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比较 L. 和 L. 的酚类化合物组成和抗氧化潜力

Comparison of the Phenolic Compound Profile and Antioxidant Potential of L. and L.

机构信息

WALA Heilmittel GmbH, Department of Analytical Development & Research, Section Phytochemical Research, 73087 Bad Boll, Germany.

Institute of Botany, Hohenheim University, 70599 Stuttgart, Germany.

出版信息

Molecules. 2021 Mar 11;26(6):1530. doi: 10.3390/molecules26061530.

Abstract

In the present study, L. and L. were compared for the first time with regard to their phenolic compound profile and antioxidant activity by applying the 2,2-diphenyl-picryl hydrazyl radical assay. For this purpose, aerial plant parts were consecutively extracted with solvents of increasing polarity (dichloromethane, -butanol, ethyl acetate), revealing that the ethyl acetate fraction showed the highest antioxidant activity with an IC value of 12.2 ± 0.29 µg/mL compared to 17.0 ± 0.26 µg/mL for . Both species revealed the presence of luteolin, apigenin, centaureidin, and nevadensin exclusively in this most polar fraction, which are known as effective 2,2-diphenyl-picryl hydrazyl radical scavengers. The antioxidant capacity of the aforementioned fractions strikingly correlated with their total phenolic contents, which was highest in the ethyl acetate fraction of . Characterization of the metabolite profiles of both species showed only marginal differences in the presence of key compounds, whereas the concentrations of individual compounds appeared to be species-specific. Our results suggest that , based on its compound pattern and bioactivity characteristics, has similar qualities for phytotherapy as .

摘要

在本研究中,首次比较了 L.和 L.的酚类化合物谱和抗氧化活性,方法是应用 2,2-二苯基-1-苦基肼自由基测定法。为此,连续用极性递增的溶剂(二氯甲烷、正丁醇、乙酸乙酯)提取地上植物部分,结果表明,与 相比,乙酸乙酯部分具有最高的抗氧化活性,IC 值为 12.2±0.29 µg/mL,而 为 17.0±0.26 µg/mL。两种植物均仅在这一最极性的部分中存在木樨草素、芹菜素、山奈酚和新戊烯素,这些物质是已知的有效 2,2-二苯基-1-苦基肼自由基清除剂。上述部分的抗氧化能力与总酚含量显著相关,而 乙酸乙酯部分的总酚含量最高。两种植物代谢物图谱的特征表明,关键化合物的存在仅有微小差异,而个别化合物的浓度似乎是种特异性的。我们的结果表明,根据其化合物模式和生物活性特征,L.在植物疗法方面与 L.具有相似的品质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a63/8000477/1ff8e99c02a3/molecules-26-01530-g001.jpg

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