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首页> 外文期刊>Oriental pharmacy and experimental medicine >In vitro antimicrobial activity study and in vivo antiemetic, antinociceptive activity evaluation of leaves extract of Erioglossum rubiginosum using experimental animal model
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In vitro antimicrobial activity study and in vivo antiemetic, antinociceptive activity evaluation of leaves extract of Erioglossum rubiginosum using experimental animal model

机译:利用实验动物模型对风信子叶片提取物的体外抗菌活性及体内止吐,止痛活性评价

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The present study explored the phytochemical screening, in vitro antimicrobial activity, in vivo antiemetic and antinociceptive potentialities of methanol extract of Erioglossum rubiginosum leaves for the first time. Crude extract of E. rubiginosum and different fractions were assayed for in vitro antimicrobial activity using disc diffusion method. The antiemetic activity was evaluated using chick emesis model; while acetic acid induced writhing test in mice was conducted to determine the antinociceptive activity. Different extracts possess carbohydrate, flavonoids, saponin, tannin, alkaloids, phenol and cardiac-glycoside in varying concentrations. Among different extractives, only the chloroform soluble fraction showed promising antimicrobial activity (zone of inhibition 6.5 to 10 mm) in comparison to positive control?ciprofloxacin, against wide range of tested microorganisms. In antiemetic assay, all the extracts showed significant (P < 0.05) activities; among them both chloroform and carbon tetrachloride extracts showed better activity (inhibition 91 and 90 % respectively) compared to the standard drug metoclopramide (inhibition 74 %). In antinociceptive assay, remarkable writhing inhibitory activity was found for the chloroform extract (53.05 %), while the standard drug diclofenac sodium inhibited 42.01 % writhing of the test animals (P < 0.05). Therefore, further studies and compound isolation are suggested to confirm the mechanism of the key compounds as the plant extracts of E. rubiginosum revealed potential biological and pharmacological activities.
机译:本研究首次探索了赤桑叶甲醇提取物的植物化学筛选,体外抗菌活性,体内止吐和抗伤害感受能力。利用圆盘扩散法测定了茜草和不同级分的粗提物的体外抗菌活性。使用雏鸡呕吐模型评估止吐活性;同时用乙酸诱导小鼠扭体试验以确定其抗伤害感受活性。不同的提取物具有不同浓度的碳水化合物,类黄酮,皂苷,单宁,生物碱,苯酚和强心苷。在不同的提取物中,与阳性对照环丙沙星相比,只有氯仿可溶级分显示出有希望的抗微生物活性(抑制范围为6.5至10 mm),对多种受试微生物具有抗微生物活性。在止吐试验中,所有提取物均表现出显着的活性(P <0.05);其中氯仿和四氯化碳提取物均比标准药物甲氧氯普胺(抑制74%)表现出更好的活性(抑制作用分别为91和90%)。在抗伤害感受试验中,发现氯仿提取物具有明显的扭体抑制活性(53.05%),而标准药物双氯芬酸钠则抑制了测试动物的扭体(42.01%)(P <0.05)。因此,建议进一步研究和化合物分离以确认关键化合物的作用机理,因为茜草E. rubiginosum的植物提取物显示出潜在的生物学和药理活性。

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