A rapid screening assay for antioxidant potential of natural and synthetic agents in vitro

被引:2
作者
Srinivasan, P [1 ]
Vadhanam, MV [1 ]
Arif, JM [1 ]
Gupta, RC [1 ]
机构
[1] Univ Kentucky, Med Ctr, Dept Prevent Med & Environm Hlth, Lexington, KY 40536 USA
关键词
8-oxodG; P-32-postlabeling; ellagic acid; epigallocatechin gallate; Fenton reaction; oxidative stress;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
There are literally thousands of known agents with potential chemopreventive and antioxidant activity; however, the expanding list of natural and synthetic compounds makes it difficult to test every agent in the widely accepted 2-year animal bioassay and human clinical trials. Therefore, short-term screening assays are needed to sort out the most efficacious compounds for long-term animal studies. In the present study, the identification of chemopreventive agents with efficacious antioxidant potential was explored with a Cu2+-mediated Fenton-type reaction, coupled with oxidative DNA lesion detection by P-32-postlabeling. Several agents inhibited the fort-nation of 8-oxo-2'-deoxyguanosine (8-oxodG), a benchmark oxidative DNA lesion, but ellagic acid, a polyphenol found in berries, offered maximal (>80%) inhibition of 8-oxodG formation. However, a well-known tea polyphenol, epigallocatechin gallate, along with silymarin and D,L-sulforaphane, exhibited a pro-oxidant effect, with 50-70% increase in 8-oxodG induction. In general, our results agree with the reported antioxidant - pro-oxidant activities of the compounds, rendering, this in vitro screening assay to be useful in determining the antioxidant potential of compounds rapidly and cost-effectively.
引用
收藏
页码:983 / 986
页数:4
相关论文
共 20 条
[1]   THE EFFECT OF VARIOUS ANTIOXIDANTS AND OTHER MODIFYING AGENTS ON OXYGEN-RADICAL-GENERATED DNA-DAMAGE IN HUMAN-LYMPHOCYTES IN THE COMET ASSAY [J].
ANDERSON, D ;
YU, TW ;
PHILLIPS, BJ ;
SCHMEZER, P .
MUTATION RESEARCH, 1994, 307 (01) :261-271
[2]  
Bertram John S., 2000, Molecular Aspects of Medicine, V21, P167, DOI 10.1016/S0098-2997(00)00007-8
[3]   The prevention of lung cancer induced by a tobacco-specific carcinogen in rodents by green and black tea [J].
Chung, FL .
PROCEEDINGS OF THE SOCIETY FOR EXPERIMENTAL BIOLOGY AND MEDICINE, 1999, 220 (04) :244-248
[4]   Mechanisms of N-acetylcysteine in the prevention of DNA damage and cancer, with special reference to smoking-related end-points [J].
De Flora, S ;
Izzotti, A ;
D'Agostini, F ;
Balansky, RM .
CARCINOGENESIS, 2001, 22 (07) :999-1013
[5]   Sensitive detection of 8-hydroxy-2'-deoxyguanosine in DNA by P-32-postlabeling assay and the basal levels in rat tissues [J].
Devanaboyina, U ;
Gupta, RC .
CARCINOGENESIS, 1996, 17 (05) :917-924
[6]   Quercetin and myricetin protect against hydrogen peroxide-induced DNA damage (strand breaks and oxidised pyrimidines) in human lymphocytes [J].
Duthie, SJ ;
Collins, AR ;
Duthie, GG ;
Dodson, VL .
MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 1997, 393 (03) :223-231
[7]   FREE-RADICAL DAMAGE TO PROTEIN AND DNA - MECHANISMS INVOLVED AND RELEVANT OBSERVATIONS ON BRAIN UNDERGOING OXIDATIVE STRESS [J].
FLOYD, RA ;
CARNEY, JM .
ANNALS OF NEUROLOGY, 1992, 32 :S22-S27
[8]  
Gupta R. C., 1996, P45
[9]   An improved 32P-postlabeling assay for the sensitive detection of 8-oxodeoxyguanosine in tissue DNA [J].
Gupta, RC ;
Arif, JM .
CHEMICAL RESEARCH IN TOXICOLOGY, 2001, 14 (08) :951-957
[10]  
Gutteridge JMC, 2000, ANN NY ACAD SCI, V899, P136, DOI 10.1111/j.1749-6632.2000.tb06182.x