Abstract:BackgroundFoods that enhance satiety can help consumers to resist environmental cues to eat, and improve the nutritional quality of their diets. Viscosity generated by oat β-glucan, influences gastrointestinal mechanisms that mediate satiety. Differences in the source, processing treatments, and interactions with other constituents in the food matrix affect the amount, solubility, molecular weight, and structure of the β-glucan in products, which in turn influences the viscosity. This study examined the effect… Show more
“…Thus, vagal nerve stimulation from other regions of the digestive tract, such as stomach and small intestine, are more likely contributors to modulating diet intake, especially when barley b-glucan can increase digesta viscosity in the upper gut (Brockman et al 2012) and tends to slow the rate of gastric emptying (Belobrajdic et al 2015). These observations align with clinical studies which showed that oat b-glucan increased perceptions of satiety during the postprandial period Juvonen et al 2009;Lyly et al 2010;Pentikainen et al 2014;Rebello et al 2013Rebello et al , 2014 and modulated the secretion of satiety hormones in the small intestine, including cholecystokinin, ghrelin and peptide YY Vitaglione et al 2009). Therefore, b-glucan fermentation in the large bowel is unlikely to contribute to reduced energy intake and body weight.…”
Using barley cultivars differing widely in β-glucan content, we aimed to determine their effects on small intestinal macronutrient digestion in 24 ileorectostomised rats. The rats were fed 1 of 4 experimental diets, each containing a different barley variety, for 11 d. The diets had a content of 0, 2.1, 2.6 and 4.3 g of β-glucan/100 g. Feed intake and faecal excretion of fat, protein, starch, and non-starch polysaccharides were determined in the final 5 d of the study and apparent macronutrient digestibility calculated. Higher dietary levels of β-glucan (2.6% and 4.3%) lowered feed intake (by 15 and 19%, respectively) but final body weight was only lowered by the 4.3% β-glucan diet relative to rats fed the 0% β-glucan diet (all ps < 0.05). Protein, lipid and starch digestibility was unrelated to the dietary β-glucan content. Higher dietary levels of barley β-glucan lower feed intake of ileorectostomised rats, which is independent of intestinal fermentation and unrelated to macronutrient digestibility.
“…Thus, vagal nerve stimulation from other regions of the digestive tract, such as stomach and small intestine, are more likely contributors to modulating diet intake, especially when barley b-glucan can increase digesta viscosity in the upper gut (Brockman et al 2012) and tends to slow the rate of gastric emptying (Belobrajdic et al 2015). These observations align with clinical studies which showed that oat b-glucan increased perceptions of satiety during the postprandial period Juvonen et al 2009;Lyly et al 2010;Pentikainen et al 2014;Rebello et al 2013Rebello et al , 2014 and modulated the secretion of satiety hormones in the small intestine, including cholecystokinin, ghrelin and peptide YY Vitaglione et al 2009). Therefore, b-glucan fermentation in the large bowel is unlikely to contribute to reduced energy intake and body weight.…”
Using barley cultivars differing widely in β-glucan content, we aimed to determine their effects on small intestinal macronutrient digestion in 24 ileorectostomised rats. The rats were fed 1 of 4 experimental diets, each containing a different barley variety, for 11 d. The diets had a content of 0, 2.1, 2.6 and 4.3 g of β-glucan/100 g. Feed intake and faecal excretion of fat, protein, starch, and non-starch polysaccharides were determined in the final 5 d of the study and apparent macronutrient digestibility calculated. Higher dietary levels of β-glucan (2.6% and 4.3%) lowered feed intake (by 15 and 19%, respectively) but final body weight was only lowered by the 4.3% β-glucan diet relative to rats fed the 0% β-glucan diet (all ps < 0.05). Protein, lipid and starch digestibility was unrelated to the dietary β-glucan content. Higher dietary levels of barley β-glucan lower feed intake of ileorectostomised rats, which is independent of intestinal fermentation and unrelated to macronutrient digestibility.
“…There is growing evidence to suggest that oat β-glucan increases satiety (Beck, et al 2009; Geliebter, et al 2015; Geliebter, et al 2014; Juvonen, et al 2009; Lyly, et al 2010; Pentikainen, et al 2014; Rebello, et al 2014; Rebello, et al 2013) and reduces post-prandial glycemia (Tosh 2013). The most likely mechanism is the viscosity generated in the gastrointestinal tract which has physiologic responses such as delayed gastric emptying, increased stomach distension, delayed intestinal transit, and reduced absorption of nutrients.…”
Section: Discussionmentioning
confidence: 99%
“…Some of these effects are satiety signals that inhibit hunger after a meal is eaten (Blundell, et al 1996). There is substantial evidence to suggest that oat β-glucan increases satiety (Beck, et al 2009; Geliebter, et al 2015; Geliebter, et al 2014; Juvonen, et al 2009; Lyly, et al 2010; Pentikainen, et al 2014; Rebello, et al 2014; Rebello, et al 2013) and that oat products reduce the human glycemic response, compared to similar wheat foods or a glucose control (Tosh 2013). Further, certain polyphenols such as the anthocyanins found in berries exhibit an insulin-like effect to influence starch degradation and thereby the post meal blood glucose response (McDougall and Stewart 2005).…”
Objective
The objective of this study was to examine the effects of a gastrointestinal microbiome modulator (GIMM) containing inulin, β-glucan, blueberry anthocyanins, and blueberry polyphenols on metabolic parameters, fecal markers of gut microbiota, and satiety.
Design and Methods
Thirty overweight or obese individuals aged 18 to 70 years, were enrolled in a randomized controlled trial. Participants consumed the test product or placebo daily for four weeks. Stool samples were collected and blood was drawn at baseline and week four for assessments of gut microbiota, satiety hormones, glucose control, and lipid measures. Subjective satiety was assessed weekly. Linear models were used to compare differences from baseline to week four.
Results
GIMM consumption improved blood glucose tolerance (p = 0.008), and increased satiety (p = 0.03). There were no statistically significant differences in insulin sensitivity, fecal markers of gut microbiota, plasma satiety hormones, or serum lipid concentrations between the groups. However, plasma satiety hormones and fecal short chain fatty acid concentrations increased in the test group compared to the placebo.
Conclusions
GIMM consumption for four weeks, increases satiety, and improves glucose tolerance possibly through insulin-independent pathways.
“…The oat flakes presented the highest swelling and the largest particle size (Table 2). In addition, whatever the kilning and flaking processes, they contain β-glucan, a major component of oat endosperm cell walls, which probably immobilized some water during the batter preparation and pie baking (Rebello et al, 2014), contributing a drier, harder texture. In fact TPA hardness and chewiness, and Fmax and deformability from the penetration test appeared very near in the same quadrant (Fig.…”
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