Oral administration of Butyrivibrio fibrisolvens, a butyrate-producing bacterium, decreases the formation of aberrant crypt foci in the colon and rectum of mice

被引:81
作者
Ohkawara, S [1 ]
Furuya, H [1 ]
Nagashima, K [1 ]
Asanuma, N [1 ]
Hino, T [1 ]
机构
[1] Meiji Univ, Coll Agr, Dept Life Sci, Tama Ku, Kawasaki, Kanagawa 2148571, Japan
关键词
Butyrivibrio fibrisolvens; intestinal bacteria; probiotic; colon cancer; butyrate;
D O I
10.1093/jn/135.12.2878
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
Butyrivibrio fibrisolvens, a butyrate-producing ruminal bacterium, was evaluated for use as a probiotic to prevent colorectal cancer. Oral administration to Jcl:ICR mice of a new strain of B. fibrisolvens (MDT-1) that produces butyrate at a high rate (10(9) cfu/dose) increased the rate of butyrate production by fecal microbes, suggesting that MDT-1 can grow in the gut. The number of colorectal aberrant crypt foci (ACIF), putative preneoplastic lesions induced by 1,2-dimethylhydrazine, was reduced after MDT-1 administration (10(9) cfu/dose, 3 times/wk for 4 wk). The number of aberrant crypts (ACs), number of foci having 3 or 4 ACs per focus, and the percentage of mice having 3 or 4 ACs per focus were also reduced, suggesting that the progress of lesions was suppressed by MDT-1. Interestingly, the MDT-1 cell homogenate did not have a similar beneficial effect. MDT-1 had low beta-glucuronidase activity, and administration of MDT-1 reduced the beta-glucuronidase activity in the colorectal contents. The numbers of natural killer (NK) and NKT cells in the spleen were markedly enhanced in response to MDT-1. Decreased beta-glucuronidase activity and increased numbers of NK and NKT cells and butyrate production may explain in part why MDT-1 administration suppressed ACF formation. These results suggest that colorectal cancer may be prevented or suppressed by the utilization of MDT-1 as a probiotic. Administration of MDT-1 had no harmful effect on the health of mice at least for 3 mo.
引用
收藏
页码:2878 / 2883
页数:6
相关论文
共 54 条
[1]  
[Anonymous], 1981, ATLAS RUMEN MICROBIO
[2]   The dietary combination of germinated barley foodstuff plus Clostridium butyricum suppresses the dextran sulfate sodium-induced experimental colitis in rats [J].
Araki, Y ;
Fujiyama, Y ;
Andoh, A ;
Koyama, S ;
Kanauchi, O ;
Bamba, T .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 2000, 35 (10) :1060-1067
[3]   Effects of β-glucuronidase-deficient and lycopene-producing Escherichia coli strains on formation of azoxymethane-induced aberrant crypt foci in the rat colon [J].
Arimochi, H ;
Kataoka, K ;
Kuwahara, T ;
Nakayama, H ;
Misawa, N ;
Ohnishi, Y .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 262 (02) :322-327
[4]   Presence of Butyrivibrio fibrisolvens in the digestive tract of dogs and cats, and its contribution to butyrate production [J].
Asanuma, N ;
Kawato, M ;
Hino, T .
JOURNAL OF GENERAL AND APPLIED MICROBIOLOGY, 2001, 47 (06) :313-319
[5]   The significance of aberrant crypt foci in understanding the pathogenesis of colon cancer [J].
Bird, RP ;
Good, CK .
TOXICOLOGY LETTERS, 2000, 112 :395-402
[6]   Natural killer cells in antiviral defense: Function and regulation by innate cytokines [J].
Biron, CA ;
Nguyen, KB ;
Pien, GC ;
Cousens, LP ;
Salazar-Mather, TP .
ANNUAL REVIEW OF IMMUNOLOGY, 1999, 17 :189-220
[7]  
Bryant M.P., 1986, Bergey's Manual of Systematic Bacteriology, V2, P1376
[8]   INDUCTION OF COLON MUCOSAL BETA-GLUCURONIDASE PRODUCTION AS A MECHANISM FOR 1,2-DIMETHYLHYDRAZINE COLON CARCINOGENESIS [J].
CELIK, C ;
LEWIS, DA ;
MITTLEMAN, A .
JOURNAL OF SURGICAL ONCOLOGY, 1983, 24 (03) :209-211
[9]   IMMUNE MODULATION BY ALTERED NUTRIENT METABOLISM - NUTRITIONAL CONTROL OF IMMUNE-INDUCED GROWTH DEPRESSION [J].
COOK, ME ;
MILLER, CC ;
PARK, Y ;
PARIZA, M .
POULTRY SCIENCE, 1993, 72 (07) :1301-1305
[10]   SHORT CHAIN FATTY-ACIDS IN THE HUMAN-COLON [J].
CUMMINGS, JH .
GUT, 1981, 22 (09) :763-779