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1.
J Nutr ; 146(5): 949-56, 2016 05.
Artigo em Inglês | MEDLINE | ID: mdl-27052535

RESUMO

BACKGROUND: Obesity is associated with compromised intestinal barrier function and shifts in gastrointestinal microbiota that may contribute to inflammation. Fiber provides benefits, but impacts of fiber type are not understood. OBJECTIVE: We aimed to determine the impact of cellulose compared with fructans on the fecal microbiota and gastrointestinal physiology in obese mice. METHODS: Eighteen-wk-old male diet-induced obese C57BL/6J mice (n = 6/group; 40.5 g) were fed high-fat diets (45% kcal fat) containing 5% cellulose (control), 10% cellulose, 10% short-chain fructooligosaccharides (scFOS), or 10% inulin for 4 wk. Cecal and colon tissues were collected to assess barrier function, histomorphology, and gene expression. Fecal DNA extracts were subjected to 16S ribosomal RNA amplicon-based Illumina MiSeq sequencing to assess microbiota. RESULTS: Body weight gain was greater (P < 0.05) in scFOS-fed than in 10% cellulose-fed mice. Both groups of fructan-fed mice had greater (P < 0.05) cecal crypt depth (scFOS: 141 µm; inulin: 145 µm) than both groups of cellulose-fed mice (5% and 10%: 109 µm). Inulin-fed mice had greater (P < 0.05) cecal transmural resistance (101 Ω × cm(2)) than 5% cellulose-fed controls (45 Ω × cm(2)). Inulin-fed mice had lower (P < 0.05) colonic mRNA abundance of Ocln (0.41) and Mct1 (0.35) than those fed 10% cellulose (Ocln: 1.28; Mct1: 0.90). Fructan and cellulose groups had different UniFrac distances of fecal microbiota (P < 0.05) and α diversity, which demonstrated lower (P < 0.01) species richness in fructan-fed mice. Mice fed scFOS had greater (P < 0.05) Actinobacteria (15.9%) and Verrucomicrobia (Akkermansia) (17.0%) than 5% controls (Actinobacteria: 0.07%; Akkermansia: 0.08%). Relative abundance of Akkermansia was positively correlated (r = 0.56, P < 0.01) with cecal crypt depth. CONCLUSIONS: Fructans markedly shifted gut microbiota and improved intestinal physiology in obese mice, but the mechanisms by which they affect gut integrity and inflammation in the obese are still unknown.


Assuntos
Bactérias/efeitos dos fármacos , Fibras na Dieta/farmacologia , Frutanos/farmacologia , Microbioma Gastrointestinal/efeitos dos fármacos , Mucosa Intestinal/efeitos dos fármacos , Intestino Grosso/efeitos dos fármacos , Obesidade , Animais , Bactérias/genética , Bactérias/crescimento & desenvolvimento , Celulose/farmacologia , Dieta Hiperlipídica , Fezes/microbiologia , Expressão Gênica , Inflamação/etiologia , Absorção Intestinal , Mucosa Intestinal/metabolismo , Mucosa Intestinal/patologia , Mucosa Intestinal/fisiopatologia , Intestino Grosso/metabolismo , Intestino Grosso/patologia , Intestino Grosso/fisiopatologia , Inulina/farmacologia , Masculino , Camundongos Endogâmicos C57BL , Camundongos Obesos , Transportadores de Ácidos Monocarboxílicos/genética , Transportadores de Ácidos Monocarboxílicos/metabolismo , Obesidade/complicações , Obesidade/microbiologia , Obesidade/fisiopatologia , Ocludina/genética , Ocludina/metabolismo , Oligossacarídeos/farmacologia , Oligossacarídeos/uso terapêutico , RNA Mensageiro/metabolismo , Simportadores/genética , Simportadores/metabolismo , Aumento de Peso/efeitos dos fármacos
2.
J Anim Sci ; 97(3): 1042-1051, 2019 Mar 01.
Artigo em Inglês | MEDLINE | ID: mdl-30649324

RESUMO

Dietary fibers have gained renewed interest in companion animal nutrition as a means to manage pet obesity and improve gut and host health. Soybean hulls (SBH), a coproduct of the soybean oil extraction process, is an accessible and economical fiber source. However, limited research is available on the use of SBH in feline nutrition. Thus, the aim of this study was to determine the effects of a high SBH inclusion level on daily food intake, apparent total tract (ATT) macronutrient digestibility, fecal quality, and fecal fermentative end products in diets of adult cats. Four diets were formulated with either SBH, beet pulp (BP), or cellulose (CL) as the main source of dietary fiber, with the control diet formulated with no added fiber (NF). The fiber treatments were formulated to achieve approximately 15% total dietary fiber (TDF). Eight adult male cats (mean age = 10.5 yr ± 0.1; mean BW = 6.1 ± 0.8 kg) were used in a replicated 4 × 4 Latin square design. Each period consisted of 14 d, with 10 d of diet adaptation followed by 4 d of total fecal and urine collections. Food was offered twice daily and cats were fed to maintain BW. Food intake on a DM basis (DMB) was lower (P < 0.05) in cats fed BP (55.2 g/d) when compared with SBH (70.8 g/d). As-is fecal output did not differ in cats fed BP or SBH, and when expressed on a DMB, fecal output did not differ among fiber treatments. The ATT digestibility of DM, OM, and GE was greater (P < 0.05) in cats fed NF when compared with those fed BP, CL, or SBH. Cats fed CL had the greatest (P < 0.05) ATT CP digestibility (88.5%), followed by cats fed NF (84.9) and SBH (81.7%) with the lowest values (77%) noted for cats fed BP. Acid-hydrolyzed fat (AHF) digestibility was greater for cats fed CL (92.9%) than for cats fed BP (86.9%) and SBH (88.6%). The TDF ATT digestibility was lowest for cats fed NF and CL (8.5% and 15.1%, respectively), followed by SBH (18.0%), with BP having the highest digestibility (33.7%). Total short-chain fatty acid concentration was greatest (P < 0.05) in cats fed BP (699.7 µmole/g) when compared with the other 3 treatments, whereas phenol and indole concentrations did not differ among treatments. In conclusion, a high inclusion level (15% TDF) of SBH appears acceptable in diets for adult cats, resulting in no negative effects on daily food intake, fecal scores, and similar ATT digestibility for most macronutrients when compared with BP and CL.


Assuntos
Ração Animal/análise , Gatos/fisiologia , Fibras na Dieta/administração & dosagem , Digestão/fisiologia , Glycine max , Nutrientes/metabolismo , Animais , Beta vulgaris , Celulose/administração & dosagem , Dieta/veterinária , Digestão/efeitos dos fármacos , Ingestão de Alimentos , Ácidos Graxos Voláteis/análise , Fezes/química , Fermentação/efeitos dos fármacos , Trato Gastrointestinal/efeitos dos fármacos , Trato Gastrointestinal/metabolismo , Masculino
3.
J Anim Sci ; 97(3): 1027-1035, 2019 Mar 01.
Artigo em Inglês | MEDLINE | ID: mdl-30649345

RESUMO

Soybean hulls (SBH) are a fiber-rich co-product of the soybean oil extraction process that corresponds to 8% of the soybean seed. Despite being readily available and priced competitively, SBH are underutilized in monogastric nutrition. Thus, the objective of this study was to evaluate SBH as a dietary fiber in canine diets. Four diets were formulated with either SBH, beet pulp (BP), or cellulose (CL) as the main source of dietary fiber (15% total dietary fiber [TDF]), with the control diet formulated with no supplemental fiber (NF). Animal procedures were approved by the University of Illinois Institutional Animal Care and Use Committee. Eight adult female Beagle (mean age = 4.6 ± 0.6 yr; mean BW = 12.8 ± 1.7 kg) were used in a replicated 4 × 4 Latin square design. Each period consisted of 14 d, with 10 d of diet adaptation followed by 4 d of total fecal and urine collections. At the end of each period, a blood sample was collected and analyzed for serum chemistry. Food was offered twice daily and fed to maintain body weight. Food intake (g/d) on a dry matter basis (DMB) did not differ among treatments. Fecal score was lower (P < 0.05) for dogs fed CL (2.0) in contrast with other dietary treatments (2.3), using a 5-point scale (1 = hard, dry pellets; 5 = diarrhea). Fecal as-is and DM output did not differ for dogs fed BP, CL, or SBH, and were approximately 50% greater (P < 0.05) than dogs fed NF. Apparent total tract digestibility (ATTD) of dry matter, organic matter, and gross energy were greater (P < 0.05) for dogs fed NF when compared with dogs fed BP, CL, or SBH. Dogs fed CL had greater (P < 0.05) AHF ATTD (94%) compared with all other treatments (mean = 91%). Dogs fed CL and NF had greater (P < 0.05) CP ATTD, 87% and 86%, respectively, while dogs fed SBH were intermediate (83%) and dogs fed BP were lowest (79%). Total short-chain fatty acid (SCFA) concentration was greatest in dogs fed BP (582.5 µmol/g) and SBH (479.7 µmol/g) when compared with NF and CL (267.0 and 251.1 µmol/g, respectively). Serum metabolites were within-reference ranges and dogs remained healthy throughout the study. In conclusion, SBH resulted in similar macronutrient ATTD when compared with BP and CL. Dogs fed SBH were also observed to have an increase in fecal SCFA concentration. In general, high level addition of SBH were well-utilized by the dog, resulting in no untoward effects on dog health, nutrient digestibility, or fecal characteristics.


Assuntos
Ração Animal/análise , Fibras na Dieta/administração & dosagem , Digestão , Cães/fisiologia , Glycine max , Nutrientes/metabolismo , Animais , Beta vulgaris , Celulose/administração & dosagem , Dieta/veterinária , Digestão/efeitos dos fármacos , Ingestão de Alimentos , Ácidos Graxos Voláteis/análise , Fezes/química , Feminino , Fermentação/efeitos dos fármacos , Trato Gastrointestinal/efeitos dos fármacos , Trato Gastrointestinal/metabolismo
4.
J Anim Sci ; 97(11): 4519-4531, 2019 Nov 04.
Artigo em Inglês | MEDLINE | ID: mdl-31634399

RESUMO

Prebiotics and dietary fibers are nondigestible ingredients that may confer benefits to the host by selectively stimulating beneficial intestinal bacteria and microbial-derived metabolites that support gut and host health. This experiment evaluated the effects of a blend of prebiotics and dietary fibers on apparent total tract digestibility (ATTD) and fecal metabolites related to gastrointestinal health in adult dogs. Four diets containing either 5% cellulose (control; CT), 5% dietary fiber and prebiotic blend (FP), 0.02% saccharin and eugenol (SE), or 5% fiber blend plus 0.02% saccharin and eugenol (FSE) were formulated to meet or exceed the AAFCO (2017) nutritional requirements for adult dogs. Eight adult female beagles (mean age 4.2 ± 1.1 yr; mean BW = 10.8 ± 1.4 kg; mean BCS = 5.8 ± 0.6) were randomly assigned to 1 of the 4 dietary treatments using a replicated 4 × 4 Latin square design. Each experimental period consisted of 14 d (10 d of diet adaptation and 4 d of total and fresh fecal and total urine collection). All animals remained healthy throughout the study, with serum metabolites being within reference ranges for adult dogs. All diets were well accepted by the dogs, resulting in similar (P > 0.05) daily food intakes among treatments. Likewise, fecal output and scores did not differ (P > 0.05) among dietary treatments, with the latter being within the ideal range (2.5-2.9) in a 5-point scale. All diets were highly digestible and had similar (P > 0.05) ATTD of dry matter (81.6%-84.4%), organic matter (86.4%-87.3%), and crude protein (86.6%-87.3%). However, total dietary fiber (TDF) digestibility was greater for dogs fed the FSE diet (P < 0.05) in contrast with dogs fed the CT and SE diets, whereas dogs fed FP diets had intermediate TDF digestibility, but not different from all other treatments. Fecal acetate and propionate concentrations were greater (P < 0.05) for dogs fed FP and FSE diets. Fecal concentrations of isobutyrate and isovalerate were greater for dogs fed CT (P < 0.05) compared with dogs fed the other three treatments. No shifts in fecal microbial richness and diversity were observed among dietary treatments. Overall, the data suggest that dietary supplementation of fiber and prebiotic blend was well tolerated by dogs, did not cause detrimental effects on fecal quality or nutrient digestibility, and resulted in beneficial shifts in fecal metabolites that may support gut health.


Assuntos
Fibras na Dieta/administração & dosagem , Suplementos Nutricionais/análise , Cães/fisiologia , Eugenol/administração & dosagem , Microbioma Gastrointestinal , Prebióticos/administração & dosagem , Ração Animal/análise , Animais , Celulose/metabolismo , Dieta/veterinária , Digestão/efeitos dos fármacos , Fezes/química , Fezes/microbiologia , Feminino , Trato Gastrointestinal/metabolismo , Trato Gastrointestinal/microbiologia , Nutrientes/administração & dosagem , Distribuição Aleatória , Sacarina/administração & dosagem
5.
JPEN J Parenter Enteral Nutr ; 33(6): 607-17; discussion 617, 2009.
Artigo em Inglês | MEDLINE | ID: mdl-19892901

RESUMO

BACKGROUND: Glucose transporter 2 (GLUT2) is a high-capacity, facilitative intestinal monosaccharide transporter, known to be upregulated by short-chain fatty acids (SCFAs) derived from the intestinal microbiota during fermentation. Understanding the mechanisms regulating intestinal function is important to optimize therapies for patients with intestinal failure and ultimately reduce their dependence on parenteral nutrition. OBJECTIVE: The objective was to examine the mechanism regulating the underlying response of GLUT2 to the SCFA butyrate. METHODS: GLUT2 messenger RNA (mRNA) abundance was measured in differentiated Caco2-BBe monolayers treated for 0.5-24 hours with 0-20 mM butyrate using quantitative reverse transcription-polymerase chain reaction. Activation of the human GLUT2 promoter was measured using luciferase reporting in transiently transfected Caco2-BBe monolayers. RESULTS: GLUT2 mRNA abundance was higher (P < .0001) with 1-4 hours of exposure to 2.5, 7.5, and 10 mM butyrate. Butyrate induced (P < .0001) promoter activity in a dose-dependent fashion. Analysis of the GLUT2 promoter indicated that regions -282/+522, -216/+522, and -145/+522 had a heightened (P < .05) response to butyrate compared with 1135/+522 and 564/+522. CONCLUSIONS: Butyrate upregulates GLUT2 mRNA abundance in Caco2-BBe monolayers by activating specific regions within the human GLUT2 promoter. These results identify a cellular mechanism wherein butyrate upregulates intestinal absorption that may be relevant to patients with reduced function. Additional work is necessary to understand cellular targets of butyrate therapy and define clinically appropriate means of providing such strategies, such as consuming prebiotics and probiotics.


Assuntos
Butiratos/farmacologia , Regulação da Expressão Gênica , Transportador de Glucose Tipo 2/metabolismo , Regiões Promotoras Genéticas/efeitos dos fármacos , Ativação Transcricional , Células CACO-2 , Relação Dose-Resposta a Droga , Transportador de Glucose Tipo 2/genética , Humanos , RNA Mensageiro/metabolismo , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Regulação para Cima
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