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1.
J Agric Food Chem ; 49(8): 3782-6, 2001 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-11513666

RESUMO

Of the two major brands of baby foods in Canada, one reports lower dietary fiber values than the other, although the products appear to be similar. To investigate the reasons for this discrepancy, seven selected samples of baby foods from both brands were analyzed for total dietary fiber (TDF) according to the Mongeau (rapid Health Protection Branch; HPB) method. Two cereals were also analyzed by using the Prosky and the Englyst (nonstarch polysaccharide; NSP) methods as an internal check on the methodology as well as a means of investigating the reasons for the discrepancies. The sampling included at least four different lots of each product (cereals, fruits, vegetables, and legumes). Each lot was analyzed individually. The TDF values determined using the rapid HPB method were in agreement with those obtained by other dietary fiber methods. Comparison between manufacturer-reported and measured values showed that the low values reported in brand A products were due, in part, to under-reporting of TDF content: measured TDF values were significantly higher than manufacturer-reported values. For brand B products, the manufacturer-reported and measured TDF values were in general agreement. This shows that a large part of the discrepancy between the two brands was due to methodological problems associated with measuring TDF in brand A. Differences in TDF content were also apparent as shown by the fact that brand A TDF values were consistently lower than those of brand B when both were measured by the same method. The differences in TDF content were not explained by differences in the polysaccharide composition of the fiber residues or by differences in water content. Although the limited number of samples does not allow any general conclusion about the TDF content of specific brands, the results show that formulation and/or manufacturing differences may influence TDF values in processed baby foods.


Assuntos
Fibras na Dieta/análise , Alimentos Infantis/análise , Canadá , Análise de Alimentos , Humanos , Lactente
2.
J Nutr ; 117(10): 1708-14, 1987 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-3312521

RESUMO

In ob/ob mice, we showed previously that brown adipose tissue (BAT) has an abnormally low manganese (Mn) content associated with low Mn-superoxide dismutase (MnSOD) and succinate dehydrogenase (SDH) activities. These anomalies can be corrected partially by supplementing the diet with Mn. The present work was designed to find out whether the hypercorticism of the obese mouse plays a role in this anomalous Mn metabolism in BAT. Mn content and MnSOD and SDH activities were determined in BAT from control and adrenalectomized (ADX) obese mice and from control and corticosterone-supplemented lean mice. Adrenalectomy of the obese mouse restored BAT Mn content, SDH activity and lipid peroxidative activity to normal but had little effect on MnSOD activity. Corticosteroid supplementation in the lean mouse did not reproduce the anomalies of Mn metabolism found in the untreated obese mouse. These results show that hypercorticism alone is not responsible for the anomalies of Mn metabolism. It is possible that the hyperinsulinemia of the obese mouse is involved in this process since adrenalectomy corrected hyperinsulinemia in the obese mouse, but corticosteroid supplementation of the lean mouse did not reproduce the high plasma insulin levels or the anomalies in body composition typical of the untreated obese mouse.


Assuntos
Tecido Adiposo Marrom/metabolismo , Hiperfunção Adrenocortical/metabolismo , Manganês/metabolismo , Camundongos Obesos/metabolismo , Adrenalectomia , Hiperfunção Adrenocortical/terapia , Hiperfunção Adrenocortical/veterinária , Animais , Glicemia/metabolismo , Corticosterona/sangue , Insulina/sangue , Peróxidos Lipídicos/biossíntese , Masculino , Camundongos , Camundongos Endogâmicos C57BL/metabolismo , Mitocôndrias/metabolismo , Doenças dos Roedores/metabolismo , Doenças dos Roedores/terapia , Succinato Desidrogenase/metabolismo , Superóxido Dismutase/metabolismo
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