2010
DOI: 10.1055/s-0030-1255021
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Low-Carbohydrate and High-Fat Diets on the Promotion of Hepatic Steatosis in Rats

Abstract: the fat increase in the diet promoted increase of the oxidative stress, evidenced by the decrease in the hepatic concentration of vitamin E, showing its antioxidant role against the probable generated free radicals, the ones which possibly exercised a role in the steatosis occurrence.

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Cited by 16 publications
(13 citation statements)
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“…The excessive consumption of fat was also responsible for the increased glucose in the HF and HPF groups, in agreement with previous studies [42]. Fructosamine is a marker of the levels of glycated serum protein and the levels were smaller in the HF and HPF groups compared with the control group, as the serum fructosamine levels directly reflect the glucose intake by the diet, because the fructosamine concentration may reflect the plasma concentrations of glucose over the last 20 days [43].…”
Section: Discussionsupporting
confidence: 91%
“…The excessive consumption of fat was also responsible for the increased glucose in the HF and HPF groups, in agreement with previous studies [42]. Fructosamine is a marker of the levels of glycated serum protein and the levels were smaller in the HF and HPF groups compared with the control group, as the serum fructosamine levels directly reflect the glucose intake by the diet, because the fructosamine concentration may reflect the plasma concentrations of glucose over the last 20 days [43].…”
Section: Discussionsupporting
confidence: 91%
“…The offer of high-fat diets to rats represents an experimental model for the study of diseases such as NAFLD and metabolic syndrome [20][21][22] . The effects of trans fatty acids on the increase in LDL cholesterol levels and the decrease of HDL cholesterol levels are also well known 23 .…”
Section: Discussionmentioning
confidence: 99%
“…At the end of 30 days, the two groups were sacrificed by decapitation and blood samples were collected for the determination of total serum cholesterol, serum protein and glycemia. The liver was then weighed and placed in liquid nitrogen (-196°C) for later determination of hepatic fat by by Bligh and Dyer extraction 19 . Glycemia, total cholesterol and protein were determined by a colorimetric enzymatic method using a commercial kit (Labtest®, Minas Gerais, Brasil).…”
Section: Methodsmentioning
confidence: 99%