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1.
Am J Physiol Gastrointest Liver Physiol ; 310(6): G367-75, 2016 Mar 15.
Artículo en Inglés | MEDLINE | ID: mdl-26767984

RESUMEN

High-fat diet (HFD)-induced alteration in the gut microbial composition, known as dysbiosis, is increasingly recognized as a major risk factor for various diseases, including colon cancer. This report describes a comprehensive investigation of the effect of agaro-oligosaccharides (AGO) on HFD-induced gut dysbiosis, including alterations in short-chain fatty acid contents and bile acid metabolism in mice. C57BL/6N mice were fed a control diet or HFD, with or without AGO. Terminal restriction fragment-length polymorphism (T-RFLP) analysis produced their fecal microbiota profiles. Profiles of cecal organic acids and serum bile acids were determined, respectively, using HPLC and liquid chromatography-tandem mass spectrometry systems. T-RFLP analyses showed that an HFD changed the gut microbiota significantly. Changes in the microbiota composition induced by an HFD were characterized by a decrease in the order Lactobacillales and by an increase in the Clostridium subcluster XIVa. These changes of the microbiota community generated by HFD treatment were suppressed by AGO supplementation. As supported by the data of the proportion of Lactobacillales order, the concentration of lactic acid increased in the HFD + AGO group. Data from the serum bile acid profile showed that the level of deoxycholic acid, a carcinogenic secondary bile acid produced by gut bacteria, was increased in HFD-receiving mice. The upregulation tended to be suppressed by AGO supplementation. Finally, results show that AGO supplementation suppressed the azoxymethane-induced generation of aberrant crypt foci in the colon derived from HFD-treated mice. Our results suggest that oral intake of AGO prevents HFD-induced gut dysbiosis, thereby inhibiting colon carcinogenesis.


Asunto(s)
Neoplasias del Colon/microbiología , Dieta Alta en Grasa/efectos adversos , Disbiosis/microbiología , Oligosacáridos/farmacología , Sefarosa/farmacología , Animales , Ácidos y Sales Biliares/metabolismo , Clostridium , Fibras de la Dieta , Disbiosis/inducido químicamente , Endotoxinas/sangre , Ácidos Grasos/metabolismo , Heces/microbiología , Lactobacillales , Masculino , Ratones , Ratones Endogámicos C57BL , Microbiota , Obesidad/prevención & control , Oligosacáridos/química , Sefarosa/química
2.
Microbiol Immunol ; 56(11): 729-39, 2012 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-22924537

RESUMEN

Green tea is one of the most popular beverages in the world. Its beneficial health effects and components have been extensively reviewed. However, little is known about the influence of green tea consumption on the human intestinal microbiota (HIM), which plays a crucial role in human health. Ten volunteers who did not usually consume green tea, drank it for 10 days and then stopped drinking it for 7 days. Their fecal samples were collected at three time points: before beginning the 10-day green-tea regime, at the conclusion of that 10 days, and 7 days after stopping the regime. Their fecal samples were analyzed by terminal restriction fragment length polymorphism with specific primer-restriction enzyme systems for HIM and by using a real-time PCR method for the Bifidobacterium species. Although the HIM of each subject was relatively stable, the proportion of Bifidobacterium species played an important role in the classification of their fecal microbiota. Although there were inter-individual differences in the Bifidobacterium species, an overall tendency for the proportion of bifidobacteria to increase because of green tea consumption was noted. However, little change was observed in the composition of Bifidobacterium species in each sample. This suggests that the change in proportion was induced, not by an inter-species transition, but by an intra-species increase and/or decrease. In conclusion, green tea consumption might act as a prebiotic and improve the colon environment by increasing the proportion of the Bifidobacterium species.


Asunto(s)
Carga Bacteriana , Bifidobacterium/aislamiento & purificación , Biota , Tracto Gastrointestinal/microbiología , , Adulto , Anciano , Heces/microbiología , Conducta Alimentaria , Femenino , Experimentación Humana , Humanos , Masculino , Persona de Mediana Edad , Polimorfismo de Longitud del Fragmento de Restricción , Prebióticos , Reacción en Cadena en Tiempo Real de la Polimerasa
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