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首页> 外文期刊>Molecules >Flavonoids, Antioxidant Potential, and Acetylcholinesterase Inhibition Activity of the Extracts from the Gametophyte and Archegoniophore of Marchantia polymorpha L.
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Flavonoids, Antioxidant Potential, and Acetylcholinesterase Inhibition Activity of the Extracts from the Gametophyte and Archegoniophore of Marchantia polymorpha L.

机译:多形Marcantia L.的配子体和弓形虫提取物的类黄酮,抗氧化潜力和乙酰胆碱酯酶抑制活性。

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摘要

Marchantia polymorpha L. is a representative bryophyte used as a traditional Chinese medicinal herb for scald and pneumonia. The phytochemicals in M. polymorpha L. are terpenoids and flavonoids, among which especially the flavonoids show significant human health benefits. Many researches on the gametophyte of M. polymorpha L . have been reported. However, as the reproductive organ of M. polymorpha L . , the bioactivity and flavonoids profile of the archegoniophore have not been reported, so in this work the flavonoid profiles, antioxidant and acetylcholinesterase inhibition activities of the extracts from the archegoniophore and gametophyte of M. polymorpha L . were compared by radical scavenging assay methods (DPPH, ABTS, O 2? ), reducing power assay, acetylcholinesterase inhibition assay and LC-MS analysis. The results showed that the total flavonoids content in the archegoniophore was about 10-time higher than that of the gametophyte. Differences between the archegoniophore and gametophyte of M. polymorpha L. were observed by LC-MS analysis. The archegoniophore extracts showed stronger bio-activities than those of the gametophyte. The archegoniophore extract showed a significant acetylcholinesterase inhibition, while the gametophyte extract hardly inhibited it.
机译:多形花(Marcantia polymorpha L.)是代表性的苔藓植物,用作烫伤和肺炎的传统中草药。多形麦芽孢杆菌中的植物化学物质是萜类和黄酮类,其中尤其是类黄酮对人类健康具有显着的益处。关于多形支原体配子体的许多研究。已经报道。但是,作为多形分支杆菌的生殖器官。 ,没有报道过弓手虫的生物活性和类黄酮谱,因此在这项工作中,多形支原体弓手虫和配子体提取物的类黄酮谱,抗氧化剂和乙酰胆碱酯酶抑制活性。用自由基清除测定法(DPPH,ABTS,O 2′),还原能力测定,乙酰胆碱酯酶抑制测定和LC-MS分析比较。结果表明,始祖鸟的总黄酮含量比配子体高约10倍。通过LC-MS分析观察到了多形支原体的古菌和配子体之间的差异。始祖植物提取物显示出比配子体更强的生物活性。弓形虫提取物显示出显着的乙酰胆碱酯酶抑制作用,而配子体提取物几乎没有抑制它。

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