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首页> 外文期刊>Journal of Ethnopharmacology: An Interdisciplinary Journal Devoted to Bioscientific Research on Indigenous Drugs >Lignans from the stems of Clematis armandii ('Chuan-Mu-Tong') and their anti-neuroinflammatory activities
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Lignans from the stems of Clematis armandii ('Chuan-Mu-Tong') and their anti-neuroinflammatory activities

机译:铁线莲铁线(“ Chuan-Mu-Tong”)茎中的木质素及其抗神经炎活性

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Ethnopharmacological relevance The dried stems of Clematis armandii (Caulis clematidis armandii), named "Chuan-Mu-Tong" in Chinese Pharmacopoeia, have been traditionally used as an herbal remedy mainly for inflammation-associated diseases. The Aim of the study is to identify the potential anti-neuroinflammatory components from Clematis armandii. Materials and methods The ethanol extract of "Chuan-Mu-Tong" was suspended in H2O and exhaustively extracted with CH2Cl2. The CH2Cl2 fraction was successively subjected to column chromatography (CC) over silica gel, Sephadex LH-20, and semi-preparative HPLC. The structures of the isolated compounds were identified by spectroscopic methods and by comparison with those reported in the literature. Their anti-neuroinflammatory activities were evaluated by inhibitory effects on pro-inflammatory mediators [e.g. nitric oxide (NO) and tumor necrosis factor-alpha (TNF-α)] in lipopolysaccharide (LPS)-activated BV-2 cells. Results One new and sixteen known lignans were isolated and characterized. The absolute configuration of the new lignan, (7R,8S)-9-acetyl-dehydrodiconiferyl alcohol (1), was elucidated by a combination of 1D/2D NMR techniques and the Electronic Circular Dichroism (ECD) spectroscopy based on the empirical helicity rules. The anti-neuroinflammatory bioassay showed that compounds 1, (7R,8S)-dehydrodiconiferyl alcohol (2), erythro-guaiacylglycerol-β- coniferyl ether (5), and threo-guaiacylglycerol-β-coniferyl ether (6) displayed significant inhibitory effects on NO production. Among them, neolignans 1 and 2 exhibited more potent activities than the positive control (NG-monomethyl-l-arginine, l-NMMA), with an IC50 value of 9.3 and 3.9 μM, respectively. Moreover, both 1 and 2 were also found to concentration-dependently suppress the TNF-α release in LPS-stimulated BV-2 cells. Conclusion The results revealed that lignans are the major components of "Chuan-Mu-Tong", and their anti-neuroinflammatory activities strongly support the traditional application of this herb medicine on inflammation. Moreover, the dihydrobenzo[b]furan neolignans 1 and 2 as well as Caulis clematidis armandii could be further exploited as new therapeutic agents to treat inflammation-mediated neurodegenerative and aging-associated diseases.
机译:民族药理学相关性铁线莲的干茎在中国药典中被称为“川木通”,传统上一直用作主要用于治疗炎症相关疾病的草药。该研究的目的是从华铁线莲中鉴定出潜在的抗神经炎成分。材料和方法将“川木桐”乙醇提取物悬浮在H2O中,并用CH2Cl2彻底提取。将CH 2 Cl 2馏分依次在硅胶,Sephadex LH-20和半制备HPLC上进行柱色谱(CC)。分离的化合物的结构通过光谱学方法鉴定,并与文献报道的结构进行比较。通过对促炎性介质的抑制作用来评估它们的抗神经炎活性[例如。一氧化氮(NO)和肿瘤坏死因子-α(TNF-α)]在脂多糖(LPS)激活的BV-2细胞中。结果分离并鉴定了1种新的和已知的16种木脂素。通过基于经验螺旋规则的1D / 2D NMR技术和电子圆二色性(ECD)光谱的结合,阐明了新型木脂素(7R,8S)-9-乙酰基-脱氢二癸二烯醇(1)的绝对构型。抗神经炎生物测定表明,化合物1,(7R,8S)-脱氢二松柏油醇(2),赤藓型愈创木脂甘油-β-松柏油基醚(5)和苏式-愈创甘油基甘油-β-松柏油基醚(6)表现出显着的抑制作用没有生产。其中,新木脂素1和2的活性比阳性对照(NG-单甲基-1-精氨酸,1-NMMA)强,IC50值分别为9.3和3.9μM。此外,还发现1和2均可浓度依赖性地抑制LPS刺激的BV-2细胞中TNF-α的释放。结论结果表明木脂素是“川木通”的主要成分,其抗神经炎活性强烈支持该草药在炎症中的传统应用。此外,二氢苯并[b]呋喃新木聚糖1和2以及芒草菜豆可进一步用作治疗炎症介导的神经退行性疾病和衰老相关疾病的新治疗剂。

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