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Lipids ; 41(9): 835-43, 2006 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-17152920

RESUMO

In humans and animals, intestinal flora is indispensable for bile acid transformation. The goal of our study was to establish gnotobiotic mice with intestinal bacteria of human origin in order to examine the role of intestinal bacteria in the transformation of bile acids in vivo using the technique of gnotobiology. Eight strains of bile acid-deconjugating bacteria were isolated from ex-germ-free mice inoculated with a human fecal dilution of 10(-6), and five strains of 7alpha-dehydroxylating bacteria were isolated from the intestine of limited human flora mice inoculated only with clostridia. The results of biochemical tests and 16S rDNA sequence analysis showed that seven out of eight bile acid-deconjugating strains belong to a bacteroides cluster (Bacteroides vulgatus, B. distasonis, and B. uniformis), and one strain had high similarity with Bilophila wadsworthia. All five strains that converted cholic acid to deoxycholic acid had greatest similarity with Clostridium hylemonae. A combination of 10 isolated strains converted taurocholic acid into deoxycholic acid both in vitro and in the mouse intestine. These results indicate that the predominant bacteria, mainly Bacteroides, in human feces comprise one of the main bacterial groups for the deconjugation of bile acids, and clostridia may play an important role in 7aplha-dehydroxylation of free-form primary bile acids in the intestine although these strains are not predominant. The gnotobiotic mouse with bacteria of human origin could be a useful model in studies of bile acid metabolism by human intestinal bacteria in vivo.


Assuntos
Bactérias/isolamento & purificação , Bactérias/metabolismo , Ceco/microbiologia , Ácido Desoxicólico/metabolismo , Vida Livre de Germes , Animais , Bactérias/classificação , Bacteroides/isolamento & purificação , Bacteroides/metabolismo , Ácido Desoxicólico/biossíntese , Ácido Desoxicólico/química , Feminino , Conteúdo Gastrointestinal/microbiologia , Humanos , Camundongos , Filogenia , Ácido Taurocólico/metabolismo
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