迷迭香提取物减轻雄性大鼠依托泊苷肝、肾毒性的生化和分子研究

Majd Almakhatreh, Ezar H. Hafez, E. Tousson, A. Masoud
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引用次数: 13

摘要

目的:依托泊苷(Vepesid)是一种抑制拓扑异构酶II活性的化疗药物,长期用于治疗人类恶性肿瘤,它是一种半合成化合物,来源于植物Podophyllum peltatum。本研究旨在探讨迷迭香提取物对足泊苷所致大鼠肝肾功能改变及DNA损伤的保护作用。材料与方法:将50只雄性Wistar白化大鼠随机分为4组(1组为对照组;第2组给予迷迭香治疗,第3组给予依托泊苷治疗,第4、5组分别为联合治疗组和后治疗组)。结果:给药后血清ALT、AST、ALP、肌酐、尿素、钾离子、氯离子及DNA损伤显著升高。相比之下;与对照组相比,蛋白、总蛋白、钠离子、钙离子含量显著降低。当迷迭香与乙酰基苷(G4)共处理后,ALT、AST、ALP、肌酐、尿素、钾离子、氯离子增加,DNA损伤减少,或在乙酰基苷(G5)后处理4周,G4损伤最低。此外,迷迭香与鲸乙苷(G4)共处理后,蛋白、总蛋白、钠离子和钙离子的减少增加,或在鲸乙苷(G5)后处理4周,G4损伤最小。结论:迷迭香对依托泊苷化疗所致的肝、肾毒性具有一定的保护作用,值得作为一种天然物质加以考虑。
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Biochemical and Molecular Studies on the Role of Rosemary (Rosmarinus officinalis) Extract in Reducing Liver and Kidney Toxicity Due to Etoposide in Male Rats
Aims: Etoposide (Vepesid) is chemotherapeutic drugs that inhibit topoisomerase II activity and long been used for treatment of human malignancies, where it is a semi-synthetic compound derived from the plant Podophyllum peltatum. The current study was designed to investigate the possible protective effect of rosemary extract against Etoposide -induced changes in liver and kidney functions, and DNA damage in rats. Materials and Methods: A total of 50 male Wistar albino rats were divided randomly into four groups (1st group was control; 2nd group was treated with rosemary, 3rd group was received etoposide, and 4th & 5th groups was co- and post treated groups respectively). Results: The administration of Etoposide revealed a significant increase in serum ALT, AST, ALP, creatinine, urea, potassium ions, chloride ions, and DNA damage. In contrast; a significant decrease in albumen, total proteins, sodium ions, and calcium ions were when compared with control group. This increased in ALT, AST, ALP, creatinine, urea, potassium ions, chloride ions, and DNA damage was reduced after administration of rosemary when co-treated with etoposide (G4), or post-treated after etoposide  (G5) for four weeks with lowest damage in G4. Also, this decreased in albumen, total proteins, sodium ions, and calcium ions was increased after administration of rosemary when co-treated with etoposide (G4), or post-treated after etoposide (G5) for four weeks with lowest damage in G4. Conclusion: It could be concluded that rosemary has a promising role and it worth to be considered as a natural substance for protective the liver and kidney toxicity induced by etoposide (Vepesid) chemotherapy.
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