A glutathione S-transferase inducer from papaya, rapid screening, identification and structure-activity relationship of isothiocyanates

被引:39
作者
Nakamura, Y [1 ]
Morimitsu, Y
Uzu, T
Ohigashi, H
Murakami, A
Naito, Y
Nakagawa, Y
Osawa, T
Uchida, K
机构
[1] Kyoto Univ, Grad Sch Agr, Div Appl Life Sci, Kyoto 6068502, Japan
[2] Nagoya Univ, Grad Sch Bioagr Sci, Lab Food & Biodynam, Nagoya, Aichi 4648601, Japan
[3] Kinki Univ, Fac Biol Oriented Sci & Technol, Dept Biotechnol Sci, Wakayama 6496493, Japan
基金
日本学术振兴会;
关键词
isothiocyanate; glutathione S-transferase; fruit; papaya; rat normal liver epithelial cell line;
D O I
10.1016/S0304-3835(00)00487-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We have developed a simple system for rapid detection and measurement of glutathione S-transferase placental form (GSTP1) that detoxify polycyclic aromatic hydrocarbons using the cultured rat normal liver epithelial cell line, (RL34) cells. Survey of fruit extracts for GST inducing ability identified both papaya and avocado as significant sources. Benzyl isothiocyanate (BITC) was isolated from papaya methanol extract as a principal inducer of GST activity. Further, the GST inducing ability of a total of 20 isothiocyanates (ITCs) and their derivatives was investigated. Some ITCs showed significant induction, and BITC was one of the most potent inducers among all compounds tested in the present study. The modification of isothiocyanate group (-NCS) or introduction of substituent group to the a-carbon modifies GST induction. Moreover, a significant correlation (P < 0.01, r = 0.913) between the GST activity enrichment and GSTP1 protein induction by ITCs was observed. We also indicated that phenethyl ITC and nitrophenyl ITC, potently inducing GST activity, but not inactive benzyl isocyanate, are potential inducers of intracellular reactive oxygen intermediates (ROIs). Our system of GSTP1 induction is appropriate for the chemical research such as screening and identification of novel type of inducers as well as the structure-activity relationship studies, providing mechanistic insight into essential structural elements for GSTP1 induction. (C) 2000 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:193 / 200
页数:8
相关论文
共 36 条
[11]  
2-2
[12]  
HOSHIKA T, 1978, Okayama Igakkai Zasshi, V90, P1377
[13]  
HUANG MT, 1994, ACS SYM SER, V546, P2
[14]   An improved procedure for the preparation of isothiocyanates from primary amines by using hydrogen peroxide as the dehydrosulfurization reagent [J].
Li, G ;
Tajima, H ;
Ohtani, T .
JOURNAL OF ORGANIC CHEMISTRY, 1997, 62 (13) :4539-4540
[15]   Mechanism of action of dietary chemoprotective agents in rat liver: induction of phase I and II drug metabolizing enzymes and aflatoxin B-1 metabolism [J].
Manson, MM ;
Ball, HWL ;
Barrett, MC ;
Clark, HL ;
Judah, DJ ;
Williamson, G ;
Neal, GE .
CARCINOGENESIS, 1997, 18 (09) :1729-1738
[16]  
MEDESTO RR, 1973, BIOCHIM BIOPHYS ACTA, V295, P283
[17]   Niaziminin, a thiocarbamate from the leaves of Moringa oleifera, holds a strict structural requirement for inhibition of tumor-promoter-induced Epstein-Barr virus activation [J].
Murakami, A ;
Kitazono, Y ;
Jiwajinda, S ;
Koshimizu, K ;
Ohigashi, H .
PLANTA MEDICA, 1998, 64 (04) :319-323
[18]   Inhibition of early-phase exogenous and endogenous liver carcinogenesis in transgenic rats harboring a rat glutathione S-transferase placental form gene [J].
Nakae, D ;
Denda, A ;
Kobayashi, Y ;
Akai, H ;
Kishida, H ;
Tsujiuchi, T ;
Konishi, Y ;
Suzuki, T ;
Muramatsu, M .
JAPANESE JOURNAL OF CANCER RESEARCH, 1998, 89 (11) :1118-1125
[19]  
Nakamura Y, 2000, CANCER RES, V60, P219
[20]  
Ogawa K, 1998, INT J CANCER, V76, P851