Pharmacological Investigation on Unraveling Mechanism of Action of Qusqualis indica Leaves for Predicted Treatment of Peptic Ulcer Disease

M. Kulshreshtha, Rajaneesh Kumar Chaudhary, Supriya Roy, Karuna Shanker Shukla, Anita Singh, Manjul Pratap Singh
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引用次数: 3

Abstract

With the aid of various ulcer-induced models, the goal of this study was to assess the antiulcer ability of Qusqualis indica (Q. indica) leaf extracts in Wistar rats The induction of ulcers was done by different models like pylorus ligation method, ethanol-induced and stress-induced models. Group 1 (negative control), Group 2 (standard group) were treated with Sucralfate (8.6 mg/kg), Group 3 was treated with aqueous extract of Q. indica (AEQI,200 mg/kg), Group 4 was treated with aqueous extract of Q. indica (AEQI,400 mg/kg), Group 5 was treated with ethanolic extract of Q. indica (EEQI, 200 mg/kg) and Group 6 was treated with ethanol extract of Q. indica (EEQI, 400 mg/kg). All therapies were given orally twice every day. After the course of treatment was complete, blood and gastrointestinal contents were taken, and biochemical tests were run. The acetylcholine and histamine drug response curves were used to develop the mechanism of the extracts. The groups treated with extracts experienced a significant decrease in ulcer index. The antiulcer potential of the AEQI and EEQI is dose-dependent. Hematological, hepatic, and cardiac parameters were not significantly affected by the extracts, although high-density lipoprotein production was. Acetylcholine and histamine are blocked by AEQI and EEQI, according to the DRC analysis. The obtained scientific facts are amply supported by histopathological analysis AEQI and EEQI have antiulcer potential in a dose-dependent manner, but further research must be needed.
黄芪叶预测治疗消化性溃疡作用机制的药理研究
本研究采用幽门结扎法、乙醇诱导模型和应激诱导模型对大鼠进行溃疡诱导,并通过多种溃疡诱导模型对大鼠的抗溃疡能力进行评价。1组(阴性对照)、2组(标准组)采用硫硫酸盐(8.6 mg/kg)处理,3组采用青芪水提物(AEQI,200 mg/kg)处理,4组采用青芪水提物(AEQI,400 mg/kg)处理,5组采用青芪乙醇提物(EEQI, 200 mg/kg)处理,6组采用青芪乙醇提物(EEQI, 400 mg/kg)处理。所有治疗方法均为每日口服2次。疗程结束后,抽血和胃肠道内容物,并进行生化检查。采用乙酰胆碱和组胺药物反应曲线研究其作用机理。用提取物治疗组溃疡指数明显降低。AEQI和EEQI的抗溃疡潜能是剂量依赖性的。血液学、肝脏和心脏参数没有受到提取物的显著影响,尽管高密度脂蛋白的产生受到了影响。根据DRC的分析,乙酰胆碱和组胺被AEQI和EEQI阻断。所获得的科学事实得到组织病理学分析的充分支持,aeqi和EEQI具有剂量依赖性的抗溃疡潜力,但仍需进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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