生姜提取物对环磷酰胺致成年雄性白化大鼠心脏毒性的保护作用

N. Shalaby, A. Mahmoud, Nagah El-Sayed M. Ali, Nahla E. Ibrahem, Noura H. Mekawy
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引用次数: 3

摘要

环磷酰胺是一种细胞毒性烷基化剂,是一种广泛使用的抗肿瘤药物。心脏毒性被认为是其使用的限制性副作用之一,这归因于氧化应激。生姜是抗自由基和氧化攻击的强力抗氧化剂。本研究旨在探讨officinale对环磷酰胺诱导的成年雄性白化大鼠心脏毒性的保护作用。选用成年雄性白化大鼠30只,分为5组;Ia组(-ve对照组)、Ib组(+ve对照组)、II组(铁皮水芹治疗组);200 mg/kg/天口服),III组(环磷酰胺处理组;单剂量150 mg/kg I.P.)和IV组(环磷酰胺和officinale处理组;大鼠照旧给药,再给药单次环磷酰胺(150 mg/kg)。实验结束时,我们检测了生化指标:氧化标志物(丙二醛、谷胱甘肽和过氧化氢酶)和肌钙蛋白i,并在光镜和电镜下观察心脏组织的组织病理变化,并利用免疫组织化学技术定位心肌细胞胞质中诱导型一氧化氮合酶(iNOS)。结果显示,与对照组相比,环磷酰胺处理组肌钙蛋白I升高,氧化标志物紊乱。而环磷酰胺和铁皮水芹处理组则明显改善了这些结果。光镜和电镜检查显示,环磷酰胺组心肌组织结构破坏,组织化学检查显示大量心肌细胞胞浆iNOS免疫反应强烈,而环磷酰胺和铁皮毒组心肌细胞恢复到接近正常。综上所述,环磷酰胺具有一定的心脏毒性作用,可通过补充奥officinale加以预防。建议进一步研究环磷酰胺对心脏的毒性作用和巴铁皮草的保护作用。关键词:环磷酰胺;铁皮姜;心脏毒性;
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The possible protective effect of Zingiber officinale extract on cyclophosphamide-induced cardiotoxicity in adult male albino rats
Cyclophosphamide, a cytotoxic alkylating agent, is an extensively used antineoplastic agent. Cardio-toxicity is considered as one of the limiting side effects of its use, which is attributed to oxidative stress. Zingiber officinale is powerful antioxidants against free radicals and oxidative attacks. The aim of this study is to investigate the possible protective effects of Z. officinale against cyclophosphamide induced cardio-toxicity in adult male albino rats. We used 30 adult male albino rats, divided into five groups; Group Ia (-ve control), Group Ib (+ve control), Group II (Z. officinale treated group; 200 mg/kg/day orally), Group III (cyclophosphamide treated group; single dose of 150 mg/kg I.P.), and Group IV (cyclophosphamide and Z. officinale treated group; rats received Z. officinale as before followed by single dose of cyclophosphamide (150 mg/kg)). At the end of experiment, we studied biochemical parameters: oxidative markers (MDA, GSH and Catalase), and Troponin i. The heart tissue was examined by light and electron microscope to evaluate histo-pathological changes and immune-histochemical technique for localization of inducible nitric oxide synthase (iNOS) in the cytoplasm of cardiomyocytes. The result showed increase in troponin I and disturbance of oxidative markers in cyclophosphamide treated group compared to control groups. Whereas these results had significantly improved in cyclophosphamide and Z. officinale treated group. Light and electron microscopic examination revealed disruption in the heart tissue histo-architecture in cyclophosphamide group with strong positive cytoplasmic iNOS immunoreaction in numerous cardiomyocytes by histochemical examination unlike that in cyclophosphamide and Z. officinale treated group which returned near normal. In conclusion, cyclophosphamide has a cardiotoxic effect which can be prevented by Z. officinale supplementation. Further studies about cyclophosphamide toxic effect on the heart and about Z. officinale role in protection are recommended. Key words: Cyclophosphamide, Zingiber officinale, cardiotoxicty.
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