槲皮素和水飞蓟素的胶囊剂及其组合对二甲基亚硝胺诱导和苯巴比妥促进的大鼠肝细胞癌模型的影响

Devendra S Shirode, Dinesh J Raut, Nikita Sarasawat
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引用次数: 0

摘要

背景:肝细胞癌是一种特别危险和严重的肝癌:肝细胞癌是一种特别危险和严重的肝癌。许多抗癌药物都无法完成对肝细胞癌的无副作用治疗。肝细胞癌应该有合适且无副作用的治疗方法:本研究的目的是评估含槲皮素和水飞蓟素的口服制剂对由二乙基亚硝胺引起的肝细胞癌的影响:方法:30 只雄性大鼠分为五组。正常对照组(未治疗组)、肿瘤组(二甲基亚硝胺 200 毫克/千克)、治疗 I 组(槲皮素胶囊 50 毫克/千克)、治疗 II 组(水飞蓟素胶囊 50 毫克/千克)和治疗 III 组(槲皮素胶囊 + 水飞蓟素胶囊 50 毫克/千克)。然后进行生化测定、血清分析和组织病理学检查:结果:采用 50 毫克/千克槲皮素和水飞蓟素组合胶囊治疗的第三组显示,甲胎蛋白和癌胚抗原以及超氧化物歧化酶和一氧化氮等抗氧化剂均显著恢复。组织病理学检查显示,与其他治疗组相比,该组的肝脏结构有所改善:我们的研究结果表明,在治疗组 III 中观察到了有效的抗癌效果,因为乳糖配方提高了药物在体内的生物利用率。为了全面了解这些化学物质治疗肝细胞癌的基本过程并评估其疗效,还需要进一步的调查和临床试验。
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Effect of Niosomal Encapsulation of Quercetin and Silymarin and their Combination on Dimethylnitrosoamine-induced and Phenobarbital promoted Hepatocellular Carcinoma in Rat Model.

Background: Hepatocellular carcinoma is a particularly dangerous and severe kind of liver cancer. Many anticancer drugs fail to complete the treatment of hepatocellular carcinoma without any side effects. There should be appropriate and without side effective treatments for hepatocellular carcinoma.

Objective: The objective of the current study was to evaluate how quercetin and silymarin in a niosomal formulation affected hepatocyte carcinoma caused by diethylnitrosamine.

Methods: Five groups were created from the thirty male rats. Normal control (untreated group), tumor group (administered dimethylnitrosoamine 200 mg/kg), treatment group I (administered 50 mg/kg of niosomal encapsulated quercetin), treatment group II (administered 50 mg/kg of niosomal encapsulated silymarin), and treatment group III (administered 50 mg/kg of niosomal encapsulated quercetin + silymarin). Then, biochemical estimation, serum analysis, and histopathological examination were carried out.

Results: Treatment group III, treated with niosomal encapsulation of a combination of quercetin + silymarin 50 mg/kg, demonstrated the significant restoration of alpha-fetoprotein and carcinoembryonic antigen and also antioxidants like superoxide dismutase and nitric oxide. The histopathological examination showed improved liver architecture in this group compared to other treatment groups.

Conclusion: Our findings revealed that a potent anticancer effect was observed in treatment group III as niosomal formulation increased the bioavailability of the drug within the body. In order to completely understand the underlying processes and evaluate the therapeutic effectiveness of these chemicals in the therapy of hepatocellular carcinoma, further investigation and clinical trials are required.

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