Abnormal cholesterol uptake, storage, and synthesis in the livers of 2-acetylaminofluorene-fed rats.
BJ Horton, Jeanette D. Horton, Henry C. Pitot
Abstract
BJ Horton, Jeanette D. Horton, Henry C. Pitot
Abstract
Summary Rat livers were tested for both rate of cholesterol synthesis and uptake of a p.o. dose of cholesterol- 3 H after rats were fed 0.06% 2-acetylaminofluorene (AAF) for either 1 or 2 weeks. For the 2 days prior to the assay, all rats also received 5% cholesterol in the diet. In the control group, the high-cholesterol diet caused almost complete inhibition of cholesterol synthesis, but after AAF treatment the levels of cholesterol synthesis were markedly higher, with considerable variation between individual rats. Uptake of cholesterol- 3 H given p.o. was significantly lower in the AAF group and was also variable, but there was no correlation with sterol synthesis, indicating that impairment of cholesterol uptake is not the critical factor in loss of control. However, liver cholesterol levels in the AAF-fed rats were significantly lower than those in control animals, and there was a highly significant inverse correlation between liver cholesterol levels and sterol synthesis. Therefore, the lack of regulation of cholesterol synthesis induced by AAF appears to be a result of a defect in intracellular storage of cholesterol rather than defective uptake.
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Summary Rat livers were tested for both rate of cholesterol synthesis and uptake of a p.o. dose of cholesterol- 3 H after rats were fed 0.06% 2-acetylaminofluorene (AAF) for either 1 or 2 weeks. For the 2 days prior to the assay, all rats also received 5% cholesterol in the diet. In the control group, the high-cholesterol diet caused almost complete inhibition of cholesterol synthesis, but after AAF treatment the levels of cholesterol synthesis were markedly higher, with considerable variation between individual rats. Uptake of cholesterol- 3 H given p.o. was significantly lower in the AAF group and was also variable, but there was no correlation with sterol synthesis, indicating that impairment of cholesterol uptake is not the critical factor in loss of control. However, liver cholesterol levels in the AAF-fed rats were significantly lower than those in control animals, and there was a highly significant inverse correlation between liver cholesterol levels and sterol synthesis. Therefore, the lack of regulation of cholesterol synthesis induced by AAF appears to be a result of a defect in intracellular storage of cholesterol rather than defective uptake.
Key concepts: Cholesterol, Sterol, 2-Acetylaminofluorene, Internal medicine, Endocrinology, Cholesterol synthesis, Oxysterol, Chemistry