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对L.(艾菊)代谢物谱和生物学潜力的深入研究。

An In-Depth Study of Metabolite Profile and Biological Potential of L. (Costmary).

作者信息

Gevrenova Reneta, Zengin Gokhan, Sinan Kouadio Ibrahime, Zheleva-Dimitrova Dimitrina, Balabanova Vessela, Kolmayer Maxime, Voynikov Yulian, Joubert Olivier

机构信息

Department of Pharmacognosy, Faculty of Pharmacy, Medical University-Sofia, 1431 Sofia, Bulgaria.

Department of Biology, Faculty of Science, Selcuk University, Konya 42250, Turkey.

出版信息

Plants (Basel). 2022 Dec 20;12(1):22. doi: 10.3390/plants12010022.

Abstract

Asteraceae species Tanacetum balsamita L. (costmary) is renowned for its traditional usage as an aromatic, carminative and tonic plant. This work aimed at in-depth study of the phytochemical and in vitro biological profilings of methanol−aqueous extracts from the costmary leaves, flower heads and roots. An UHPLC-HRMS analysis revealed more than 100 secondary metabolites including 24 acylquinic acids, 43 flavonoid glycosides, aglycones and methoxylated derivatives together with 15 phenolic acids glycosides. For the first time, 91 compounds are reported in the costmary. The flower heads extract possessing the highest content of total phenolics and flavonoids, actively scavenged DPPH (84.54 ± 3.35 mgTE/g) and ABTS radicals (96.35 ± 2.22 mgTE/g), and showed the highest reducing potential (151.20 and 93.22 mg TE/g for CUPRAC and FRAP, respectively). The leaves extract exhibited the highest inhibition towards acetyl- and butyrylcholinesterase (2.11 and 2.43 mg GALAE/g, respectively) and tyrosinase (54.65 mg KAE/g). The root extract inhibited α-glucosidase (0.71 ± 0.07 mmol ACAE/g), α-amylase (0.43 ± 0.02 mmol ACAE/g) and lipase (8.15 ± 1.00 mg OE/g). At a concentration >2 µg/mL, a significant dose dependent reduction of cell viability towards THP-1 monocyte leukemic cells was observed. Costmary could be recommended for raw material production with antioxidant and enzyme inhibitory properties.

摘要

菊科植物香艾菊(Tanacetum balsamita L.)作为一种芳香、驱风健胃和滋补的植物,其传统用途广为人知。这项研究旨在深入探究香艾菊叶片、花头和根部的甲醇-水提取物的植物化学成分及体外生物学特性。超高效液相色谱-高分辨质谱分析揭示了100多种次生代谢产物,包括24种酰基奎宁酸、43种黄酮苷、苷元及甲氧基化衍生物,还有15种酚酸苷。首次在香艾菊中报道了91种化合物。花头提取物的总酚和黄酮含量最高,能有效清除DPPH自由基(84.54 ± 3.35 mgTE/g)和ABTS自由基(96.35 ± 2.22 mgTE/g),并表现出最高的还原能力(CUPRAC和FRAP分别为151.20和93.22 mg TE/g)。叶片提取物对乙酰胆碱酯酶和丁酰胆碱酯酶(分别为2.11和2.43 mg GALAE/g)以及酪氨酸酶(54.65 mg KAE/g)的抑制作用最强。根部提取物能抑制α-葡萄糖苷酶(0.71 ± 0.07 mmol ACAE/g)、α-淀粉酶(0.43 ± 0.02 mmol ACAE/g)和脂肪酶(8.15 ± 1.00 mg OE/g)。在浓度>2 µg/mL时,观察到对THP-1单核细胞白血病细胞的细胞活力有显著的剂量依赖性降低。香艾菊因其具有抗氧化和酶抑制特性,可推荐用于原料生产。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a540/9824382/a281136d40a1/plants-12-00022-g001.jpg

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