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利用网络药理学研究不同提取方法的蓝刺头(Boiss. & Noë)Grierson 化学成分谱和生物学活性的组合。

Combining chemical profiles and biological abilities of different extracts from Tanacetum nitens (Boiss. & Noë) Grierson using network pharmacology.

机构信息

Department of Pharmaceutical and Pharmacological Sciences, University of Padova, Padova, Italy.

Department of Botany, Faculty of Science, University of Khartoum, Khartoum, Sudan.

出版信息

Arch Pharm (Weinheim). 2024 Sep;357(9):e2400194. doi: 10.1002/ardp.202400194. Epub 2024 Jun 14.

Abstract

Tanacetum nitens (Boiss. & Noë) Grierson is an aromatic perennial herb used in Turkish traditional medicine to treat headache, fever, and skin diseases. This study aimed to investigate the chemical composition, antioxidant, enzyme inhibition, and cytotoxic properties of T. nitens aerial parts. Organic solvent extracts were prepared by sequential maceration in hexane, dichloromethane, ethyl acetate, and methanol while aqueous extracts were obtained by maceration or infusion. Nuclear magnetic resonance (NMR) and LC-DAD-MS analysis allowed the identification and quantification of different phytoconstituents including parthenolide, tanacetol B, tatridin B, quinic acid derivatives, β-sitosterol, and glycoside derivatives of quercetin and luteolin. The type and amount of these phytochemicals recovered by each solvent were variable and significant enough to impact the biological activities of the plant. Methanolic and aqueous extracts displayed the highest scavenging and ions-reducing properties while the dichloromethane and ethyl acetate extracts exerted the best total antioxidant activity and metal chelating power. Results of enzyme inhibition activity showed that the hexane, ethyl acetate, and dichloromethane extracts had comparable anti-acetylcholinesterase activity and the latter extract revealed the highest anti-butyrylcholinesterase activity. The best α-amylase and α-glucosidase inhibition activities were obtained from the hexane extract. The dichloromethane and ethyl acetate extracts exhibited the highest cytotoxic effect against the prostate carcinoma DU-145 cells. In conclusion, these findings indicated that T. nitens can be a promising source of biomolecules with potential therapeutic applications.

摘要

金光菊(Boiss. & Noë)格里尔是一种芳香的多年生草本植物,在土耳其传统医学中用于治疗头痛、发烧和皮肤病。本研究旨在研究金光菊地上部分的化学成分、抗氧化、酶抑制和细胞毒性特性。通过连续用正己烷、二氯甲烷、乙酸乙酯和甲醇浸提制备有机溶剂提取物,而水提取物则通过浸提或浸渍获得。核磁共振(NMR)和 LC-DAD-MS 分析允许鉴定和定量不同的植物成分,包括角蒿内酯、tanacetol B、tatridin B、奎尼酸衍生物、β-谷甾醇和槲皮素和木犀草素的糖苷衍生物。每种溶剂回收的这些植物化学成分的类型和数量是可变的,足以影响植物的生物活性。甲醇和水提取物显示出最高的清除和离子还原特性,而二氯甲烷和乙酸乙酯提取物表现出最高的总抗氧化活性和金属螯合能力。酶抑制活性的结果表明,正己烷、乙酸乙酯和二氯甲烷提取物具有相当的乙酰胆碱酯酶抑制活性,而后者提取物表现出最高的丁酰胆碱酯酶抑制活性。正己烷提取物对α-淀粉酶和α-葡萄糖苷酶的抑制活性最高。二氯甲烷和乙酸乙酯提取物对前列腺癌 DU-145 细胞表现出最高的细胞毒性作用。总之,这些发现表明,金光菊可能是具有潜在治疗应用的生物分子的有前途的来源。

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