Genotoxicity studies on licorice flavonoid oil (LFO)

被引:25
作者
Nakagawa, K. [2 ]
Hidaka, T. [2 ]
Kitano, M. [1 ]
Asakura, M. [3 ]
Kamigaito, T. [3 ]
Noguchi, T. [3 ]
Hosoe, K. [1 ]
机构
[1] Kaneko Corp, Corp Res & Dev Div, Frontier Biochem & Med Res Labs, Takasago, Hyogo 6768688, Japan
[2] Kaneka Corp, Funct Food Ingredients Div, Healthcare Prod Business Unit, Kita Ku, Osaka 5308288, Japan
[3] Japan Ind Safety & Hlth Assoc, Japan Bioassay Res Ctr, Kanagawa 2570015, Japan
关键词
licorice flavonoid oil; LFO; Glycyrrhiza glabra; licorice ethanol extract; genotoxicity;
D O I
10.1016/j.fct.2008.04.008
中图分类号
TS2 [食品工业];
学科分类号
0832 [食品科学与工程];
摘要
Licorice flavonoid oil (LFO) is a new functional food ingredient. In this study, the genotoxicity of LFO was investigated using a test battery of three different methods. In a reverse mutation assay using four Salmonella typhimurium strains and Escherichia coli, LFO did not increase the number of revertant colonies in any tester strain with or without metabolic activation by rat liver S9 mix. In a chromosomal aberration test using Chinese hamster lung (CHL/IU) cells, LFO did not induce any chromosomal aberrations either in the short period test without rat liver S9 mix or in the continuous treatment (24 h or 48 h) test. However, in the short-period test with rat liver S9 mix, LFO induced structural chromosomal aberrations at concentrations higher than 0.6 mg/mL. A bone marrow micronucleus test using male F344 rats was initially conducted. The animals were dosed oral gavage doses up to 5000 mg/kg/day. No significant or dose-dependent increase in the frequency of micronucleated polychromatic erythrocytes (PCE) to total erythrocytes. Subsequently, a liver and peripheral blood micronucleus test using male F344 rats was conducted. No micronuclei induction either in hepatocytes or PCE was observed even at the highest dose of 5000 mg/kg/day. From the findings obtained from the genotoxicity assays performed in this study and the published pharmacokinetic studies of LFO, it appears unlikely that dietary consumption of LFO will present any genotoxic hazard to humans. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2525 / 2532
页数:8
相关论文
共 25 条
[1]
METHODS FOR DETECTING CARCINOGENS AND MUTAGENS WITH SALMONELLA-MAMMALIAN-MICROSOME MUTAGENICITY TEST [J].
AMES, BN ;
MCCANN, J ;
YAMASAKI, E .
MUTATION RESEARCH, 1975, 31 (06) :347-363
[2]
Clinical safety of licorice flavonoid oil (LFO) and pharmacokinetics of glabridin in healthy humans [J].
Aoki, Fumiki ;
Nakagawa, Kaku ;
Kitano, Mitsuaki ;
Ikematsu, Hideyuki ;
Nakamura, Kenjirou ;
Yokota, Shinichi ;
Tominaga, Yuji ;
Arai, Naoki ;
Mae, Tatsumasa .
JOURNAL OF THE AMERICAN COLLEGE OF NUTRITION, 2007, 26 (03) :209-218
[3]
Suppression by licorice flavonoids of abdominal fat accumulation and body weight gain in high-fat diet-induced obese C57BL/6J mice [J].
Aoki, Fumiki ;
Honda, Shinichi ;
Kishida, Hideyuki ;
Kitano, Mitsuaki ;
Arai, Naoki ;
Tanaka, Hozumi ;
Yokota, Shinichi ;
Nakagawa, Kaku ;
Asakura, Tomiko ;
Nakai, Yuji ;
Mae, Tatsumasa .
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 2007, 71 (01) :206-214
[4]
The antioxidative effects of the isoflavan glabridin on endogenous constituents of LDL during its oxidation [J].
Belinky, PA ;
Aviram, M ;
Fuhrman, B ;
Rosenblat, M ;
Vaya, J .
ATHEROSCLEROSIS, 1998, 137 (01) :49-61
[5]
An in vitro screening paradigm for extracts of whole foods for detection of potential toxicants [J].
Charles, GD ;
Linscombe, VA ;
Tornesi, B ;
Mattsson, JL ;
Gollapudi, BB .
FOOD AND CHEMICAL TOXICOLOGY, 2002, 40 (10) :1391-1402
[6]
*ENV HLTH BUR MIN, 1996, GUID DES FOOD ADD RE
[7]
Antiatherosclerotic effects of licorice extract supplementation on hypercholesterolemic patients: Increased resistance of LDL to atherogenic modifications, reduced plasma lipid levels, and decreased systolic blood pressure [J].
Fuhrman, B ;
Volkova, N ;
Kaplan, M ;
Presser, D ;
Attias, J ;
Hayek, T ;
Aviram, M .
NUTRITION, 2002, 18 (03) :268-273
[8]
Licorice extract and its major polyphenol glabridin protect low-density lipoprotein against lipid peroxidation: In vitro and ex vivo studies in humans and in atherosclerotic apolipoprotein E-deficient mice [J].
Fuhrman, B ;
Buch, S ;
Vaya, J ;
Belinky, PA ;
Coleman, R ;
Hayek, T ;
Aviram, M .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1997, 66 (02) :267-275
[9]
Anti-Helicobacter pylori flavonoids from licorice extract [J].
Fukai, T ;
Marumo, A ;
Kaitou, K ;
Kanda, T ;
Terada, S ;
Nomura, T .
LIFE SCIENCES, 2002, 71 (12) :1449-1463
[10]
FUKAI T, 2002, LIFE SCI, V74, P720