Large-scale isolation and antitumor mechanism evaluation of compounds from the traditional Chinese medicine Cordyceps Militaris

被引:16
作者
Chen, Yujiao [1 ,2 ,6 ]
Wu, Yuqian [2 ]
Li, Shouliang [2 ]
Du, Simiao [2 ]
Hao, Xuemin [3 ]
Zhang, Jian [4 ]
Gu, Pengai [5 ]
Sun, Jiachen [5 ]
Jiang, Lei [5 ]
Gai, Qijin [5 ]
Liu, Xiaomin [5 ,6 ]
Nie, Kaimei [2 ]
Zhong, Li [1 ]
Wang, Guixue [1 ]
Cao, Jun [2 ]
机构
[1] Chongqing Univ, Key Lab Biorheol Sci & Technol, State & Local Joint Engn Lab Vasc Implants, Minist Educ,Bioengn Coll, Chongqing 400030, Peoples R China
[2] Guizhou Guian Acad Precis Med Co Ltd, Guian 561113, Peoples R China
[3] Zheng YuanTang Tianjin Biotechnol Co Ltd, Tianjin 300457, Peoples R China
[4] Tianjin YaoYu Biotechnol Co Ltd, Tianjin 300457, Peoples R China
[5] Duker Tianjin Pharmaceut Technol Co Ltd, Tianjin 300457, Peoples R China
[6] Zheng YuanTang Tianjin Binhai New Area Biotechnol, Tianjin 300457, Peoples R China
关键词
C; militaris; Large-scale extraction; Ergosterol; N6-(2-hydroxyethyl) adenosine; Structure; Anti-tumor function; Anti-insomnia function; Molecular interaction; Metabolism pathways;
D O I
10.1016/j.ejmech.2020.113142
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
We established a large-scale separation and purification platform to obtain kilogram amounts of natural compounds from the extraction of the fruiting bodies of C. militaris. Seven monomeric compounds, N6-(2-hydroxyethyl) adenosine (HEA), ergosterol (E), ergosta-7,22-diene-3,5,6-triol (EI), 5 alpha,8 alpha-epidioxy(22E,24R)-ergosta-6,22-dien-3 beta-ol (ED),ergosta-7,22-dien-3 beta,5 alpha-dihydroxy-6-one (EO), (20S,22E,24R)-Eegosta-7,22-dien-3 beta,5 alpha,6 beta,9 alpha-tetraol (ET), and (24S)-5,22-stigmastadien-3 beta-ol (SE), were harvested using different solvents, and the structure of each compound was identified. The activities and functions of the isolated compounds were tested by label-free, real-time cell analysis methods at the cellular level, and their antitumor effects were verified using mouse models of Lewis and H22 tumors. The anti-insomnia effect of HEA was tested in an anti-insomnia mouse model. The interactions between E and 8 A549 cell proteins were determined. The biosynthetic pathways of HEA and E, which possess pharmacologically active monomers, were determined. This platform can provide a theoretical basis for the further development and discovery of novel natural medicines. (C) 2021 Elsevier Masson SAS. All rights reserved.
引用
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页数:12
相关论文
共 27 条
[1]   Ergosterol biosynthesis in Aspergillus fumigatus: its relevance as an antifungal target and role in antifungal drug resistance [J].
Alcazar-Fuoli, Laura ;
Mellado, Emilia .
FRONTIERS IN MICROBIOLOGY, 2013, 3
[2]   Cloning and characterization of ERG25, the Saccharomyces cerevisiae gene encoding C-4 sterol methyl oxidase [J].
Bard, M ;
Bruner, DA ;
Pierson, CA ;
Lees, ND ;
Biermann, B ;
Frye, L ;
Koegel, C ;
Barbuch, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (01) :186-190
[3]   DUALITY OF PATHWAYS IN OXIDATION OF ERGOSTEROL TO ITS PEROXIDE INVIVO [J].
BATES, ML ;
REID, WW ;
WHITE, JD .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1976, (02) :44-45
[4]   BIOSYNTHESIS OF STIGMASTEROL IN TOMATO FRUITS [J].
BENNETT, RD ;
BONNER, J ;
HEFTMANN, E ;
PURCELL, AE .
SCIENCE, 1961, 134 (348) :671-&
[5]  
[陈玉皎 Chen Yujiao], 2015, [中国新药杂志, Chinese Journal New Drugs], V24, P813
[6]   MOLECULAR-CLONING, CHARACTERIZATION, AND OVEREXPRESSION OF ERG7 THE SACCHAROMYCES-CEREVISIAE GENE ENCODING LANOSTEROL SYNTHASE [J].
COREY, EJ ;
MATSUDA, SPT ;
BARTEL, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (06) :2211-2215
[7]   CORDYCEPIN, A METABOLIC PRODUCT ISOLATED FROM CULTURES OF CORDYCEPS-MILITARIS (LINN) LINK [J].
CUNNINGHAM, KG ;
MANSON, W ;
SPRING, FS ;
HUTCHINSON, SA .
NATURE, 1950, 166 (4231) :949-949
[8]   Biosynthesis of β-sitosterol and stigmasterol in Croton sublyratus proceeds via a mixed origin of isoprene units [J].
De-Eknamkul, W ;
Potduang, B .
PHYTOCHEMISTRY, 2003, 62 (03) :389-398
[9]   ERGOSTEROL BIOSYNTHESIS: A FUNGAL PATHWAY FOR LIFE ON LAND? [J].
Dupont, Sebastien ;
Lemetais, Guillaume ;
Ferreira, Thierry ;
Cayot, Philippe ;
Gervais, Patrick ;
Beney, Laurent .
EVOLUTION, 2012, 66 (09) :2961-2968
[10]   BIOSYNTHESIS OF ERGOSTEROL IN YEAST - EVIDENCE FOR MULTIPLE PATHWAYS [J].
FRYBERG, M ;
UNRAU, AM ;
OEHLSCHLAGER, AC .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1973, 95 (17) :5747-5757