氧化锌纳米颗粒对雄性白化大鼠环磷酰胺血液毒性的改善作用

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引用次数: 2

摘要

背景:环磷酰胺(CP)是一种临床应用广泛的药物。氧化锌是应用最广泛的纳米颗粒。纳米颗粒可以诱导氧化应激,最终导致细胞毒性、炎症和溶血。目的:研究锌- o纳米颗粒和/或环磷酰胺对雄性大鼠血液学的影响。材料与方法:将24只成年雄性大鼠(Sprague Dawley)随机分为4组,每组6只。ⅰ组:对照组:0.2 ml生理盐水/天腹腔注射,连续14天(逐日);ⅱ组(CP组):每日给予CP 20 mg/kg/天体重(体重)腹腔注射,连续14天;ⅲ组(nZnO组):每日给予nZnO 5 mg/kg/天体重,连续14天。IV组(CP + ZnO NPs组):给予nZnO (5 mg/kg/day) bw腹腔注射,连续14 d,再加CP 20mg/kg/day体重(bw),逐日腹腔注射,连续14 d。实验结束时,用光醚麻醉大鼠。采集血样进行血液学评估。结果:与对照组相比,CP组大鼠红细胞计数、血红蛋白浓度、白细胞计数明显下降,nZnO联合CP组大鼠红细胞和血红蛋白值变化明显减轻。与对照组相比,cp免疫抑制组中性粒细胞、淋巴细胞、嗜酸性粒细胞和单核细胞计数明显减少。在CP免疫抑制的动物中,与CP处理组相比,这些参数得到改善。结论:CP可引起血液学指标的改变。纳米氧化锌颗粒与CP联合治疗大鼠,可明显改善CP的毒性,为改善化疗毒副反应、合理治疗提供参考。然而,需要进一步的研究来确定nZnO的最佳剂量并获得最佳的安全性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ameliorating Effect of Zinc Oxide Nanoparticles against Hematotoxicity Induced by Cyclophosphamide in Male Albino Rats
Background: Cyclophosphamide (CP) is a drug with a wide spectrum of clinical uses. Zinc oxide is the most widely used nanoparticles. Nanoparticles could induce oxidative stress that eventually leads to cell toxicity, inflammation and hemolysis. Objectives: The objective of this study was to evaluate the hematological changes induced by Zn-O nano-particles and/or Cyclophosphamide in male rats. Materials and Methods: Twenty four adult male rats (Sprague Dawley) were grouped randomly into four groups of six rats each. Group I. Control group: Received 0.2 ml saline /day i.p. injection for 14 days (day by day), group II (CP group): Received CP 20 mg/kg/day body weight (b.w.) day by day for 14 days by intraperitoneal injection, Group III (nZnO group): Received nZnO (5 mg/kg)/day b.w., intraperitoneally for 14 days. Group IV (CP + ZnO NPs group): Received nZnO group: Received nZnO (5 mg/kg/day) b.w., intraperitoneally for 14 days, plus CP 20mg/kg/day body weight (b.w.) day by day for 14 days by intraperitoneal injection. At the end of the experimental period, rats were anesthetized using light ether. Blood samples were taken for hematological evaluation. Results: Red blood cells count, hemoglobin concentration, and white blood cells count were significantly decline in rats treated with CP in comparison to control group, while combination of nZnO with CP reduced changes in red bood cells and hemoglobin values. Neutrophils, lymphocytes, eosinophils, and monocytes count were significantly decreased in CP-immunosuppressed group when compared with the control group. In CP-immunosuppressed animals treated with nZnO, these parameters were improved when compared with CP treated groups. Conclusion: It can be concluded that CP induced changes in the hematological parameters. Treatment of rats with zinc oxide nano-particles and CP together ameliorated the toxicity induced by CP. These results may provide further visions into proper treatment of patients by improving side effects of chemotheraby. However further studies are necessary to establish optimal doses of nZnO and receive the best safety profile.
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