The butyrate story: old wine in new bottles?

被引:192
作者
Scheppach, W [1 ]
Weiler, F [1 ]
机构
[1] Univ Wurzburg, Div Gastroenterol, Dept Med, D-97080 Wurzburg, Germany
关键词
butyrate; short-chain fatty acids; dietary fibre; low-digestible carbohydrates; prebiotics; colonic barrier; ulcerative colitis; colorectal cancer;
D O I
10.1097/00075197-200409000-00009
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose of review Short-chain fatty acids are important end products of bacterial carbohydrate fermentation in the colon. In particular, n-butyrate is thought to play a regulatory role in the maintenance of a physiological environment. Disturbances in the interplay between the microflora and the lining epithelium may lead to mucosal inflammation and promote carcinogenesis. The purpose of this article is to review the literature between March 2003 and February 2004 and to determine if recent studies have improved the understanding of butyrate effects in health and disease. Recent findings Preclinical studies (cell culture experiments, animal studies) using modern molecular biological tools (including cDNA arrays) have provided new insights into the action of butyrate on colonic epithelial, vascular endothelial and extracolonic cell types. The new information adds pieces of evidence to the assumption that butyrate may ameliorate colonic inflammation and may be chemopreventive in carcinogenesis. In contrast, new data from clinical studies have been limited in the review period. Summary In the era of molecular biology our understanding of subcellular processes that ultimately lead to inflammatory bowel disease or colorectal cancer has widened considerably. The new powerful technology of genomics and proteomics, however, raises new questions without easy answers. With this new information in mind, we will have to go back to human intervention trials to test the hypotheses generated in vitro. The preclinical data from the review period justify the need for carefully designed clinical trials to test the benefits derived from butyrate production.
引用
收藏
页码:563 / 567
页数:5
相关论文
共 27 条
  • [1] Acetylated, propionylated or butyrylated starches raise large bowel short-chain fatty acids preferentially when fed to rats
    Annison, G
    Illman, RJ
    Topping, DL
    [J]. JOURNAL OF NUTRITION, 2003, 133 (11) : 3523 - 3528
  • [2] Repression of MUC2 gene expression by butyrate, a physiological regulator of intestinal cell maturation
    Augenlicht, L
    Shi, L
    Mariadason, J
    Laboisse, C
    Velcich, A
    [J]. ONCOGENE, 2003, 22 (32) : 4983 - 4992
  • [3] Butyrate is only one of several growth inhibitors produced during gut flora-mediated fermentation of dietary fibre sources
    Beyer-Sehlmeyer, G
    Glei, M
    Hartmann, E
    Hughes, R
    Persin, C
    Böhm, V
    Rowland, I
    Schubert, R
    Jahreis, G
    Pool-Zobel, BL
    [J]. BRITISH JOURNAL OF NUTRITION, 2003, 90 (06) : 1057 - 1070
  • [4] Dietary fibre in food and protection against colorectal cancer in the European Prospective Investigation into Cancer and Nutrition (EPIC): an observational study
    Bingham, SA
    Day, NE
    Luben, R
    Ferrari, P
    Slimani, N
    Norat, T
    Clavel-Chapelon, F
    Kesse, E
    Nieters, A
    Boeing, H
    Tjonneland, A
    Overvad, K
    Martinez, C
    Dorronsoro, M
    Gonzalez, CA
    Key, TJ
    Trichopoulou, A
    Naska, A
    Vineis, P
    Tumino, R
    Krogh, V
    Bueno-de-Mesquita, HB
    Peeters, PHM
    Berglund, G
    Hallmans, G
    Lund, E
    Skeie, G
    Kaaks, R
    Riboli, E
    [J]. LANCET, 2003, 361 (9368) : 1496 - 1501
  • [5] Fructooligosaccharide associated with celecoxib reduces the number of aberrant crypt foci in the colon of rats
    Buecher, B
    Thouminot, C
    Menanteau, J
    Bonnet, C
    Jarry, A
    Heymann, MF
    Cherbut, C
    Galmiche, JP
    Blottière, HM
    [J]. REPRODUCTION NUTRITION DEVELOPMENT, 2003, 43 (04): : 347 - 356
  • [6] P21WAF1/CIP1 is dispensable for G1 arrest, but indispensable for apoptosis induced by sodium butyrate in MCF-7 breast cancer cells
    Chopin, V
    Toillon, RA
    Jouy, N
    Le Bourhis, X
    [J]. ONCOGENE, 2004, 23 (01) : 21 - 29
  • [7] Expression of glutathione S-transferases (GSTs) in human colon cells and inducibility of GSTM2 by butyrate
    Ebert, MN
    Klinder, A
    Peters, WHM
    Schäferhenrich, A
    Sendt, W
    Scheele, J
    Pool-Zobel, BL
    [J]. CARCINOGENESIS, 2003, 24 (10) : 1637 - 1644
  • [8] Butyrate inhibits pancreatic cancer invasion
    Farrow, B
    Rychahou, P
    O'Connor, KL
    Evers, BM
    [J]. JOURNAL OF GASTROINTESTINAL SURGERY, 2003, 7 (07) : 864 - 870
  • [9] Apc+/Min colonic epithelial cells express TNF receptors and ICAM-1 when they are co-cultured with large intestine intra-epithelial lymphocytes
    Forest, V
    Pierre, F
    Bassonga, E
    Meflah, K
    Olivier, C
    Menanteau, J
    [J]. CELLULAR IMMUNOLOGY, 2003, 223 (01) : 70 - 76
  • [10] Expression profiling of CC531 colon carcinoma cells reveals similar regulation of β-catenin target genes by both butyrate and aspirin
    Germann, A
    Dihlmann, S
    Hergenhahn, M
    Doeberitz, MV
    Koesters, R
    [J]. INTERNATIONAL JOURNAL OF CANCER, 2003, 106 (02) : 187 - 197