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Anti-inflammatory effects of methyl ursolate obtained from a chemically derived crude extract of apple peels: potential use in rheumatoid arthritis.

机译:从化学衍生的苹果皮粗提取物中获得的熊果酸甲酯的抗炎作用:在类风湿性关节炎中的潜在用途。

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摘要

Ursolic acid (UA), a pentacyclic triterpene acid found in apple peels (Malus domestica, Borkh, Rosaceae), has a large spectrum of pharmacological effects. However, the vegetal matrix usually produces highly viscous and poorly soluble extracts that hamper the isolation of this compound. To overcome this problem, the crude EtOH-AcOEt extract of commercial apple peels was exhaustively treated with diazomethane, after which methyl ursolate (MU) was purified by column chromatography and characterized spectrometrically. The anti-inflammatory effects of UA and MU (50 mg/kg) were analyzed by zymosan-induced paw edema, pleurisy and in an experimental arthritis model. After 4 h of treatment with UA and MU, paw edema was reduced by 46 and 44 %, respectively. Both UA and MU inhibited protein extravasation into the thoracic cavity; tibio-femoral edema by 40 and 48 %, respectively; and leukocyte influx into the synovial cavity after 6 h by 52 and 73 %, respectively. Additionally, both UA and MU decreased the levels of mediators related to synovial inflammation, such as KC/CXCL-1 levels by 95 and 90 %, TNF-α levels by 76 and 71 %, and IL-1β levels by 57 and 53 %, respectively. Both the compounds were equally effective when assayed in different inflammatory models, including experimental arthritis. Hence, MU may be considered to be a useful anti-inflammatory derivative to overcome the inherent poor solubility of UA for formulating pharmaceutical products.
机译:熊果酸(UAs)是苹果皮中的五环三萜酸(Malus domestica,Borkh,Rosaceae),具有广泛的药理作用。但是,植物基质通常会产生高粘度和难溶的提取物,从而阻碍了该化合物的分离。为克服此问题,将商品苹果皮的粗制EtOH-AcOEt提取物用重氮甲烷彻底处理,然后通过柱色谱法纯化尿嘧啶甲酯(MU),并进行光谱表征。通过酵母聚糖诱导的爪水肿,胸膜炎和实验性关节炎模型分析了UA和MU(50 mg / kg)的抗炎作用。 UA和MU治疗4小时后,足爪水肿分别减少46%和44%。 UA和MU均抑制蛋白质渗入胸腔。胫股水肿分别为40%和48%; 6小时后,白细胞和白细胞流入滑膜腔的比例分别为52%和73%。此外,UA和MU均降低了与滑膜炎症相关的介质水平,例如KC / CXCL-1水平降低了95%和90%,TNF-α水平降低了76%和71%,IL-1β水平降低了57%和53% , 分别。在不同的炎症模型(包括实验性关节炎)中进行分析时,两种化合物均具有同等效力。因此,MU可以被认为是克服UA用于配制药物产品固有的不良溶解性的有用的抗炎衍生物。

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