2019
DOI: 10.1016/j.foodchem.2019.04.063
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Colonic fermentation of water soluble fiber fraction extracted from sugarcane (Sacchurum officinarum L.) bagasse in murine models

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Cited by 19 publications
(11 citation statements)
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“…In the last decade, several investigations have focused on investigating the impact of pre-digested isolated fractions of foods or beverages on the intestinal microbiota during colonic fermentation. Studies include use of black tea and red wine [14], kiwifruit [15], pomegranate [16], apple varieties [11] and sugarcane [17]. These have reported a specific alteration on the structure and dynamics of the intestinal microbiota community, which are dependent on the isolated fraction source.…”
Section: Introductionmentioning
confidence: 99%
“…In the last decade, several investigations have focused on investigating the impact of pre-digested isolated fractions of foods or beverages on the intestinal microbiota during colonic fermentation. Studies include use of black tea and red wine [14], kiwifruit [15], pomegranate [16], apple varieties [11] and sugarcane [17]. These have reported a specific alteration on the structure and dynamics of the intestinal microbiota community, which are dependent on the isolated fraction source.…”
Section: Introductionmentioning
confidence: 99%
“…After acclimatization for one week on a commercial diet (Standard powder diet for mouse, rat, hamster, Oriental Yeast Co.) rats were grouped into four similar body weight groups (≃187 g). Following grouping, rats were cared and maintained as previously mentioned in Pelpolage et al [ 24 ] with free access to experimental diets (≃25 g) and ad libitum water (≃150 mL). The cages were maintained at 23 ± 1 °C temperature and 60 ± 5% relative humidity under a 12 h light/dark cycle and each rat was individually housed.…”
Section: Methodsmentioning
confidence: 99%
“…Extraction of bacterial DNA from the cecal content samples (stored at −80 °C) by modified phenol-free repeated bead beating plus column (RBB + C) method, purification of extracted genomic DNA (QIAamp DNA Stool Mini Kit, QIAGEN, Valencia, CA, USA) and measurement of concentration of extracted community DNA (Nano Drop 2000c spectrophotometer, Thermo Fisher Scientific, Tokyo, Japan) were conducted as previously mentioned [ 24 ]. Finally, the extracted and purified genomic DNA concentration was adjusted to 5 ng/µL with Tris-EDTA buffer.…”
Section: Methodsmentioning
confidence: 99%
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