2018
DOI: 10.1016/j.jff.2018.05.042
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Flaxseed gum reduces body weight by regulating gut microbiota

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Cited by 60 publications
(43 citation statements)
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References 26 publications
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“…Dietary polysaccharides (DPs), both insoluble and soluble, can escape the digestion of human digestive enzyme and reach distal colon, and can be further utilized by gut microbiota and benefit human health (Holscher, 2017; Luo, Li, et al., 2018; Luo, Zhang, et al., 2018; Xie et al., 2019). Different DPs with different compositions and structures may lead to various functions.…”
Section: Introductionmentioning
confidence: 99%
“…Dietary polysaccharides (DPs), both insoluble and soluble, can escape the digestion of human digestive enzyme and reach distal colon, and can be further utilized by gut microbiota and benefit human health (Holscher, 2017; Luo, Li, et al., 2018; Luo, Zhang, et al., 2018; Xie et al., 2019). Different DPs with different compositions and structures may lead to various functions.…”
Section: Introductionmentioning
confidence: 99%
“…In recent years, studies on the mechanisms of the beneficial effects of functional foods have attracted lots of interests (Cabrera, Artacho, & Giménez, ; Huang et al., ; Luo et al., , ; Peng et al., ; Schroeter et al., ; Shahidi, & Ambigaipalan, ). However, reports on the beneficial effects of alternate consumption of bioactive components in traditional Asian diet according to the profile of gut microbes and colonic immunity are rather limited.…”
Section: Discussionmentioning
confidence: 99%
“…The processing and bioinformatics analysis of the 16S rDNA gene sequencing data are performed as described previously (Huang et al., ; Luo et al., ).…”
Section: Methodsmentioning
confidence: 99%
“…The PCR was run with a 20 μl reaction system containing 4 μl of 5 × FastPfu buffer, 2 μl of 2.5 mM dNTPs, 0.8 μl of each primer (5 μM), 0.4 μl of FastPfu polymerase, and 10 ng of template DNA. The thermocycler PCR system was used to perform the PCR (ABI GeneAmp ® 9700) using the following program: denaturation at 95°C for 3 min, then 27 cycles of amplification including denaturation at 95°C for 30 s, annealing at 55°C for 30 s, and extension at 72°C for 45 s, with a final extension at 72°C for 10 min (Luo, Li, et al, ).…”
Section: Methodsmentioning
confidence: 99%
“…The PCR was run with a 20 μl reaction system containing 4 μl of 5 × FastPfu buffer, 2 μl of 2.5 mM dNTPs, 0.8 μl of each primer (5 μM), 0.4 μl of FastPfu polymerase, and 10 ng of template DNA. The thermocycler PCR system was used to perform the PCR (ABI GeneAmp ® 9700) using the following program: denaturation at 95°C for 3 min, then 27 cycles of amplification including denaturation at 95°C for 30 s, annealing at 55°C for 30 s, and extension at 72°C for 45 s, with a final extension at 72°C for 10 min(Luo, Li, et al, 2018b).Amplicons were extracted from 2% agarose gels, purified with the AxyPrep DNA gel extraction kit according to the manufacturer's instructions, and quantified using QuantiFluor™ -ST. According to the standard protocols, the purified amplicons were pooled in equimolar amounts and paired-end sequenced (2 × 250) on an Illumina MiSeq platform.…”
mentioning
confidence: 99%