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从智利蓝珀仙人掌(Mart. ex Pfeiff.)中分离得到的奇卡佩根、peniocerol 和 macdougallin 的抗炎和细胞毒性活性

Anti-inflammatory and cytotoxic activities of chichipegenin, peniocerol, and macdougallin isolated from Myrtillocactus geometrizans (Mart. ex Pfeiff.) Con.

机构信息

Instituto de Química, Universidad Nacional Autónoma de México, Ciudad Universitaria, Circuito Exterior, Coyoacán, C. P. 04510, México, D. F., México.

出版信息

Z Naturforsch C J Biosci. 2011 Jan-Feb;66(1-2):24-30.

Abstract

The oleanane-type triterpene chichipegenin and the sterols peniocerol and macdougallin, isolated from Myrtillocactus geometrizans, showed anti-inflammatory activities in both the 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced mouse ear edema model and the carrageenan-induced rat paw edema model. All tested compounds inhibited the TPA-induced edema in a dose-dependent manner, with ED50 values less than or equal to that shown by indomethacin. Among them, peniocerol was the most active compound. However, only peniocerol and macdougallin reduced carrageenan-induced rat paw edema. On the other hand, peniocerol and macdougallin showed cytotoxicity against several human cancer cell lines. These results indicate that compounds isolated from M. geometrizans possess antiinflammatory and cytotoxic properties, and the presence of chichipegenin in the aerial parts could justify the medicinal uses attributed to the plant.

摘要

从智利酒椰中分离得到的齐墩果烷型三萜齐墩果酸和甾体化合物松柏甾醇、麦角甾醇具有抗炎活性,在十四酰佛波醇-13-乙酸酯(TPA)诱导的小鼠耳肿胀模型和角叉菜胶诱导的大鼠足肿胀模型中均表现出抗炎活性。所有测试的化合物均以剂量依赖的方式抑制 TPA 诱导的水肿,半数有效剂量(ED50)小于或等于吲哚美辛。其中,松柏甾醇活性最强。然而,只有松柏甾醇和麦角甾醇能减轻角叉菜胶诱导的大鼠足肿胀。另一方面,松柏甾醇和麦角甾醇对几种人癌细胞系具有细胞毒性。这些结果表明,从 M. geometrizans 中分离得到的化合物具有抗炎和细胞毒性作用,智利酒椰地上部分含有齐墩果酸可能解释了该植物的药用价值。

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