Toxicological evaluation of neoagarooligosaccharides prepared by enzymatic hydrolysis of agar

被引:32
作者
Hong, Sun Joo [1 ,2 ]
Lee, Je-Hyeon [2 ]
Kim, Eun Joo [2 ]
Yang, Hea Jung [2 ]
Park, Jae-Seon [1 ]
Hong, Soon-Kwang [1 ]
机构
[1] Myongji Univ, Dept Biol Sci & Bioinformat, 116 Myongji Ro, Yongin 17058, Gyeonggido, South Korea
[2] Dynebio Inc, B B205 Woolimlions Valley 2,45 Sagimagil Ro, Seongnam Si 13209, Gyeonggi Do, South Korea
关键词
NAOs (neoagarooligosaccharides); Acute toxicity; Subchronic toxicity; Genotoxicity; Agar; MICRONUCLEUS TEST; BETA-AGARASE; OLIGOSACCHARIDES; GENOTOXICITY;
D O I
10.1016/j.yrtph.2017.08.001
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
Agar, a heterogeneous polymer of galactose, is the main component of the cell wall of marine red algae. It is well established as a safe, non-digestible carbohydrate in Oriental countries. Although neoagarooligosaccharides (NAOs) prepared by the hydrolysis of agar by beta-agarase have been reported to exert various biological activities, the safety of these compounds has not been reported to date. For safety evaluation, NAOs containing mainly neoagarotetraose and neoagarohexaose were prepared from agar by enzymatic hydrolysis using beta-agarase DagA from Streptomyces coelicolor. Genotoxicity tests such as the bacterial reverse mutation assay, eukaryotic chromosome aberration assay, and in vivo micronucleus assay all indicated that NAOs did not exert any mutational effects. The toxicity of NAOs in rat and beagle dog models was investigated by acute, 14-day, and 91-day repeated oral dose toxicity tests. The results showed that NAO intake of up to 5,000 mg/kg body weight resulted in no significant changes in body weight, food intake, water consumption, hematologic and blood biochemistry parameters, organ weight, or clinical symptoms. Collectively, a no-observed-adverse-effect level of 5,000 mg/kg body weight/day for both male and female rats was established for NAO. These findings support the safety of NAO for possible use in food supplements and pharmaceutical and cosmetic products. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:9 / 21
页数:13
相关论文
共 25 条
[1]   Antioxidant activity and hepatoprotective potential of agaro-oligosaccharides in vitro and in vivo [J].
Chen, Haimin ;
Yan, Xiaojun ;
Zhu, Peng ;
Lin, Jing .
NUTRITION JOURNAL, 2006, 5 (1)
[2]   Agar degradation by microorganisms and agar-degrading enzymes [J].
Chi, Won-Jae ;
Chang, Yong-Keun ;
Hong, Soon-Kwang .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2012, 94 (04) :917-930
[3]   Pre-clinical safety evaluation of the synthetic human milk, nature-identical, oligosaccharide 2′-O-Fucosyllactose (2′FL) [J].
Coulet, Myriam ;
Phothirath, Phoukham ;
Allais, Linda ;
Schilter, Benoit .
REGULATORY TOXICOLOGY AND PHARMACOLOGY, 2014, 68 (01) :59-69
[4]   Anti-tumor-Promoting Activities of Agaro-Oligosaccharides on Two-Stage Mouse Skin Carcinogenesis [J].
Enoki, Tatsuji ;
Tominaga, Takanari ;
Takashima, Fuyuko ;
Ohnogi, Hiromu ;
Sagawa, Hiroaki ;
Kato, Ikunoshin .
BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2012, 35 (07) :1145-1149
[5]   Agarase: Review of Major Sources, Categories, Purification Method, Enzyme Characteristics and Applications [J].
Fu, Xiao Ting ;
Kim, Sang Moo .
MARINE DRUGS, 2010, 8 (01) :200-218
[6]   REPORT OF THE INTERNATIONAL WORKSHOP ON STANDARDIZATION OF GENOTOXICITY TEST PROCEDURES - COMMENT [J].
GALLOWAY, SM .
MUTATION RESEARCH, 1994, 312 (03) :201-203
[7]  
Giordano Assurita, 2006, Biotechnology Journal, V1, P511, DOI 10.1002/biot.200500036
[8]  
Greene M., 1984, Hegel and the sciences, P161
[9]  
Han Zhong-Ze, 2010, Laboratory Animal Research, V26, P153
[10]   AN APPLICATION OF ACRIDINE-ORANGE FLUORESCENT STAINING TO THE MICRONUCLEUS TEST [J].
HAYASHI, M ;
SOFUNI, T ;
ISHIDATE, M .
MUTATION RESEARCH, 1983, 120 (04) :241-247