Pharmacokinetic study of allixin, a phytoalexin produced by garlic

被引:12
作者
Kodera, Y
Ichikawa, M
Yoshida, J
Kashimoto, N
Uda, N
Sumioka, I
Ide, N
Ono, K
机构
[1] Wakunaga Pharmaceut Co Ltd, Healthcare Inst, Hiroshima 7391195, Japan
[2] Hiroshima Univ, Grad Sch Adv Sci Matter, Dept Mol Biotechnol, Hiroshima 7398526, Japan
关键词
allixin; pharmacokinetic; metabolism; inclusion compound; phytoalexin;
D O I
10.1248/cpb.50.354
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The pharmacokinetic behavior of allixin (3-hydroxy-5-methoxy-6-methyl-2-penthyl-4H-pyran-4-one) was investigated in an experimental animal, mice. Allixin was administered using an inclusion compound because the solubility of allixin in aqueous solution is very low. The allixin content in serum and in the organs of administered animals was analyzed by liquid chromatography (LC)-MS. Most of the administered allixin disappeared within 2 h, and the bioavailability of allixin was estimated to be 31% by obtained area under the blood concentration-time curve (AITC). The metabolites of allixin were studied using the metabolic enzyme fraction of liver and liver homogenate. Several new peaks corresponding to allixin metabolites were observed in the HPLC chromatoprofile. The chemical structure of the metabolites was investigated using LC-MS and NMR. Three of them were identified as allixin metabolites having a hydroxylated pentyl group.
引用
收藏
页码:354 / 363
页数:10
相关论文
共 34 条
[1]  
Bailey J. A., 1982, PHYTOALEXINS
[2]   EFFECTS OF THE PYRONES, MALTOL AND ETHYL MALTOL, ON IRON-ABSORPTION FROM THE RAT SMALL-INTESTINE [J].
BARRAND, MA ;
CALLINGHAM, BA ;
HIDER, RC .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1987, 39 (03) :203-211
[3]   Improvement of the in vitro dissolution of praziquantel by complexation with α-, β- and γ-cyclodextrins [J].
Becket, G ;
Schep, LJ ;
Tan, MY .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1999, 179 (01) :65-71
[4]   Plant-fungal interactions: the search for phytoalexins and other antifungal compounds from higher plants [J].
Grayer, RJ ;
Kokubun, T .
PHYTOCHEMISTRY, 2001, 56 (03) :253-263
[5]  
GUO Z, 1990, Planta Medica, V56, P692, DOI 10.1055/s-2006-961372
[6]   Chemopreventive effect of S-allylcysteine and its relationship to the detoxification enzyme glutathione S-transferase [J].
Hatono, S ;
Jimenez, A ;
Wargovich, MJ .
CARCINOGENESIS, 1996, 17 (05) :1041-1044
[7]  
Hirao Y., 1987, PHYTOTHER RES, V1, P161, DOI [10.1002/ptr.2650010406, DOI 10.1002/PTR.2650010406]
[8]   S-allylcysteine attenuates oxidative stress in endothelial cells [J].
Ide, N ;
Lau, BHS .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1999, 25 (05) :619-624
[9]  
IKEDA K, 1975, CHEM PHARM BULL, V23, P201
[10]  
IKEDA K, 1973, YAKKYOKU, V24, P53