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
[11]  
Cummings JH, 1991, LARGE INTESTINE PHYS, P51
[12]  
DELZENNE NM, 1994, FOOD SCI TECHNOL-LEB, V27, P1, DOI 10.1006/fstl.1994.1001
[13]   The innate immune response to tumors and its role in the induction of T-cell immunity [J].
Diefenbach, A ;
Raulet, DH .
IMMUNOLOGICAL REVIEWS, 2002, 188 :9-21
[14]   Alternative schemes of butyrate production in Butyrivibrio fibrisolvens and their relationship to acetate utilization, lactate production, and phylogeny [J].
Diez-Gonzalez, F ;
Bond, DR ;
Jennings, E ;
Russell, JB .
ARCHIVES OF MICROBIOLOGY, 1999, 171 (05) :324-330
[15]   A new strain of Butyrivibrio fibrisolvens that has high ability to isomerize linoleic acid to conjugated linoleic acid [J].
Fukuda, S ;
Furuya, H ;
Suzuki, Y ;
Asanuma, N ;
Hino, T .
JOURNAL OF GENERAL AND APPLIED MICROBIOLOGY, 2005, 51 (02) :105-113
[16]  
FULLER R, 1989, J APPL BACTERIOL, V66, P365
[17]   Oral administration of arabinogalactan affects immune status and fecal microbial populations in dogs [J].
Grieshop, CM ;
Flickinger, EA ;
Fahey, GC .
JOURNAL OF NUTRITION, 2002, 132 (03) :478-482
[18]  
HA YL, 1990, CANCER RES, V50, P1097
[19]   Butyrate acts as a survival factor for colonic epithelial cells: Further fuel for the in vivo versus in vitro debate [J].
Hague, A ;
Singh, B ;
Paraskeva, C .
GASTROENTEROLOGY, 1997, 112 (03) :1036-1040
[20]   NATURAL CYTOTOXIC REACTIVITY OF MOUSE LYMPHOID-CELLS AGAINST SYNGENEIC AND ALLOGENEIC TUMORS .1. DISTRIBUTION OF REACTIVITY AND SPECIFICITY [J].
HERBERMAN, RB ;
NUNN, ME ;
LAVRIN, DH .
INTERNATIONAL JOURNAL OF CANCER, 1975, 16 (02) :216-229