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Anti-nociceptive Effect of 7-methoxy Coumarin from Eupatorium Triplinerve vahl (Asteraceae)

机译:紫茎泽兰7-甲氧基香豆素的镇痛作用

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Aim: To evaluate the anti-nociceptive activity of 7-methoxy coumarin isolated from ethyl acetate fraction of the alcoholic extract of Eupatorium triplinerve Vahl . Materials and Methods: The shade dried leaves of E. triplinerve were extracted with ethyl alcohol and the extract was condensed. This extract was fractionated with n-hexane, ethyl acetate, and n-butanol. The ethyl acetate fraction was subjected to column chromatography which yielded a crystalline compound-A, which was investigated for spectral characteristics. Pharmacological studies: The isolated compound-A was subjected to behavioral studies and anti-nociceptive evaluation in mice by acetic acid induced writhing and formalin induced nociception. Results: The spectral studies indicated that the structure of compound-A complies with 7- methoxy coumarin. Pre-treatment with 7-methoxy coumarin reduced the number of abdominal constrictions in mice and decreased the time spent in paw licking and biting response in formalin assay. There were no significant behavioral changes. Conclusion: A dose dependent anti-nociceptive action of 7- methoxy coumarin was revealed by the present experiments which support the traditional use of E. triplinerve in pain and inflammatory disorders. SUMMARY Bio-guided fractionation of alcoholic extract of E. triplinerve yielded 7-methoxy coumarin. 7-methoxy coumarin was evaluated for its anti-nociceptive potential by acetic acid induced writhing and formalin induced nociception assays. 7-methoxy coumarin exhibited significant inhibition of acetic acid induced writhing response and the second phase of formalin nociception. The anti-nociceptive action of 7-methoxy coumarin revealed by the present experiments supports the traditional use of E. triplinerve in pain and inflammatory disorders. Open in a separate window.
机译:目的:评价从紫茎泽兰(Eupatoriumtriplinerve Vahl)的醇提取物中的乙酸乙酯级分中分离得到的7-甲氧基香豆素的抗伤害感受活性。材料与方法:用乙醇提取三叶草阴凉干燥的叶子,并将提取物浓缩。将该萃取物用正己烷,乙酸乙酯和正丁醇分级分离。将乙酸乙酯馏分进行柱色谱分离,得到结晶化合物-A,对其进行光谱特性研究。药理学研究:通过乙酸诱导的扭体和福尔马林诱导的伤害感受对分离的化合物A进行了行为研究和抗伤害感受性评估。结果:光谱研究表明化合物-A的结构符合7-甲氧基香豆素。用7-甲氧基香豆素进行的预处理减少了小鼠腹部的收缩次数,并减少了在福尔马林测定中舔足和咬咬反应所花费的时间。没有明显的行为变化。结论:本实验揭示了7-甲氧基香豆素的剂量依赖性抗伤害感受作用,这支持在疼痛和炎性疾病中传统使用曲霉毒素。发明内容曲霉肠球菌的乙醇提取物的生物引导分馏产生7-甲氧基香豆素。通过乙酸诱导的扭体法和福尔马林诱导的伤害感受测定法评价了7-甲氧基香豆素的抗伤害感受能力。 7-甲氧基香豆素表现出对乙酸诱导的扭体反应和福尔马林伤害感受第二阶段的显着抑制作用。本实验揭示的7-甲氧基香豆素的抗伤害感受作用支持曲霉肠球菌在疼痛和炎性疾病中的传统用途。在单独的窗口中打开。

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