Protective effect of the bile salt hydrolase-active Lactobacillus reuteri against bile salt cytotoxicity

被引:92
作者
De Boever, P
Wouters, R
Verschaeve, L
Berckmans, P
Schoeters, G
Verstraete, W
机构
[1] State Univ Ghent, Fac Agr & Appl Biol sci, Lab Microbial Ecol & Technol, B-9000 Ghent, Belgium
[2] Vlaamse Instelling Technol Onderzoek, Flemish Inst Technol Res, B-2400 Mol, Belgium
关键词
D O I
10.1007/s002530000330
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Bacterial bile salt hydrolysis is considered a risk factor for the development of colon cancer because of the risk of forming harmful secondary bile salts after an initial deconjugation step. In this study, the influence of enhanced bacterial bile salt transformation by the bile salt hydrolase-active Lactobacillus reuteri was studied in batch culture using the microbial suspension of the Simulator of the Human Intestinal Microbial Ecosystem; (SHIME), which was supplemented with oxgall at 5 g/l or 30 g/l. Changes in the fermentative capacity of the microbial ecosystem and the (geno)toxic properties of the SHIME supernatants were investigated. Increasing concentrations of oxgall inhibited the fermentation. Transient cell toxicity was observed for samples supplemented with 5 g oxgall/l, while samples with 30 g oxgall/l exhibited toxicity. The results of the haemolysis test suggest that the detrimental effects were probably due to the membrane-damaging effects of bile salts. In all cases, the adverse effects could be counteracted by the addition of 7.5 +/- 0.5 log(10) CFU L. reuteri/ml. Plausible mechanisms for the protective properties of L. reuteri could involve a precipitation of the deconjugated bile salts and a physical binding of bile salts by the bacterium, thereby making the harmful bile salts less bioavailable.
引用
收藏
页码:709 / 714
页数:6
相关论文
共 40 条
[31]   Lactobacillus- and Bifidobacterium-mediated antigenotoxicity in the colon of rats [J].
PoolZobel, BL ;
Neudecker, C ;
Domizlaff, I ;
Ji, S ;
Schillinger, U ;
Rumney, C ;
Moretti, M ;
Vilarini, I ;
ScassellatiSforzolini, R ;
Rowland, I .
NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL, 1996, 26 (03) :365-380
[32]  
PRESTONMARTIN S, 1990, CANCER RES, V50, P7415
[33]   Clinical uses of probiotics for stabilizing the gut mucosal barrier: Successful strains and future challenges [J].
Salminen, S ;
Isolauri, E ;
Salminen, E .
ANTONIE VAN LEEUWENHOEK INTERNATIONAL JOURNAL OF GENERAL AND MOLECULAR MICROBIOLOGY, 1996, 70 (2-4) :347-358
[34]   Bile acid-induced alterations of mucin production in differentiated human colon cancer cell lines [J].
Shekels, LL ;
Lyftogt, CT ;
Ho, SB .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 1996, 28 (02) :193-201
[35]  
Singh J, 1997, CANCER RES, V57, P253
[36]   Tocopherols and the etiology of colon cancer [J].
Stone, WL ;
Papas, AM .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1997, 89 (14) :1006-1014
[37]  
VANDELELIE D, 1996, MUTAT RES, V389, P279
[38]  
Vander Plaetse Frank, 1995, Clinical Chemistry, V41, P1906
[39]   DIFFERENTIAL-EFFECTS OF CALCIUM-IONS AND CALCIUM-PHOSPHATE ON CYTOTOXICITY OF BILE-ACIDS [J].
VANDERMEER, R ;
TERMONT, DSML ;
DEVRIES, HT .
AMERICAN JOURNAL OF PHYSIOLOGY, 1991, 260 (01) :G142-G147
[40]   BILE-ACIDS, NEUTRAL STEROIDS, AND BACTERIA IN FECES AS AFFECTED BY A MIXED, A LACTO-OVOVEGETARIAN, AND A VEGAN DIET [J].
VANFAASSEN, A ;
BOL, J ;
VANDOKKUM, W ;
PIKAAR, NA ;
OCKHUIZEN, T ;
HERMUS, RJJ .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1987, 46 (06) :962-967