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朝鲜罂粟蜂花粉中有助于体外抗流感活性的神经氨酸酶抑制剂的特性分析

Characterization of Neuraminidase Inhibitors in Korean Papaver rhoeas Bee Pollen Contributing to Anti-Influenza Activities In Vitro.

作者信息

Lee In-Kyoung, Hwang Byung Soon, Kim Dae-Won, Kim Ji-Yul, Woo E-Eum, Lee Yoon-Ju, Choi Hwa Jung, Yun Bong-Sik

机构信息

Division of Biotechnology and Advanced Institute of Environment and Bioscience, Chonbuk National University, Iksan-si, Republic of Korea.

Department of Beauty Science, Kwangju Women's University, Sanjeong-dong, Gwangsan-gu, Kwangju, Republic of Korea.

出版信息

Planta Med. 2016 Apr;82(6):524-9. doi: 10.1055/s-0041-111631. Epub 2016 Feb 5.

DOI:10.1055/s-0041-111631
PMID:26848705
Abstract

The active constituents of Korean Papaver rhoeas bee pollen conferring neuraminidase inhibitory activities (H1N1, H3N2, and H5N1) were investigated. Six flavonoids and one alkaloid were isolated and characterized by nuclear magnetic resonance and mass spectrometry data. These included kaempferol-3-sophoroside (1), kaempferol-3-neohesperidoside (2), kaempferol-3-sambubioside (3), kaempferol-3-glucoside (4), quercetin-3-sophoroside (5), luteolin (6), and chelianthifoline (7). All compounds showed neuraminidase inhibitory activities with IC50 values ranging from 10.7 to 151.1 µM. The most potent neuraminidase inhibitor was luteolin, which was the dominant content in the ethyl acetate fraction. All tested compounds displayed noncompetitive inhibition of H3N2 neuraminidase. Furthermore, compounds 1-7 all reduced the severity of virally induced cytopathic effects as determined by the Madin-Darby canine kidney cell-based assay showing antiviral activity with IC50 values ranging from 10.7 to 33.4 µM (zanamivir: 58.3 µM). The active compounds were quantified by high-performance liquid chromatography, and the total amount of compounds 1-7 made up about 0.592 g/100 g bee pollen, contributing a rich resource of a natural antiviral product.

摘要

研究了朝鲜罂粟蜂花粉中具有神经氨酸酶抑制活性(针对H1N1、H3N2和H5N1)的活性成分。通过核磁共振和质谱数据分离并鉴定了六种黄酮类化合物和一种生物碱。这些化合物包括山奈酚-3-槐糖苷(1)、山奈酚-3-新橙皮糖苷(2)、山奈酚-3-接骨木二糖苷(3)、山奈酚-3-葡萄糖苷(4)、槲皮素-3-槐糖苷(5)、木犀草素(6)和白屈菜红碱(7)。所有化合物均表现出神经氨酸酶抑制活性,IC50值在10.7至151.1μM之间。最有效的神经氨酸酶抑制剂是木犀草素,它是乙酸乙酯馏分中的主要成分。所有测试化合物对H3N2神经氨酸酶均表现出非竞争性抑制作用。此外,通过基于Madin-Darby犬肾细胞的试验测定,化合物1-7均降低了病毒诱导的细胞病变效应的严重程度,显示出抗病毒活性,IC50值在10.7至33.4μM之间(扎那米韦:58.3μM)。通过高效液相色谱法对活性化合物进行了定量,化合物1-7的总量约为0.592 g/100 g蜂花粉,为天然抗病毒产品提供了丰富的资源。

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