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Cecropia pachystachya: A Species with Expressive In Vivo Topical Anti-Inflammatory and In Vitro Antioxidant Effects

机译:Cecropia pachystachya:具有表达体内局部抗炎和体外抗氧化作用的物种

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摘要

Cecropia pachystachya is a species traditionally used in Brazil to treat inflammation. This work aims to evaluate the topical anti-inflammatory and antioxidant activities of the methanolic extract of C. pachystachya (CPM) and to perform its chemical fingerprint by HPLC-DAD. The topical anti-inflammatory activity was evaluated using the mouse models of acute ear inflammation induced by croton oil, arachidonic acid, capsaicin, EPP, phenol, and chronic inflammation induced by multiple application of croton oil. The in vitro antioxidant effect of CPM was investigated using DPPH, reducing power, β-carotene bleaching, and TBARS assays. HPLC analysis was performed to quantify the antioxidant phenolics orientin, isoorientin, and chlorogenic acid previously identified in CPM. CPM exhibited significant anti-inflammatory effect in the acute models, in some cases comparable to the reference drugs. Histopathological analysis showed a moderate chronic skin anti-inflammatory effect with decrease in vasodilation, edema, cell infiltration, and epidermal hyperproliferation. It also showed strong in vitro antioxidant activity. The contents of orientin, isoorientin, and chlorogenic acid were 66.5 ± 1.8, 118.8 ± 0.7, and 5.4 ± 0.2 µg/mg extract, respectively. The topical anti-inflammatory activity of CPM could be based on its antioxidant properties, although other effects are probably involved, including COX inhibition and other mechanisms.
机译:Cecropia pachystachya是巴西传统上用于治疗炎症的物种。这项工作的目的是评估厚朴梭菌(CPM)甲醇提取物的局部抗炎和抗氧化活性,并通过HPLC-DAD进行化学指纹分析。使用巴豆油,花生四烯酸,辣椒素,EPP,苯酚引起的急性耳部炎症小鼠模型和巴豆油多次应用引起的慢性炎症模型评估局部抗炎活性。使用DPPH,还原能力,β-胡萝卜素漂白和TBARS分析研究了CPM的体外抗氧化作用。进行HPLC分析以量化先前在CPM中鉴定的抗氧化剂酚类Orientin,isoorientin和绿原酸。 CPM在急性模型中表现出显着的抗炎作用,在某些情况下可与参考药物相比。组织病理学分析显示出中等程度的慢性皮肤抗炎作用,血管扩张,水肿,细胞浸润和表皮过度增殖减少。它还显示出强大的体外抗氧化活性。 Orientin,异Orientinin和绿原酸的含量分别为66.5%±1.8、118.8±0.7和5.4±0.2μg/ mg。 CPM的局部抗炎活性可以基于其抗氧化特性,尽管可能涉及其他作用,包括抑制COX和其他机制。

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