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1.
Am J Clin Nutr ; 106(3): 747-754, 2017 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-28724643

RESUMO

Background: Many intervention studies have tested the effect of dietary fibers (DFs) on appetite-related outcomes, with inconsistent results. However, DFs comprise a wide range of compounds with diverse properties, and the specific contribution of these to appetite control is not well characterized.Objective: The influence of specific DF characteristics [i.e., viscosity, gel-forming capacity, fermentability, or molecular weight (MW)] on appetite-related outcomes was assessed in healthy humans.Design: Controlled human intervention trials that tested the effects of well-characterized DFs on appetite ratings or energy intake were identified from a systematic search of literature. Studies were included only if they reported 1) DF name and origin and 2) data on viscosity, gelling properties, fermentability, or MW of the DF materials or DF-containing matrixes.Results: A high proportion of the potentially relevant literature was excluded because of lack of adequate DF characterization. In total, 49 articles that met these criteria were identified, which reported 90 comparisons of various DFs in foods, beverages, or supplements in acute or sustained-exposure trials. In 51 of the 90 comparisons, the DF-containing material of interest was efficacious for ≥1 appetite-related outcome. Reported differences in material viscosity, MW, or fermentability did not clearly correspond to differences in efficacy, whereas gel-forming DF sources were consistently efficacious (but with very few comparisons).Conclusions: The overall inconsistent relations of DF properties with respect to efficacy may reflect variation in measurement methodology, nature of the DF preparation and matrix, and study designs. Methods of DF characterization, incorporation, and study design are too inconsistent to allow generalized conclusions about the effects of DF properties on appetite and preclude the development of reliable, predictive, structure-function relations. Improved standards for characterization and reporting of DF sources and DF-containing materials are strongly recommended for future studies on the effects of DF on human physiology. This trial was registered at http://www.crd.york.ac.uk/PROSPERO as CRD42015015336.


Assuntos
Apetite/efeitos dos fármacos , Dieta , Fibras na Dieta , Suplementos Nutricionais , Ingestão de Energia/efeitos dos fármacos , Fibras na Dieta/análise , Fibras na Dieta/farmacologia , Fermentação , Géis , Humanos , Peso Molecular , Viscosidade
2.
Nutrients ; 8(2): 64, 2016 Jan 26.
Artigo em Inglês | MEDLINE | ID: mdl-26821045

RESUMO

Studies show that longer oral exposure to food leads to earlier satiation and lowers energy intake. Moreover, higher energy content of food has been shown to lead to higher satiety. Up to now, it has not been studied systematically how oral exposure duration and gastric energy content interact in satiety regulation. Thirty-seven men (22 ± 4 years, 22 ± 2 kg/m²) participated in a randomized cross-over trial, in which we independently manipulated: (1) oral exposure duration by modified sham feeding (MSF) for 1 or 8 min; and (2) energy content of gastric load (GL) by a nasogastric tube: 100 kcal/500 mL or 700 kcal/500 mL. Outcome measures were appetite ratings and subsequent energy intake from an ad libitum meal. Energy intake was 35% lower after the GLs with 700 kcal than with 100 kcal (p < 0.0001). All appetite ratings were lower in the 700 kcal than in the 100 kcal treatments (area under the curve (AUC); p-values ≤ 0.002); fullness was higher and prospective consumption was lower in the 8 min than in the 1 min MSF treatments (AUC; p-values ≤ 0.02). In conclusion, the current showed that a GL of 700 kcal/500 mL vs. 100 kcal/500 mL increased satiety and lowered energy intake. No additional effects of oral exposure duration could be observed, presumably due to the high contrast in energy between the manipulations. Future research should also focus on the role of oral exposure as such and not only the duration.


Assuntos
Apetite , Ingestão de Energia , Comportamento Alimentar/fisiologia , Conteúdo Gastrointestinal , Boca/fisiologia , Saciação , Estômago , Adolescente , Adulto , Regulação do Apetite , Área Sob a Curva , Índice de Massa Corporal , Estudos Cross-Over , Humanos , Fome , Masculino , Refeições , Período Pós-Prandial , Estudos Prospectivos , Valores de Referência , Adulto Jovem
3.
J Nutr ; 145(2): 365-71, 2015 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-25644360

RESUMO

BACKGROUND: A long oral exposure to food and a high-energy density of food have been shown to increase satiety feelings. The effect of energy density is predominantly caused by an inhibition of gastric emptying. It is hypothesized that prolonging oral exposure may have an additional effect on this inhibition of gastric emptying. However, little human data are available to support this hypothesis. OBJECTIVE: The objective was to assess the effect of the duration of oral exposure to food on gastric emptying rate of gastric loads (GLs) low and high in energy density and on satiety feelings. METHODS: Twenty-six healthy men [mean ± SD age: 22 ± 3 y; BMI (in kg/m(2)): 23 ± 1] participated in a randomized crossover trial with 4 treatments and a control. Treatments consisted of either 1- or 8-min modified sham feeding (MSF) of cake, and a GL of either 100 or 700 kcal infused in the stomach via a nasogastric tube (500 mL, 62.5 mL/min). The control consisted of no MSF and a GL of 500 mL of water. Gastric emptying rate was assessed with a (13)C breath test. Breath samples and satiety feelings were collected at fixed time points until 90 min after start of the treatment. RESULTS: Gastric emptying rate and satiety feelings were not affected by duration of MSF (P ≥ 0.27). However, the 700-kcal GL treatments slowed gastric emptying [41% lower area under the curve (AUC)] and increased satiety feelings (22-31% higher AUC) compared with the 100-kcal GL treatments (P < 0.001). No interaction between MSF duration and energy density of GL was found (P ≥ 0.44). CONCLUSIONS: Higher gastric energy density inhibited gastric emptying and increased satiety feelings in healthy young men. However, prolonging oral exposure to food did not have an additional effect. This study provides more insight in satiety regulation. This trial was registered at trialregister.nl as NTR3601.


Assuntos
Esvaziamento Gástrico/fisiologia , Mucosa Gástrica/metabolismo , Saciação/fisiologia , Adulto , Apetite/fisiologia , Índice de Massa Corporal , Estudos Cross-Over , Ingestão de Energia , Alimentos , Voluntários Saudáveis , Humanos , Masculino , Países Baixos , Fatores de Tempo , Adulto Jovem
4.
Obesity (Silver Spring) ; 20(11): 2226-32, 2012 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-22592331

RESUMO

Appetite is regulated by many factors, including oro-sensory and gastric signals. There are many studies on contributions of and possible interaction between sensory and gastric stimulation, but there are few studies in humans using simultaneous oral and gastric stimulation. We investigated the effect of simultaneous, but independently manipulated, oral and gastric stimulation on appetite ratings and energy intake. We hypothesized that compared with no stimulation, oral and gastric stimulation would equally and additively decrease appetite ratings and energy intake. Healthy men (n = 26, 21 ± 2 years, BMI 22 ± 3 kg/m(2)) participated in a randomized crossover trial with four experimental conditions and a control condition. Experimental conditions consisted of oral stimulation, with either 1 or 8 min modified sham feeding (MSF), and gastric stimulation, with either 100 or 800 ml intragastrically infused liquid (isocaloric, 99 kcal, 100 ml/min). The control condition consisted of no oral or gastric stimulation. Outcome measures were energy intake 30 min after the treatment and appetite ratings. Compared with the control condition, energy intake decreased significantly after the 8 min/100 ml (19% lower, P = 0.001) and 8 min/800 ml conditions (15% lower, P = 0.02), but not after the 1 min/100 ml (14% lower, P = 0.06) and 1 min/800 ml conditions (10% lower, P = 0.39). There was no interaction of oral and gastric stimulation on energy intake. Hunger and fullness differed across all conditions (P ≤ 0.01). In conclusion, duration of oral exposure was at least as important in decreasing energy intake as gastric filling volume. Oral and gastric stimulation did not additively decrease energy intake. Longer oro-sensory stimulation, therefore, may be an important contributor to a lower energy intake.


Assuntos
Apetite/fisiologia , Ingestão de Alimentos/fisiologia , Ingestão de Energia/fisiologia , Saciação/fisiologia , Estômago/fisiologia , Estudos Cross-Over , Humanos , Intubação Gastrointestinal , Masculino , Adulto Jovem
5.
Nutr Rev ; 68(11): 643-55, 2010 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-20961295

RESUMO

The current food supply in many parts of the world differs substantially from that which existed during most of human evolution. It is characterized by a high variety of palatable foods with high energy density and low fiber content. Many foods can be eaten very quickly, and there is not always congruency between the sensory properties of the food and the subsequent metabolic consequences of its ingestion, (e.g., as in the consumption of artificially sweetened foods). It is not presently known how the human body copes with this incongruent food environment in terms of short-term satiety responses and long(er)-term regulation of food intake. Cephalic phase responses (CPRs) are innate and learned physiological responses to sensory signals that prepare the gastrointestinal tract for the optimal processing of ingested foods. CPRs could be affected by inconsistencies in the associations between sensory signals and subsequent post-ingestive consequences. Reviewed here are the available data on how CPRs affect the control of food intake.


Assuntos
Apetite/fisiologia , Encéfalo/fisiologia , Ingestão de Energia/fisiologia , Resposta de Saciedade/fisiologia , Ingestão de Alimentos/fisiologia , Preferências Alimentares/fisiologia , Humanos , Edulcorantes/administração & dosagem , Edulcorantes/efeitos adversos , Paladar/fisiologia
6.
Appetite ; 53(3): 465-8, 2009 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-19800378

RESUMO

This study describes the validation of a new electronic appetite rating system, and a statistical variance model for visual analogue scale (VAS) research. Thirty volunteers rated hunger, fullness, desire to eat, prospective intake, thirst and liking on 100mm paper VAS and on 70 mm electronic VAS presented on a Dell Pocket PC, after consuming breakfast, in a repeated trial. The electronic method was comparable in relative accuracy and reproducibility to the paper method, with weak differences between tests (within-subject SD < or =14 mm). The data obtained were used to generate a model for VAS data variability.


Assuntos
Apetite/fisiologia , Eletrônica , Papel , Adulto , Ingestão de Alimentos/fisiologia , Ingestão de Alimentos/psicologia , Feminino , Humanos , Fome , Masculino , Medição da Dor , Reprodutibilidade dos Testes , Saciação , Sensibilidade e Especificidade , Limiar Sensorial , Inquéritos e Questionários , Sede
7.
Proc Natl Acad Sci U S A ; 101(41): 14830-4, 2004 Oct 12.
Artigo em Inglês | MEDLINE | ID: mdl-15466715

RESUMO

T2R (Tas2R) genes encode a family of G protein-coupled gustatory receptors, several involved in bitter taste perception. So far, few ligands for these receptors have been identified, and the specificity of most T2Rs is unclear. Differences between individual T2Rs result in altered taste perception in either specificity or sensitivity. All 33 human T2Rs are characterized by significant sequence homology. However, with a total of eight pseudogenes and >83 coding region single-nucleotide polymorphisms, the family displays broad diversity. The underlying variability of individual T2Rs might be the source for personalized taste perception. To test this hypothesis and also to identify T2Rs that possibly function beyond bitter taste, we compared all human T2R genes with those of the closely related primate species Pan paniscus (bonobo) and Pan troglodytes (chimpanzee). The differences identified range from large sequence alterations to nonsynonymous and synonymous changes of single base pairs. In contrast to olfactory receptors, no human-specific loss of the amount of functional genes was observed. Taken together, the results indicate ongoing evolutionary diversification of T2R receptors and a role for T2Rs in dietary adaptation and personalized food uptake.


Assuntos
Variação Genética/genética , Receptores Acoplados a Proteínas G/genética , Adenosina , Sequência de Aminoácidos , Animais , Sequência de Bases , Evolução Biológica , DNA/sangue , DNA/genética , DNA/isolamento & purificação , Humanos , Dados de Sequência Molecular , Pan troglodytes , Papio , Alinhamento de Sequência , Deleção de Sequência , Homologia de Sequência do Ácido Nucleico
8.
Cell ; 111(1): 63-75, 2002 Oct 04.
Artigo em Inglês | MEDLINE | ID: mdl-12372301

RESUMO

The dispatched (disp) gene is required for long-range Hedgehog (Hh) signaling in Drosophila. Here, we demonstrate that one of two murine homologs, mDispA, can rescue disp function in Drosophila and is essential for all Hh patterning activities examined in the early mouse embryo. Embryonic fibroblasts lacking mDispA respond normally to exogenously provided Sonic hedgehog (Shh) signal, but are impaired in stimulation of other responding cells when expressing Shh. We have developed a biochemical assay that directly measures the activity of Disp proteins in release of soluble Hh proteins. This activity is disrupted by alteration of residues functionally conserved in Patched and in a related family of bacterial transmembrane transporters, thus suggesting similar mechanisms of action for all of these proteins.


Assuntos
Proteínas de Drosophila/metabolismo , Embrião de Mamíferos/metabolismo , Embrião não Mamífero , Proteínas de Membrana/fisiologia , Transdução de Sinais , Transativadores/metabolismo , Alelos , Motivos de Aminoácidos , Sequência de Aminoácidos , Animais , Transporte Biológico , Padronização Corporal , Membrana Celular/metabolismo , Clonagem Molecular , DNA Complementar/metabolismo , Drosophila , Éxons , Etiquetas de Sequências Expressas , Fibroblastos/metabolismo , Proteínas Hedgehog , Imuno-Histoquímica , Hibridização In Situ , Camundongos , Camundongos Endogâmicos C57BL , Modelos Biológicos , Modelos Genéticos , Dados de Sequência Molecular , Mutação , Crista Neural/patologia , Fenótipo , Prosencéfalo/patologia , Prosencéfalo/ultraestrutura , Homologia de Sequência de Aminoácidos , Fatores de Tempo , beta-Galactosidase/metabolismo
9.
Development ; 129(5): 1119-29, 2002 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-11874908

RESUMO

We have carried out a genetic screen designed to isolate regulators of teashirt expression. One of these regulators is the Grunge gene, which encodes a protein with motifs found in human arginine-glutamic acid dipeptide repeat, Metastasis-associated-like and Atrophin-1 proteins. Grunge is the only Atrophin-like protein in Drosophila, whereas several exist in humans. We provide evidence that Grunge is required for the proper regulation of teashirt but also has multiple activities in fly development. First, Grunge is crucial for correct segmentation during embryogenesis via a failure in the repression of at least four segmentation genes known to regulate teashirt. Second, Grunge acts positively to regulate teashirt expression in proximoventral parts of the leg. Grunge has other regulatory functions in the leg, including the patterning of ventral parts along the entire proximodistal axis and the proper spacing of bristles in all regions.


Assuntos
Proteínas de Drosophila/genética , Drosophila/crescimento & desenvolvimento , Drosophila/genética , Genes de Insetos , Histona Desacetilases , Proteínas Repressoras , Fatores de Transcrição/genética , Sequência de Aminoácidos , Animais , Padronização Corporal , Proteínas de Transporte/genética , Extremidades/embriologia , Dados de Sequência Molecular , Proteínas do Tecido Nervoso/genética , Proteínas/genética , Proteínas Proto-Oncogênicas/genética , Transativadores , Proteína Wnt1
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