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Anti-inflammatory effects in muscle injury by transdermal application of gel with Lychnophora pinaster aerial parts using phonophoresis in rats

机译:凝胶透皮肌损伤中肌肉损伤的抗炎作用用大鼠致癌血清酚的肺炎洛拉·皮诺斯特空中零件

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Background Lycnophora pinaster is used by the traditional Brazilian medicine for the treatment of inflammations. Anti-inflammatory activity of Lycnophora pinaster was investigated for extracts, fractions, and isolated compounds of their aerial parts. The hexane extract (HE) provided α-amyrin, lupeol, mixture of α-amyrin and lupeol, mixture of 3-O-acetyl-lupeol and 3-O-acetyl-pseudotaraxasterol, and mixture of the steroids stigmasterol and sitosterol. The aqueous extract (WE) provided a fraction containing alkaloids (AF) and another one containing phenolic compounds (PF). Methods The crude hexane extract obtained from aerial parts of L. pinaster was submitted to chromatographic fractionation. The fractionation of PF was performed by preparative HPLC analysis, providing the flavonoid quercetin. The extracts, fractions, and compounds isolated from L. pinaster were tested to evaluate the anti-inflammatory activity by experimental model of impact injury, followed by transdermal application of gels with these samples. The application of the gels was performed using phonophoresis in rat paws after induction of muscle injury. Histological analysis was based on scores assigned by the capacity of decreasing the lesion. Results HE and WE exhibited anti-inflammatory activity. Some fractions, triterpenes, and steroids also reduced the inflammatory infiltrates caused by muscle injury. Lupeol promoted a significant reduction of inflammation. Quercetin also provided significant results, promoting the greatest decreases in muscle injury. Conclusion The results of this work suggest that topical application of triterpenes, steroids and flavonoid significantly decreases the inflammatory process generated by muscle injury. The transdermal application using phonophoresis in rat paws of gel with lupeol and quercetin attenuates the inflammation.
机译:背景LycNophora Pinaster被传统的巴西药物用于治疗炎症。研究了LycNophora Pinaster的抗炎活性,用于提取物,级分和分离的它们的空中零件化合物。己烷提取物(He)提供α-氨醇,碱基,α-奥霉素和碱的混合物,3-O-乙酰基 - 卢克酚的混合物和3-O-乙酰基-PseudotaroLol,以及类固醇的混合物Stigmasterol和Sitososterol。水性提取物(我们)提供含有生物碱(AF)的级分,另一个含有酚类化合物(PF)。方法从L. Pinaster的空中部位获得的粗己烷提取物提交给色谱分级。通过制备型HPLC分析进行PF的分馏,提供类黄酮槲皮素。检测从L. Pinaster中分离的提取物,级分和化合物以通过冲击损伤的实验模型评价抗炎活性,然后用这些样品透皮施加凝胶。在诱导肌肉损伤后,在大鼠爪子中使用血管素进行凝胶的施用。组织学分析基于通过减少病变的能力分配的分数。结果他和我们表现出抗炎活动。一些级分,三萜和类固醇也降低了由肌肉损伤引起的炎症渗透。 Lupeol促进了炎症的显着减少。槲皮素还提供了显着的结果,促进肌肉损伤的最大降低。结论这项工作的结果表明,Triterpenes,类固醇和黄酮类化合物的局部应用明显降低了肌肉损伤产生的炎症过程。使用Lupeol和槲皮素在凝胶的大鼠爪中使用致癌术的透皮施用衰减炎症。

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