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1.
PLoS One ; 14(3): e0213264, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-30830935

RESUMO

BACKGROUND: As a consequence of indoor occupations and reduced exposure to sunlight, concerns have been raised that vitamin D deficiency is widespread in developed countries. Vitamin D is known to be associated with increased risks of morbidity and mortality in various diseases. OBJECTIVE: To investigate the serum vitamin D status and its relation with life-style factors in pregnant Japanese women. METHODS: Among a cohort for 3,327 pregnant women who participated in an the adjunct study of the Japan Environment and Children's Study during 2011-2013, in which data were obtained on various life-style factors, including both dietary intake of vitamin D and frequency of UV exposure, this study consisted of 1,592 pregnant women, from whom 2,030 serum samples were drawn in Jan, Apr, Jul, and Oct, and the association between serum 25(OH)D level and life-style factors were analyzed using linear mixed models. RESULTS: Serum 25(OH)D levels were less than 20ng/mL in 1,486 of 2,030 samples (73.2%). There was an obvious seasonal change, with serum 25(OH)D levels of less than 20 ng/mL in 89.8% and 47.8% of samples in spring (April) and autumn (October), respectively. Both the frequency spent under sunlight and dietary intake of vitamin D were significantly associated with serum 25(OH)D level. An increase in sunlight exposure of more than 15 min for 1 to 2 days per week in non-winter, or dietary intake of 2 µg/day of vitamin D resulted in an elevation of 1 ng/mL in serum 25(OH)D levels. CONCLUSION: These findings indicate that vitamin D deficiency is very severe in Japanese pregnant women, especially those rarely exposed to sunlight. The benefits of UV rays should also be informed of when its risk is alerted, and clinicians should propose the adequate UV exposure level.


Assuntos
Dieta , Deficiência de Vitamina D/diagnóstico , Vitamina D/administração & dosagem , Adulto , Calcifediol/sangue , Suplementos Nutricionais , Feminino , Humanos , Japão/epidemiologia , Estilo de Vida , Modelos Lineares , Gravidez , Estações do Ano , Inquéritos e Questionários , Raios Ultravioleta , Deficiência de Vitamina D/epidemiologia
2.
J Med Food ; 19(9): 836-43, 2016 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-27540823

RESUMO

The aim of this study was to evaluate the antidiabetic properties of collagen hydrolysates (CHs). CHs exhibited dipeptidyl peptidase-IV inhibitory activity and stimulated glucagon-like-peptide-1 (GLP-1) secretion in vitro. We also determined whether CHs improve glucose tolerance in normal mice. Oral administration of CHs suppressed the glycemic response during the oral and intraperitoneal glucose tolerance tests (OGTT and IPGTT), but the effects were weaker in IPGTT than in OGTT. CHs had no effect on the gastric emptying rate. A pretreatment with the GLP-1 receptor antagonist, exendin 9-39 (Ex9), partially reversed the glucose-lowering effects of CHs, but only when coadministered with glucose. CHs administered 45 min before the glucose load potentiated the glucose-stimulated insulin secretion. This potentiating effect on insulin secretion was not reversed by the pretreatment with Ex9, it appeared to be enhanced. These results suggest that CHs improve glucose tolerance by inhibiting intestinal glucose uptake and enhancing insulin secretion, and also demonstrated that GLP-1 was partially involved in the inhibition of glucose uptake, but not essential for the enhancement of insulin secretion.


Assuntos
Glicemia/metabolismo , Colágeno/farmacologia , Proteínas de Peixes/farmacologia , Peptídeo 1 Semelhante ao Glucagon/sangue , Intolerância à Glucose/sangue , Hipoglicemiantes/farmacologia , Hidrolisados de Proteína/farmacologia , Administração Oral , Animais , Ciclídeos , Colágeno/uso terapêutico , Dipeptidil Peptidase 4/sangue , Inibidores da Dipeptidil Peptidase IV/farmacologia , Proteínas de Peixes/uso terapêutico , Intolerância à Glucose/tratamento farmacológico , Hipoglicemiantes/uso terapêutico , Insulina/metabolismo , Secreção de Insulina , Absorção Intestinal/efeitos dos fármacos , Masculino , Camundongos Endogâmicos C57BL , Hidrolisados de Proteína/uso terapêutico , Valores de Referência
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