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黄连解毒汤及其主要成分在其血浆谱中对神经氨酸酶-1的抑制活性。

Inhibition activity of a traditional Chinese herbal formula Huang-Lian-Jie-Du-Tang and its major components found in its plasma profile on neuraminidase-1.

机构信息

Department of Pharmacy, 302 Military Hospital of China, Beijing, People's Republic of China.

China Military Institute of Chinese Medicine, 302 Military Hospital of China, Beijing, People's Republic of China.

出版信息

Sci Rep. 2017 Nov 14;7(1):15549. doi: 10.1038/s41598-017-15733-7.

DOI:10.1038/s41598-017-15733-7
PMID:29138445
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5686190/
Abstract

Huang-Lian-Jie-Du-Tang (HLJDT), a traditional formula with four TCM herbs, has been used for hundred years for different diseases. The current study aimed to assess the inhibitory activity of HLJDT against H1N1 neuraminidase (NA-1), and identify potent NA-1 inhibitors from its plasma profile. The in vitro NA-1 study has shown that the water extract of HLJDT potently inhibited NA-1 (IC = 112.6 μg/ml; Ki = 55.6 μg/ml) in a competitive mode. The IC values of the water extracts of its four herbs were as follows: Coptidis Rhizoma, 96.1 μg/ml; Phellodendri Chinensis Cortex, 108.6 μg/ml; Scutellariae Radix, 303.5 μg/ml; Gardeniae Fructus, 285.0 μg/ml. Thirteen compounds found in the plasma profile of HLJDT were also identified as potent NA-1 inhibitors, which included jatrorrhizine, palmatine, epiberberine, geniposide, oroxylin A, berberine, coptisine, baicalein, wogonoside, phellodendrine, wogonin, oroxylin A-7-O-glucuronide and baicalin (sorted in ascending order by their IC values). Their inhibitory activities were consistent with molecular docking analysis when considering crystallographic water molecules in the ligand-binding pocket of NA-1. Our current findings suggested that HLJDT can be used as a complementary medicine for H1N1 infection and its potent active compounds can be developed as NA-1 inhibitors.

摘要

黄连解毒汤(HLJDT)是一种由四味中药组成的传统方剂,百年来一直用于治疗各种疾病。本研究旨在评估 HLJDT 对 H1N1 神经氨酸酶(NA-1)的抑制活性,并从其血浆谱中鉴定出强效的 NA-1 抑制剂。体外 NA-1 研究表明,HLJDT 的水提取物以竞争性方式强烈抑制 NA-1(IC=112.6μg/ml;Ki=55.6μg/ml)。其四种草药水提取物的 IC 值如下:黄连,96.1μg/ml;黄柏,108.6μg/ml;黄芩,303.5μg/ml;栀子,285.0μg/ml。还从 HLJDT 的血浆谱中鉴定出 13 种化合物,它们也是强效的 NA-1 抑制剂,包括小檗碱、巴马汀、盐酸小檗碱、栀子苷、梓醇、黄连素、小檗碱、黄芩素、黄芩苷、黄芩苷、黄芩苷、小檗碱、梓醇-7-O-葡萄糖醛酸和黄芩苷(按其 IC 值升序排列)。当考虑到 NA-1 配体结合口袋中的结晶水分子时,它们的抑制活性与分子对接分析一致。我们的研究结果表明,HLJDT 可作为 H1N1 感染的辅助药物,其有效活性化合物可开发为 NA-1 抑制剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9f2/5686190/0e53860ef4e3/41598_2017_15733_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9f2/5686190/684b0b1c03b9/41598_2017_15733_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9f2/5686190/22b4144d1204/41598_2017_15733_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9f2/5686190/b1b164c3d5af/41598_2017_15733_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9f2/5686190/0e53860ef4e3/41598_2017_15733_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9f2/5686190/684b0b1c03b9/41598_2017_15733_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9f2/5686190/22b4144d1204/41598_2017_15733_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9f2/5686190/b1b164c3d5af/41598_2017_15733_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9f2/5686190/0e53860ef4e3/41598_2017_15733_Fig4_HTML.jpg

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