. extract and quercetin reduce cyclophosphamide-induced cardiotoxicity, urotoxicity and genotoxicity in mice.

作者信息

Sekeroğlu Vedat, Aydin Birsen, Sekeroğlu Zülal Atli

机构信息

Department of Biology, Faculty of Science, Ordu University, Ordu, Turkey.

出版信息

Asian Pac J Cancer Prev. 2011;12(11):2925-31.

PMID:22393965
Abstract

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 nitrate/nitrite 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.

摘要

评估了槲寄生(VA)甲醇提取物和槲皮素(QE)对环磷酰胺(CP)诱导的小鼠心脏毒性、泌尿毒性和遗传毒性的可能保护作用。单独或与CP联合给予小鼠口服VA(250mg/kg/天)和QE(50mg/kg/天),持续10天。在给予相同剂量的VA和QE 7天后,在实验的第8天和第9天给大鼠腹腔注射CP(40mg/kg)。检测血清、心脏、膀胱和骨髓中的心脏毒性、泌尿毒性和遗传毒性作用。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、还原型谷胱甘肽水平和有丝分裂指数显著降低。当与CP一起给予时,QE完全、VA部分改善了几乎所有检测参数。在用QE和VA联合CP处理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,VA和QE与CP一起预处理显著降低了染色体畸变和畸变细胞。本研究结果表明,补充QE和VA可通过与其降低氧化应激和炎症的能力相关的机制减轻CP诱导的心脏毒性、泌尿毒性和遗传毒性,至少部分是由于其对心血管系统的保护作用。此外,VA和QE可能在癌症化疗期间降低抗肿瘤药物诱导的细胞遗传毒性方面发挥作用。

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