Effects of F2833 on cholesterol metabolism in the genetically hyperlipidemic rat
Autor: | Thierry Magot, Claude Lutton, Khadija Ouguerram, André Delhon |
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Rok vydání: | 2001 |
Předmět: |
Male
medicine.medical_specialty Hyperlipidemias Stimulation Increased Cholesterol Synthesis Biology chemistry.chemical_compound Internal medicine medicine Animals Cholesterol metabolism Phospholipids Triglycerides Hypolipidemic Agents Pharmacology Catabolism Cholesterol Biphenyl Compounds Biological activity Cholesterol LDL Rats Endocrinology chemistry Mechanism of action lipids (amino acids peptides and proteins) medicine.symptom Lipoprotein |
Zdroj: | European Journal of Pharmacology. 415:293-299 |
ISSN: | 0014-2999 |
DOI: | 10.1016/s0014-2999(01)00820-2 |
Popis: | The effects of the new hypolipidemic agent, F2833 or (chloro 2' (1-1') biphenyl-4)-2 propanol-2, on cholesterol metabolism were studied in genetically hyperlipidemic rats (RICO). Cholesterolemia decreased after 2 days of treatment to 60% of its initial value (1.20+/-0.10 g/l vs. 1.99+/-0.08, P < 0.001) and then stabilised within 10 days. This hypocholesterolemic action was effective for as long as 3 months. Concerning the different classes of lipoproteins, a significant drop was observed in HDL (high density lipoproteins) (25%, 0.49 +/- 0.02 g/l vs. 0.66 +/- 0.007, P < 0.01) and particularly in LDL (low density lipoproteins) (70%, 0.30 +/- 0.04 g/l vs. 0.92 +/- 0.05, P < 0.001). Whole body cholesterol showed a higher fractional catabolic rate (0.25 +/- 0.02 vs. 0.17 +/- 0.005 day(-1), P < 0.01) together with an increased cholesterol synthesis (60 +/- 5 vs. 36 +/- 4 mg/day, P < 0.01). LDL kinetics showed that the decrease in these lipoproteins is essentially caused by an increase in the fractional catabolic rate (10.6 +/-0.1%/h vs. 5.2 +/- 0.1%/h, P < 0.001) and by a lesser decrease in the LDL production rate. This cholesterol metabolic profile created by treatment suggests an effect through stimulation of cholesterol output (biliary cholesterol elimination or cholesterol transformation into bile acids). |
Databáze: | OpenAIRE |
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