Comparative effects of eight varieties of blackberry on mutagenesis

被引:18
作者
Tate, P
Kuzmar, A
Smith, SW
Wedge, DE
Larcom, LL [1 ]
机构
[1] Clemson Univ, Dept Biol Sci, Clemson, SC 29634 USA
[2] Clemson Univ, Dept Phys & Astron, Clemson, SC 29634 USA
[3] Greenville Mem Hosp Syst, Greenville, SC 29605 USA
[4] Univ Mississippi, USDA ARS, Nat Prod Utilizat Res Unit, University, MS 38677 USA
[5] Univ Mississippi, Thad Cochran Natl Ctr Nat Prod Res, University, MS 38677 USA
关键词
mutagenesis inhibition; berries; Ames assay; blackberry varieties;
D O I
10.1016/S0271-5317(03)00083-6
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Diets containing large amounts of fruits and vegetables are known to decrease the probability of developing cancer. The chemical composition of fruits can vary with their genetic characteristics and the environmental conditions under which they are cultivated. Because of this variability, different varieties of the same fruit could be expected to have different effects on processes leading to carcinogenesis. Blackberries have been shown to have anti-carcinogenic potential. Since somatic mutations play a major role in the initiation and progression of cancer, we have compared eight varieties of blackberry grown under the same conditions for their abilities to inhibit carcinogen-induced mutagenesis. Using the Ames assay, we have measured the effects of each of the eight varieties on: 1) mutation induction by 2-amino anthracene (2AA), 2) mutation induction by methyl methanesulfonate (MMS) and 3) cell survival. All varieties were found to strongly suppress 2AA mutagenesis, but have minimal effect on MMS mutagenesis. Experiments were performed with berry juice and with homogenized berries. In addition, berries extracts were acidified to-simulate changes which might be caused by the digestive process. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:971 / 979
页数:9
相关论文
共 19 条
[11]   REVISED METHODS FOR THE SALMONELLA MUTAGENICITY TEST [J].
MARON, DM ;
AMES, BN .
MUTATION RESEARCH, 1983, 113 (3-4) :173-215
[12]   DETECTION OF CARCINOGENS AS MUTAGENS IN SALMONELLA MICROSOME TEST - ASSAY OF 300 CHEMICALS [J].
MCCANN, J ;
CHOI, E ;
YAMASAKI, E ;
AMES, BN .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1975, 72 (12) :5135-5139
[13]   Metabolic activation of heterocyclic amines and other procarcinogens in Salmonella typhimurium umu tester strains expressing human cytochrome P4501A1, 1A2, 1B1, 2C9, 2D6, 2E1, and 3A4 and human NADPH-P450 reductase and bacterial O-acetyltransferase [J].
Oda, Y ;
Aryal, P ;
Terashita, T ;
Gillam, EMJ ;
Guengerich, FP ;
Shimada, T .
MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 2001, 492 (1-2) :81-90
[14]  
Pieper RO, 1998, CONT CANC RES, P33
[15]  
ROMEO JT, 1999, RECENT ADV PHYTOCHEM, P432
[16]   Inhibition of metabolic activation of the promutagens, benzo[a]pyrene, 2-aminofluorene and 2-aminoanthracene by furanochromones in Salmonella typhimurium [J].
Schimmer, O ;
Rauch, P .
MUTAGENESIS, 1998, 13 (04) :385-389
[17]   Phenolic compounds and antioxidant capacity of Georgia-grown blueberries and blackberries [J].
Sellappan, S ;
Akoh, CC ;
Krewer, G .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2002, 50 (08) :2432-2438
[18]  
STONER GD, 1995, J CELL BIOCHEM, P169
[19]   INHIBITORY EFFECT OF ELLAGIC ACID ON N-2-FLUORENYLACETAMIDE-INDUCED LIVER CARCINOGENESIS IN MALE ACI/N RATS [J].
TANAKA, T ;
IWATA, H ;
NIWA, K ;
MORI, Y ;
MORI, H .
JAPANESE JOURNAL OF CANCER RESEARCH, 1988, 79 (12) :1297-1303