1994
DOI: 10.1080/17450399409381767
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Effect of dietary fish oil on serum lipids and lipoproteins of rats fed diets differing in cholesterol and fat

Abstract: The investigation was attempted to clarify the effects of fish oil on the concentration of lipids in serum and lipoproteins in rats fed diets differing in cholesterol and fat. Male Sprague-Dawley rats were maintained on low-fat/high-fat diets without and with 1.5% cholesterol (base diets) for 28 days. Half of each group was then switched to a fish oil diet for 20 days with 5.6% fish oil for exchange of coconut oil and beef tallow. Total cholesterol in rat serum was increased following feeding high amounts of d… Show more

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Cited by 6 publications
(6 citation statements)
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“…The composition of VLDL of geese fed cholesterol and cholic acid, containing more than 70% of cholesterol and only 5% of triglycérides is completely different from normal VLDL which contain predominately triglycérides. There are several investigations with rats (Rönnemaa, 1976;Hulbron et al, 1982;Martins and Dhopeshwarkar, 1982;Huang et al, 1984;Beynen et al, 1986;Stangl et al, 1993Stangl et al, , 1994a, rabbits (Gupta et al, 1976) and monkeys (Myers et al, 1990), which also demonstrated markedly increased concentrations of cholesterol in plasma after feeding diets rich in cholesterol. Most of those investigations did not study isolated lipoproteins; however, a few of them (Beynen et al, 1984;Myers et al, 1990;Stangl et al, 1993Stangl et al, , 1994a demonstrated also cholesterol-enriched VLDL after feeding diets rich in cholesterol.…”
Section: Discussionmentioning
confidence: 92%
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“…The composition of VLDL of geese fed cholesterol and cholic acid, containing more than 70% of cholesterol and only 5% of triglycérides is completely different from normal VLDL which contain predominately triglycérides. There are several investigations with rats (Rönnemaa, 1976;Hulbron et al, 1982;Martins and Dhopeshwarkar, 1982;Huang et al, 1984;Beynen et al, 1986;Stangl et al, 1993Stangl et al, , 1994a, rabbits (Gupta et al, 1976) and monkeys (Myers et al, 1990), which also demonstrated markedly increased concentrations of cholesterol in plasma after feeding diets rich in cholesterol. Most of those investigations did not study isolated lipoproteins; however, a few of them (Beynen et al, 1984;Myers et al, 1990;Stangl et al, 1993Stangl et al, , 1994a demonstrated also cholesterol-enriched VLDL after feeding diets rich in cholesterol.…”
Section: Discussionmentioning
confidence: 92%
“…Several studies in rats (Rönnemaa, 1976;Hulbron et al, 1982;Martins and Dhopeshwarkar, 1982;Beynen et al, 1984;Huang et al, 1984;Garg et al, 1985;Stangl et al, 1993Stangl et al, , 1994a, hamsters (Ohtani et al, 1990) and rabbits (Gupta et al, 1976) demonstrated that diets rich in cholesterol markedly raise plasma cholesterol 286 K. EDER concentrations. Therefore, dietary treatment with cholesterol is a widely used model for the study of the development of atherosclerosis {e.g., Stangl et al, 1993;1994a;Loria and Padgett, 1997;Munilla and Herrera, 1997;Munday et al, 1998).…”
Section: Introductionmentioning
confidence: 95%
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“…It has been well established that supplementation of cholesterol and sodium cholate as hypercholesterolaemic compounds causes an increase in the concentration of cholesterol in plasma, VLDL and LDL, a reduction of cholesterol in HDL and a strong accumulation of cholesterol in the liver [5,42,43] . All these effects were observed in the rats fed the diet supplemented with cholesterol and sodium cholate of experiment 2 compared to those fed the cholesterol-free diet of experiment 1.…”
Section: Discussionmentioning
confidence: 99%
“…As a result of these effects, n‐3 PUFA stimulate β ‐oxidation of fatty acids and inhibit lipogenesis in the liver, resulting in a reduction of liver and plasma TAG concentrations (Sampath and Ntambi, ; Fernandez and West, ). In rodent studies, dietary n‐3 PUFA also caused a reduction of plasma cholesterol concentration (Stangl et al., ; Kawasaki et al., ; Hosomi et al., ). Genes of cholesterol homeostasis, including those involved in cholesterol synthesis and cellular cholesterol uptake, are controlled by SREBP‐2.…”
Section: Introductionmentioning
confidence: 99%