Department of Pharmaceutical and Biomedical Sciences, University of Salerno, Fisciano, Salerno, Italy.
J Ethnopharmacol. 2011 Dec 8;138(3):705-12. doi: 10.1016/j.jep.2011.09.056. Epub 2011 Oct 6.
The genus Paeonia (Paeoniaceae), is one of the most important source of crude drugs in traditional Chinese medicine and investigation on many species is large. Up to now studies on Paeonia rockii, one of the eight species recognized in the section Moutan, are very limited.
This research aimed to investigate the composition of Paeonia rockii roots and to evaluate the in vitro free-radical scavenging and antifungal activities of a polar extract (PPR) and its major constituents.
PPR was obtained from defatted dried roots of Paeonia rockii using MeOH as extraction solvent. Its n-BuOH soluble portion (PPR-B) was purified by Sephadex LH-20 followed by RP-HPLC to give nineteen compounds belonging to the classes polyphenols, monoterpenes and triterpenes. Their structure were spectrally characterized (UV, 1D and 2D NMR, MS). The polyphenols content of PPR and PPR-B was examined by the Folin-Ciocalteau colorimetric assay and HPLC method. Both extracts (PPR and PPR-B) and their major constituents were tested for the free-radical scavenging activity by DPPH-test, and for the antifungal activity by three methods (micro-broth dilution method, XTT assay and Candida albicans morphological analysis).
5-Butylhydroxy-γ-lactone (1), and ethyl-arabinopyranoside (2) have been isolated for the first time as naturally occurring compounds and taxifolin (3) was reported for the first time in Paeonia spp. Nine polyphenols, four monoterpenes and three triterpenes were also identified. Both the extracts PPR and PPR-B had high polyphenol content, and high concentration of gallic acid derivatives and paeoniflorin, chemotaxonomic characteristic markers of the genus. PPR, gallic acid and methyl-gallate displayed high potency in scavenging free-radicals (DPPH test, EC(50) 13.3, 1.2, 1.9 μg/ml, respectively). Both the extracts and gallic acid individually showed an interesting antifungal property (MIC(50) at 24 h 25, 0.9 and 30 μg/ml, respectively) and notably, a combination of paeoniflorin/gallic acid (MIC(50)=0.5+20 μg/ml, respectively) was more active than the single compound in inhibiting Candida growth.
The polar methanolic extract (PPR), its n-BuOH soluble fraction and constituents of Paeonia rockii were extensively investigated. Both extracts and some of their compounds have the ability to scavenge free-radicals and to inhibit Candida albicans growth.
芍药属(芍药科)是中药最重要的天然药物来源之一,对许多物种的研究都很多。迄今为止,对牡丹组中被识别的八个物种之一的牡丹石碱的研究非常有限。
本研究旨在研究牡丹石碱根的组成,并评价极性提取物(PPR)及其主要成分的体外自由基清除和抗真菌活性。
用甲醇作为提取溶剂,从牡丹石碱脱脂干燥根中提取 PPR。其正丁醇可溶部分(PPR-B)通过 Sephadex LH-20 纯化,然后通过 RP-HPLC 得到属于多酚、单萜和三萜类的十九种化合物。通过光谱(UV、1D 和 2D NMR、MS)对其结构进行了表征。通过 Folin-Ciocalteau 比色法和 HPLC 方法检查 PPR 和 PPR-B 的多酚含量。用 DPPH 试验测试两种提取物(PPR 和 PPR-B)及其主要成分的自由基清除活性,用三种方法(微量肉汤稀释法、XTT 测定法和白色念珠菌形态分析)测试抗真菌活性。
5-丁基羟基-γ-内酰胺(1)和乙基阿拉伯吡喃糖苷(2)首次作为天然存在的化合物分离,而杨梅素(3)首次在芍药属中报道。还鉴定了九种多酚、四种单萜和三种三萜。提取物 PPR 和 PPR-B 均具有较高的多酚含量,且含有高浓度的没食子酸衍生物和芍药苷,这是该属的化学分类特征标记物。PPR、没食子酸和甲基没食子酸在清除自由基(DPPH 试验,EC(50)分别为 13.3、1.2 和 1.9μg/ml)方面表现出高活性。两种提取物和没食子酸单独表现出有趣的抗真菌特性(24 小时 MIC(50)分别为 25、0.9 和 30μg/ml),值得注意的是,芍药苷/没食子酸的组合(MIC(50)=0.5+20μg/ml)比单一化合物更能抑制白色念珠菌的生长。
对芍药石碱的极性甲醇提取物(PPR)、其正丁醇可溶部分及其成分进行了广泛研究。两种提取物及其一些化合物具有清除自由基和抑制白色念珠菌生长的能力。