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首页> 外文期刊>International Journal of Pharmacy and Pharmaceutical Sciences >POTENTIAL ANTIOXIDANT, ANTI-INFLAMMATORY AND ANTIBACTERIAL EVALUATION OF EXTRACTS OF LEUCAS ASPERA USING IN VITRO MODELS
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POTENTIAL ANTIOXIDANT, ANTI-INFLAMMATORY AND ANTIBACTERIAL EVALUATION OF EXTRACTS OF LEUCAS ASPERA USING IN VITRO MODELS

机译:体外模型对潜在的抗氧化剂,白术提取物的抗炎和抗菌评价

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Objective: To evaluate the potential antioxidant, anti-inflammatory and antibacterial activities of aqueous and methanolic extracts of leaves of Leucas aspera (Thumbae). Methods: Phytochemical screening of the leaves of L. aspera was followed by analysis of antioxidant activity by means of DPPH (2, 2-diphenyl-1-picrylhydrazyl) radical scavenging activity. In vitro anti‐inflammatory activity was evaluated using lipoxygenase inhibition, albumin denaturation assay, membrane stabilization assay and proteinase inhibitory activity at different concentrations. Aspirin was used as a standard drug for the study of anti‐inflammatory activity. Linear regression analysis was used to calculate half maximal inhibitory concentration, IC50 value. The zone of inhibition was performed against common pathogens to determine the antimicrobial activity at different concentrations of plant extracts (60%, 70%, 80%). Results: The phytochemical analysis revealed the presence of carbohydrates, amino acid, alkaloids, tannins, flavonoids, glycosides, xanthoproteins, and phenols. The total phenolic and flavonoid content was found to be 2.25±0.04 mg GAE/g (gallic acid equivalents) and 1.2±0.05 mg QE/g (Quercetin equivalents) of fresh weight tissue respectively. The IC50 values for hydrogen peroxide scavenging activity were found to be 244.6 μg/ml. The extract inhibited the lipoxygenase enzyme activity with an IC50 value of 356.3 μg/ml. Maximum inhibition of heat-induced protein denaturation of 69% was observed at 400 μg/ml, IC50 249.6 μg/ml. Proteinase activity was also significantly inhibited (IC50 = 421.6 μg/ml). Membrane stabilization assay attributed minor protection by the leaf extract with an IC50 of 206.7. It was observed that E. coli were inhibited at all concentrations, followed by Klebsiella and Pseudomonas . Conclusion: Results indicate that L. aspera possess anti-inflammatory properties due to the strong occurrence of polyphenolic compounds such as alkaloids, flavonoids, tannins and steroids that serve as free radical inhibitors or scavenger. Compounds of the plant L. aspera may hence be used as lead compounds for designing potent anti-inflammatory drug which can be used for treatment of various diseases.
机译:目的:评价白茅(Leucas aspera)(Thumbae)叶片水和甲醇提取物的潜在抗氧化,抗炎和抗菌活性。方法:通过植物化学筛选法测定了曲霉叶片,然后通过清除DPPH(2,2-二苯基-1-吡啶并肼基)自由基的活性来分析其抗氧化活性。使用脂氧合酶抑制,白蛋白变性测定,膜稳定测定和不同浓度的蛋白酶抑制活性评估了体外抗炎活性。阿司匹林被用作研究抗炎活性的标准药物。线性回归分析用于计算最大抑制浓度的一半,IC50值。对常见病原体进行抑制区以确定在不同浓度的植物提取物(60%,70%,80%)下的抗菌活性。结果:植物化学分析表明存在碳水化合物,氨基酸,生物碱,单宁,类黄酮,糖苷,黄体蛋白和酚。发现新鲜重量组织的总酚和类黄酮含量分别为2.25±0.04 mg GAE / g(没食子酸当量)和1.2±0.05 mg QE / g(槲皮素当量)。发现过氧化氢清除活性的IC 50值为244.6μg/ ml。提取物抑制脂氧合酶活性,IC50值为356.3μg/ ml。在400μg/ ml,IC50 249.6μg/ ml处观察到对热诱导蛋白质变性的最大抑制为69%。蛋白酶活性也被显着抑制(IC50 = 421.6μg/ ml)。膜稳定化验归因于叶提取物的保护作用较弱,IC50为206.7。观察到大肠杆菌在所有浓度下均被抑制,其次是克雷伯菌和假单胞菌。结论:结果表明,由于多种有机酚类化合物(如生物碱,类黄酮,丹宁和类固醇)作为自由基抑制剂或清除剂的大量存在,因此具有抗炎作用。因此,植物曲霉的化合物可用作设计有效的抗炎药的先导化合物,所述抗炎药可用于治疗各种疾病。

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