Genotoxicity and subchronic toxicity studies of DHA-rich oil in rats

被引:28
作者
Blum, Rene [1 ]
Kiy, Thomas [1 ]
Tanaka, Satohiro [2 ]
Wong, Andrea W. [3 ]
Roberts, Ashley [3 ]
机构
[1] Lonza Grp Ltd, CH-4002 Basel, Switzerland
[2] Nagase Chemtex, Nishi Ku, Osaka 5508668, Japan
[3] Cantox Hlth Sci Int, Mississauga, ON L5N 2X7, Canada
关键词
DHA-rich oil; omega-3 polyunsaturated fatty acid; docosahexaenoic acid; DHA; toxicity; safety; subchronic; genotoxicity; food ingredient; marine protist;
D O I
10.1016/j.yrtph.2007.08.005
中图分类号
DF [法律]; D9 [法律]; R [医药、卫生];
学科分类号
0301 ; 10 ;
摘要
Polyunsaturated fatty acids, including docosahexaenoic acid (DHA), are natural constituents of the human diet. DHA-algal oil is produced through the use of the non-toxigenic and non-pathogenic marine protist, Ulkenia sp. The safety of DHA-algal oil was assessed in a subchronic toxicity study and in genotoxicity studies. In a 90-day study, rats were orally administered water or DHA-algal oil at concentrations of 0, 500, 1000, and 2000 mg/kg in combination with 2000, 1500, 1000 or 0 mg/kg DHA-containing fish oil, respectively. Additional animals were administered water, 2000 mg/kg DHA-algal oil, or 2000 mg/kg fish oil for 90 days, followed by a 4-week recovery phase. No treatment-related effects were observed in clinical observations, food and water consumption, mortality, gross pathology, and histopathology. Increased body weights and liver weights in oil-treated groups were attributed to the large lipid load and were not regarded as toxicologically significant. Furthermore, no treatment-related differences in the measured parameters between the DHA-algal oil and fish oil groups were detected. In genotoxicity experiments, DHA-algal oil exerted no mutagenic activity in various bacterial strains, nor did it induce chromosomal aberrations in Chinese hamster fibroblast cells. These results support the safety of DHA-algal oil as a dietary source of DHA. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:271 / 284
页数:14
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