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Our objective was to evaluate the influence of body mass index (BMI) on the effects of acute ingestion of different types of fat on the postprandial lipemic response.
The silica particles with very high surface areas due to their porous structure did not impair cell viability or function of macrophages, including the ingestion of different classes of apoptotic or opsonized target cells.
The response of turbine engines to the ingestion of different types of particulate matter will strongly depend on their chemical and physical characteristics, especially at high temperature.
The presumably discontinuous ingestion of different antibiotics at different concentrations may lead to sideeffects similar to health problems resulting from the misuse of antibiotics in humans and domestic animals [1], [22] [24].
This integrated approach may clarify the possible links between satiety and reward effects induced by the ingestion of different dietary sugars.
The protocol adopted for the swallowing assessment involved the ingestion of different food consistencies and was determined by the Radiology Service.
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The effect of pure carbohydrate, protein and fat ingestion on different aspects of short-term satiety and their relation to metabolic and cognitive performance indices were studied in 15 healthy male students.
Our data showed that ingestion rates of different ciliate organisms increased with prey density and the uptake of three bacterial species ranged from 103 to 105 bacteria/ciliate/h, in 106 108 bacteria/ml range concentration.
There was evidence that TnCPV and possibly TnSNPV were activated to overt infections by ingestion of a different virus.
The primary outcome was postprandial plasma responses of GLP-1 measured during and 3 h after ingestion of the different meals (assessed as incremental area under the curve (iAUC)).
The aim of this study was to determine if the minimally modified LDL, obtained after the ingestion of three different diets, produce differential effects on the vascular cell adhesion molecule-1 (VCAM-1) and E-selectin expression in human umbilical endothelial cells (HUVECs).
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