The constituents of Cibotium barometz and their permeability in the human Caco-2 monolayer cell model

被引:46
作者
Wu, Qi [1 ]
Yang, Xiu-Wei [1 ]
机构
[1] Peking Univ, State Key Lab Nat & Biomimet Drugs, Dept Nat Med, Sch Pharmaceut Sci, Beijing 100191, Peoples R China
基金
国家高技术研究发展计划(863计划);
关键词
Cibotium barometz; Dicksoniaceae; Rhizome; Caco-2 cell monolayer model; Human intestinal permeation; EFFLUX;
D O I
10.1016/j.jep.2009.07.017
中图分类号
Q94 [植物学];
学科分类号
071001 [植物学];
摘要
Ethnopharmacological relevance: Cibotium barometz(L)J. Sm. (Dicksoniaceae) has been traditionally used as anti-inflammatory and anodyne. Aim of the study: To investigate the constituents in the rhizomes of Cibotium barometz, and evaluate their permeability in the human Caco-2 model. Materials and methods: The rhizomes extracts of Cibotium, barometz were isolated by chromatographic techniques. Structures of isolated compounds were identified by spectroscopic methods. The permeability of the main constituents was evaluated using human Caco-2 cell monolayer as a model system. Results: Three unusual sesquiterpenes having 1-indanone nucleus (1, 3 and 4) and an unusual orthoester spiropyranosyl derivative of protocatechuic acid (2) were isolated from the rhizomes of Cibotium barometz. Among these, the bilateral permeation of 1, 3 and 4 in Caco-2 model was examined. The apparent permeability coefficients (P-app) of 1 was identical with those of propranolol, which is often used as reference standard of high permeability. The P pp values of 3 and 4 were in agreement with those of atenolol, which is often used as reference standard of poor permeability. The permeation rates of 1, 3 and 4 increased linearly as a function of time up to 180 min and with the concentration within the test range of 25-200 mu M. Conclusions: This is the first report on the presence of compounds 2 and 3 in this plant and 4 was a new compound. Compound 1 is assigned for a well-absorbed, and 2 and 3 are assigned for the poorly absorbed compounds in human intestine. A passive diffusion mechanism for transport of 1, 3 and 4 in Caco-2 model was proposed. The results provided some useful information for predicting the oral bioavailability of 1, 3 and 4. (C) 2009 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:417 / 422
页数:6
相关论文
共 16 条
[1]
Cheng QH, 2003, PROGR PHARM SCI, V27, P298
[2]
GAO J, 2000, CURRENT PROTOCOLS PH
[3]
STUDIES ON THE TAIWAN FOLK MEDICINE .3. A SMOOTH-MUSCLE RELAXANT FROM ONYCHIUM-SILICULOSUM, ONITIN [J].
HO, ST ;
YANG, MS ;
WU, TS ;
WANG, CH .
PLANTA MEDICA, 1985, 51 (02) :148-150
[4]
Hepatoprotective and free radical scavenging activities of phenolic petrosins and flavonoids isolated from Equisetum arvense [J].
Oh, H ;
Kim, DH ;
Cho, JH ;
Kim, YC .
JOURNAL OF ETHNOPHARMACOLOGY, 2004, 95 (2-3) :421-424
[5]
Cyathenosin A, a spiropyranosyl derivative of protocatechuic acid from Cyathea phalerata [J].
Pizzolatti, Moacir Geraldo ;
Brighente, Ines Maria Costa ;
Bortoluzzi, Adailton Joao ;
Schripsema, Jan ;
Verdi, Luiz Gonzaga .
PHYTOCHEMISTRY, 2007, 68 (09) :1327-1330
[6]
SATAKE T, 1984, CHEM PHARM BULL, V32, P4620
[7]
Smooth muscle relaxant activity of pterosin Z and related compounds [J].
Sheridan, H ;
Frankish, N ;
Farrell, R .
PLANTA MEDICA, 1999, 65 (03) :271-272
[8]
In vitro leishmanicidal activity of some scarce natural products [J].
Takahashi, M ;
Fuchino, H ;
Sekita, S ;
Satake, M .
PHYTOTHERAPY RESEARCH, 2004, 18 (07) :573-578
[9]
The efflux of flavonoids morin, isorhamnetin-3-O-rutinoside and diosmetin-7-O-β-D-xylopyranosyl-(1-6)-β-D-glucopyranoside in the human intestinal cell line Caco-2 [J].
Tian, Xiaojuan ;
Yang, Xiaoda ;
Wang, Kui ;
Yang, Xiuwei .
PHARMACEUTICAL RESEARCH, 2006, 23 (08) :1721-1728
[10]
[吴琦 WU Qi], 2007, [天然产物研究与开发, Natural Product R & D], V19, P240