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GC-MS Analysis and Gastroprotective Evaluations of Crude Extracts Isolated Saponins and Essential Oil from Polygonum hydropiper L.

机译:虎杖粗提取物分离的皂苷和精油的GC-MS分析和胃保护性评估。

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摘要

Peptic ulceration is among the most prevalent gastrointestinal disorders characterized by pepsin and gastric acid mediated mucosal damage, as result of imbalance between defensive and offensive processes. The main objective of the current study was to investigate the antiulcer potentials of Polygonum hydropiper crude methanolic ectract (Ph.Cr) in aspirin induced ulcerogenesis using pylorus ligated rat model. In-vitro urease and Proteus mirabilis inhibitory potentials were evaluated using standard protocols. All fractions were analyzed using GC-MS to identify major components. The aspirin induced ulcerogenesis in pylorus ligated rat model was associated with significant changes in the mean ulcer score [F(5, 30) = 7.141, P = 0.0002], gastric juice volume [F(5, 30) = 8.245, P < 0.0001], gastric juice pH [F(5, 30) = 5.715, P = 0.0008], free acidity [F(5, 30) = 4.544, P = 0.0033], total acidity [F(5, 30) = 2.740, P = 0.0373], and pepsin concentration [F(5, 30) = 2.335, P = 0.0664]. Pre-treatment with Ph.Cr at 100, 200, and 400 mg/kg dose exhibited marked gastroprotective and anti-ulcerogenic effect in the aspirin induced pyloric ligation ulcerogenesis model at 100, 200, and 400 mg/kg as indicated by ulcerative biochemical parameters. In urease inhibition assay, leaves essential oil (Ph.Lo), saponins (Ph.Sp), and chloroform extract (Ph.Chf) exhibited highest activities with IC50 of 90, 98, and 520 μg/ml, respectively. Ph.Sp, Ph.Chf, ethyl acetate (Ph.EtAc), and Ph.Cr showed MICs of 25, 30, 32.25, and 40.50 μg/ml, respectively against P. mirabilis. Several compounds were identified in GC-MS analysis of samples. Significant in-vivo antiulcer, urease inhibitory as well as anti-proteus potentials of P. hydropiper solvent extracts, signify its potential use for the management of peptic ulcers and may provide scientific bases for the traditional uses of the plant.
机译:消化性溃疡是最常见的胃肠道疾病之一,其特征是胃蛋白酶和胃酸介导的粘膜损伤,是防御和进攻过程之间不平衡的结果。本研究的主要目的是使用幽门结扎大鼠模型研究何首乌粗甲醇提取物(Ph.Cr)在阿司匹林诱导的溃疡发生中的抗溃疡潜力。使用标准方案评估了体外脲酶和奇异变形杆菌的抑制潜力。使用GC-MS分析所有馏分以鉴定主要成分。阿司匹林在幽门结扎大鼠模型中诱导的溃疡发生与平均溃疡评分[F(5,30)= 7.141,P = 0.0002],胃液量[F(5,30)= 8.245,P <0.0001 ],胃液pH值[F(5,30)= 5.715,P = 0.0008],游离酸度[F(5,30)= 4.544,P = 0.0033],总酸度[F(5,30)= 2.740,P = 0.0373],胃蛋白酶浓度[F(5,30)= 2.335,P = 0.0664]。如溃疡性生化参数所示,在100、200和400 mg / kg的阿司匹林诱导的幽门结扎性溃疡发生模型中,以100、200和400 mg / kg的Ph.Cr预处理显示出显着的胃保护和抗溃疡作用。在脲酶抑制试验中,叶片精油(Ph.Lo),皂苷(Ph.Sp)和氯仿提取物(Ph.Chf)表现出最高的活性,IC50分别为90、98和520μg/ ml。 Ph.Sp,Ph.Chf,乙酸乙酯(Ph.EtAc)和Ph.Cr分别显示出25、30、32.25和40.50μg/ ml的对恶性疟原虫的MIC。在样品的GC-MS分析中鉴定了几种化合物。 P的显着体内抗溃疡,尿素酶抑制作用和抗蛋白水解潜能。 Hydropiper 溶剂提取物,表明其在消化性溃疡管理中的潜在用途,并可能为植物的传统用途提供科学依据。

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