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1.
Nutrients ; 10(4)2018 Apr 04.
Artigo em Inglês | MEDLINE | ID: mdl-29617350

RESUMO

The regular consumption of soy products is associated with inverse incidence of type 2 diabetes, and there has been an increasing interest in the glycemia reducing potential of rice bran and its components. In this study, we investigated whether consuming soymilk with the addition of rice bran (fiber) can reduce the glycemic response of a carbohydrate meal. Seventeen healthy Asian men (BMI: 18.5-29 kg/m²) participated in this randomized crossover trial. On four occasions, they consumed white bread (two times) and white bread with two different soymilks differing in protein and rice bran content. Blood samples were taken to measure glucose and insulin response over a period of 3 hours. Taking the glycemic index (GI) value of white bread as a reference value of 100, the GI of white bread when co-ingested with rice bran soymilk (RBS) was 83.1 (±7.7) and sugar-free soymilk (SFS) was 77.5 (±10.1), both were lower than white bread (p < 0.05). The insulin response of both soymilk treatments was similar to white bread (p > 0.05). The glucose/insulin ratio of RBS and SFS were respectively 43.1 (± 6.1) and 60.0 (± 17.0) and were lower (p < 0.05) than white bread (123.5 ± 21.1) during the first 30 min. In conclusion, co-ingestion of low amounts of soy protein with a carbohydrate meal stimulated early-phase insulin secretion and thereby increased blood glucose clearance effectiveness. Furthermore, rice bran-fortified soymilk reduced the glycemic response similarly to soymilk with a greater dose of soy protein. Rice bran and its components offer therapeutic potential for glycemic and insulinemic control.


Assuntos
Glicemia/metabolismo , Pão , Fibras na Dieta/administração & dosagem , Ingestão de Alimentos , Alimentos Fortificados , Insulina/sangue , Oryza , Sementes , Leite de Soja/administração & dosagem , Adulto , Biomarcadores/sangue , Pão/efeitos adversos , Estudos Cross-Over , Fibras na Dieta/efeitos adversos , Alimentos Fortificados/efeitos adversos , Índice Glicêmico , Humanos , Masculino , Período Pós-Prandial , Singapura , Método Simples-Cego , Fatores de Tempo , Adulto Jovem
2.
FEBS Lett ; 582(15): 2212-8, 2008 Jun 25.
Artigo em Inglês | MEDLINE | ID: mdl-18501710

RESUMO

Chicken muscular dystrophy with abnormal muscle (AM) has been studied for more than 50 years, but the gene responsible for it remains unclear. Our previous studies narrowed down the AM candidate region to approximately 1Mbp of chicken chromosome 2q containing seven genes. In this study, we performed sequence comparison and gene expression analysis to elucidate the responsible gene. One missense mutation was detected in AM candidate genes, while no remarkable alteration of expression patterns was observed. The mutation was identified in WWP1, detected only in dystrophic chickens within several tetrapods. These results suggested WWP1 is responsible for chicken muscular dystrophy.


Assuntos
Galinhas/genética , Distrofia Muscular Animal/genética , Doenças das Aves Domésticas/genética , Ubiquitina-Proteína Ligases/genética , Sequência de Aminoácidos , Animais , Expressão Gênica , Dados de Sequência Molecular , Mutação de Sentido Incorreto
3.
Anim Biotechnol ; 19(2): 122-6, 2008.
Artigo em Inglês | MEDLINE | ID: mdl-18432403

RESUMO

In this study, we describe intraspecies variation in the alphaC connector region of the bovine fibrinogen Aalpha gene. Sequencing and genotyping of six bovine breeds revealed 7 to 10 tandem repeats in the alphaC connector region. In addition, we observed length differences between B. indicus and B. taurus, with the B. indicus having longer fibrinogen alphaC connectors (10-repeat alleles) than B. taurus (7- and 9-repeats). The difference in tandem repeats may be related to the function of blood coagulation system.


Assuntos
Fibrinogênio/genética , Sequências de Repetição em Tandem , Sequência de Aminoácidos , Animais , Sequência de Bases , Bovinos , DNA/química , DNA/genética , Variação Genética , Humanos , Dados de Sequência Molecular , Reação em Cadeia da Polimerase/veterinária , Polimorfismo de Fragmento de Restrição , Alinhamento de Sequência
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