Genotoxicity testing of a Salacia oblonga extract

被引:20
作者
Flammang, A. M.
Erexson, G. L.
Mecchi, M. S.
Murli, H.
机构
[1] Abbott Labs, Ross Prod Div, Columbus, OH 43215 USA
[2] Covance Labs Inc, Vienna, VA 22182 USA
关键词
Salacia oblonga; alpha-glucosidase inhibitor; toxicology; safety; reverse mutation assay; chromosomal aberration assay; mouse micronucleus assay;
D O I
10.1016/j.fct.2006.06.005
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Salacia oblonga has been used for thousands of years in Ayurvedic medicine for the oral treatment of diabetes. The root extract has been shown to inhibit the activity of intestinal alpha-glucosidases, therefore S. oblonga holds potential as a natural method to mitigate the blood glucose response for people with diabetes. As part of a safety evaluation of novel ingredients for use in blood glucose control, the potential genotoxicity of a S. oblonga root extract (SOE) was evaluated using the standard battery of tests (reverse mutation assay; chromosomal aberrations assay; mouse micronucleus assay) recommended by US Food and Drug Administration (FDA) for food ingredients. SOE was determined not to be genotoxic under the conditions of the reverse mutation assay and mouse micronucleus assay, and weakly positive for the chromosomal aberrations assay. A reproducible, although weak, positive chromosomal aberrations response in human lymphocytes is of concern and further toxicity research is recommended. Use of SOE is presently expected to be safe, as anticipated intake is small compared to the doses administered in the genotoxicity assays and may, after further toxicity research, may prove be a useful ingredient in foodstuffs. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1868 / 1874
页数:7
相关论文
共 16 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]  
[Anonymous], 1971, Statistical Principles in Experimental Design
[3]  
EVANS HJ, 1962, INT REV CYTOL, V13, P221
[4]  
Evans HJ., 1976, CHEMICAL MUTAGENS PR, P1, DOI DOI 10.1007/978-1-4684-0892-8_1
[5]   REPORT FROM WORKING GROUP ON IN-VITRO TESTS FOR CHROMOSOMAL-ABERRATIONS [J].
GALLOWAY, SM ;
AARDEMA, MJ ;
ISHIDATE, M ;
IVETT, JL ;
KIRKLAND, DJ ;
MORITA, T ;
MOSESSO, P ;
SOFUNI, T .
MUTATION RESEARCH, 1994, 312 (03) :241-261
[6]   Synthesis of nitrogen analogues of salacinol and their evaluation as glycosidase inhibitors [J].
Ghavami, A ;
Johnston, BD ;
Jensen, MT ;
Svensson, B ;
Pinto, BM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (26) :6268-6271
[7]   MUTAGEN TESTING USING TRP+ REVERSION IN ESCHERICHIA-COLI [J].
GREEN, MHL ;
MURIEL, WJ .
MUTATION RESEARCH, 1976, 38 (01) :3-32
[8]   Medicinal plants of India with anti-diabetic potential [J].
Grover, JK ;
Yadav, S ;
Vats, V .
JOURNAL OF ETHNOPHARMACOLOGY, 2002, 81 (01) :81-100
[9]   REVISED METHODS FOR THE SALMONELLA MUTAGENICITY TEST [J].
MARON, DM ;
AMES, BN .
MUTATION RESEARCH, 1983, 113 (3-4) :173-215
[10]  
Matsuda H., 2005, Journal of Traditional Medicines, V22, P145