scholarly journals Prebiotics Must Achieve a Threshold of Increase in Gut Probiotic Bacteria to Impart Beneficial Health Effects on the Host

2020 ◽  
Vol 4 (Supplement_2) ◽  
pp. 1544-1544
Author(s):  
Breann Abernathy ◽  
Tonya Schoenfuss ◽  
Allison Bailey ◽  
Daniel Gallaher

Abstract Objectives Prebiotic dietary fibers are dietary fibers that] are highly fermented in the large intestine, produce beneficial changes in the gut microbiome, and impart a health benefit to the host. Using reactive extrusion, we have synthesized a novel dietary fiber that is an oligosaccharide of polymerized lactose, which we term polylactose. Here we report on two studies feeding polylactose to rats to determine its prebiotic potential. Methods In Exp. 1, the polylactose preparation contained 51% dietary fiber, 20% free lactose, 5% glucose, and 24% other materials. Rats were fed high fat diets containing 9% total dietary fiber, including cellulose (control, CE, 9%), polylactose (PL, 6%), polydextrose (PD, 6%), and fructooligosaccharide (FOS, 6%). In Exp. 2, the polylactose preparation contained 75% dietary fiber, 9% lactose, 3% glucose, and 13% other materials. Rats were again fed high fat diets containing 9% total dietary fiber, including CE (9%), polylactose (6% or 3%), PD (6%), and galactooligosaccharide (GOS, 6%). In both experiments, rats were fed for 10 weeks, then cecums (empty), cecal contents, livers, and epididymal fat pads were collected. In addition, body composition was determined by MRI. Results In both experiments, final body weight and daily energy intake did not differ among the groups. In Exp. 1, feeding PL greatly increased cecum weight (an indicator of fermentation), cecal Bifidobacterium and Lactobacillus species abundance, increased cecal acetate and propionate, and reduced liver lipids and fat pad weight, compared to the CE group. While PD and FOS increased probiotic species and short chain fatty acids slightly (compared to CE), this was not to the same extent as PL and did not reduce fatty liver and adiposity. In Exp. 2, 6% PL increased cecum weight relative to 3% PF, PD and GOS, all of which were greater than CE. The cecal microbiome was similar among PL (both 3 and 6%), PD, and GOS, all of which differed from CE and were similar to PD and FOS from Exp. 1. Liver lipids, fat pad weight, and body composition did not differ among any of the groups. Conclusions The prebiotic activity of polylactose differed depending on the preparation, for unknown reasons. However, our results suggest there is a threshold of probiotic bacteria abundance that must be attained before beneficial effects are imparted on the host by prebiotics. Funding Sources Midwest Dairy Association.

2014 ◽  
Vol 5 (3) ◽  
pp. 229-239 ◽  
Author(s):  
K. M. Platt ◽  
R. J. Charnigo ◽  
K. J. Pearson

Maternal high-fat diet consumption and obesity have been shown to program long-term obesity and lead to impaired glucose tolerance in offspring. Many rodent studies, however, use non-purified, cereal-based diets as the control for purified high-fat diets. In this study, primiparous ICR mice were fed purified control diet (10–11 kcal% from fat of lard or butter origin) and lard (45 or 60 kcal% fat) or butter (32 or 60 kcal% fat)-based high-fat diets for 4 weeks before mating, throughout pregnancy, and for 2 weeks of nursing. Before mating, female mice fed the 32 and 60% butter-based high-fat diets exhibited impaired glucose tolerance but those females fed the lard-based diets showed normal glucose disposal following a glucose challenge. High-fat diet consumption by female mice of all groups decreased lean to fat mass ratios during the 4th week of diet treatment compared with those mice consuming the 10–11% fat diets. All females were bred to male mice and pregnancy and offspring outcomes were monitored. The body weight of pups born to 45% lard-fed dams was significantly increased before weaning, but only female offspring born to 32% butter-fed dams exhibited long-term body weight increases. Offspring glucose tolerance and body composition were measured for at least 1 year. Minimal, if any, differences were observed in the offspring parameters. These results suggest that many variables should be considered when designing future high-fat diet feeding and maternal obesity studies in mice.


1953 ◽  
Vol 31 (6) ◽  
pp. 474-484
Author(s):  
Denyse D. Duchesne ◽  
Richard Bernard

On choline-free diets containing 10, 18, and 28% casein, the total liver lipids of ducklings were found to be 34.8, 25.0, and 13.8% respectively. Supplementation of the 10% casein diet with 0.5% methionine increased the liver lipids. The same amino acid has no effect at the intermediate level of casein while it is lipotropic at the 28% casein level. In similar experiments with a purified soybean protein (low in methionine) fed at levels of 12, 21.7, and 27.9%, the liver lipids were 31.8, 26.6, and 27.6% respectively. These values do not differ significantly from each other. Methionine was found to be lipotropic at any of these three levels of soybean protein, and more so as the level of the soybean protein increased in the diet. From these results, it is concluded that the purified soybean protein used is a nonlipotropic protein, while casein is definitely lipotropic in ducklings. The lipotropic activity of methionine is closely related to the quality and quantity of the protein in the diet. On high fat diets containing 22, 32, and 42% fat, choline had no lipotropic effect. The average liver lipids for all groups ranged from 11 to 15%. High fat diets are less inducive of fatty livers than high carbohydrate diets. Ducklings fed a fat-free, choline-free basal diet presented livers with an average total lipids of 18%. Supplementing the basal diet with 1% cholesterol increased the liver lipids to 22%. Inositol is lipotropic either in the presence or absence of cholesterol, but choline was much more effective under similar conditions. The two lipotropic factors have a synergistic action and the reduction of the liver lipids is primarily on the glyceride fraction. Cholesteryl ester was at its lowest value in the group fed the basal diet supplemented with inositol only.


2011 ◽  
Vol 105 (12) ◽  
pp. 1750-1763 ◽  
Author(s):  
Gayathri Yepuri ◽  
Helena Marcelino ◽  
Yasaman Shahkhalili ◽  
Olivier Aprikian ◽  
Katherine Macé ◽  
...  

The present study investigates whether excessive fat accumulation and hyperinsulinaemia during catch-up growth on high-fat diets are altered by n-6 and n-3 PUFA derived from oils rich in either linoleic acid (LA), α-linolenic acid (ALA), arachidonic acid (AA) or DHA. It has been shown that, compared with food-restricted rats refed a high-fat (lard) diet low in PUFA, those refed isoenergetically on diets enriched in LA or ALA, independently of the n-6:n-3 ratio, show improved insulin sensitivity, lower fat mass and higher lean mass, the magnitude of which is related to the proportion of total PUFA precursors (LA+ALA) consumed. These relationships are best fitted by quadratic regression models (r2>0·8, P < 0·001), with threshold values for an impact on body composition corresponding to PUFA precursors contributing 25–30 % of energy intake. Isoenergetic refeeding on high-fat diets enriched in AA or DHA also led to improved body composition, with increases in lean mass as predicted by the quadratic model for PUFA precursors, but decreases in fat mass, which are disproportionately greater than predicted values; insulin sensitivity, however, was not improved. These findings pertaining to the impact of dietary intake of PUFA precursors (LA and ALA) and their elongated–desaturated products (AA and DHA), on body composition and insulin sensitivity, provide important insights into the search for diets aimed at counteracting the pathophysiological consequences of catch-up growth. In particular, diets enriched in essential fatty acids (LA and/or ALA) markedly improve insulin sensitivity and composition of weight regained, independently of the n-6:n-3 fatty acid ratio.


2013 ◽  
Author(s):  
Maximilian Bielohuby ◽  
Ayse Zengin ◽  
Amon Horngacher ◽  
Sarina Meurer ◽  
Martin Bidlingmaier

Bone ◽  
2009 ◽  
Vol 45 (6) ◽  
pp. S157
Author(s):  
E. Hernández ◽  
C. Suarez ◽  
A. Ferreira Monteiro ◽  
P. Rodriguez ◽  
M. Gonzáles-Chaves ◽  
...  

Endocrine ◽  
2006 ◽  
Vol 30 (1) ◽  
pp. 69-74 ◽  
Author(s):  
Malgorzata Stachon ◽  
Ewa Fürstenberg ◽  
Joanna Gromadzka-Ostrowska

2012 ◽  
Vol 106 (2) ◽  
pp. 185-192 ◽  
Author(s):  
Samantha J. Caton ◽  
Maximilian Bielohuby ◽  
Yinglong Bai ◽  
Lothar J. Spangler ◽  
Lukas Burget ◽  
...  

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