Ezetimibe potently inhibits cholesterol absorption but does not affect acute hepatic or intestinal cholesterol synthesis in rats
| Autor: | Douglas S Compton, Harry R. Davis, Lizbeth M. Hoos, April Smith-Torhan, Margaret van Heek, Constance Farley |
|---|---|
| Rok vydání: | 2003 |
| Předmět: |
Pharmacology
medicine.medical_specialty biology medicine.drug_class Cholesterol Reverse cholesterol transport chemistry.chemical_compound Endocrinology chemistry Ezetimibe Internal medicine HMG-CoA reductase biology.protein Cholesteryl ester medicine Intestinal cholesterol absorption lipids (amino acids peptides and proteins) Cholesterol absorption inhibitor Ketoconazole medicine.drug |
| Zdroj: | British Journal of Pharmacology. 138:1459-1464 |
| ISSN: | 0007-1188 |
| Popis: | Ezetimibe (1-(4-fluorophenyl)-(3R)-[3-(4-fluorophenyl)-(3S)-hydroxypropyl]-(4S)-(4-hydroxyphenyl)-2-azetidinone) and its analog SCH48461 are potent and selective cholesterol absorption inhibitors that inhibit the transport of cholesterol across the intestinal wall, thereby lowering plasma cholesterol. After a dose response for ezetimibe in rats was established, experiments were conducted to determine whether acute administration could alter hepatic or intestinal cholesterol synthesis. To determine whether this class of intestinal cholesterol absorption inhibitors could discriminate between newly synthesized cholesterol in the intestine versus exogenously administered cholesterol, rats were intraduodenally dosed with 14C-cholesterol and 3H-mevalonate, and mesenteric lymph was analyzed for radiolabeled cholesterol and cholesteryl ester content. Ezetimibe attenuated diet-induced hypercholesterolemia 60–94% at doses of 0.1–3 mg kg−1 in rats. A single administration of ezetimibe did not have a direct effect on intestinal or hepatic cholesterol synthesis, while ketoconazole significantly inhibited cholesterol synthesis after a single dose. The ezetimibe analog, SCH48461, inhibited the movement of exogenously administered cholesterol into lymph, but did not affect the appearance of newly synthesized cholesterol into lymph. These data suggest that this class of cholesterol absorption inhibitors does discriminate by blocking the movement of exogenous cholesterol in the enterocyte before it reaches the intracellular cholesterol pool to be incorporated into intestinal lipoproteins, without affecting the incorporation of newly synthesized cholesterol into intestinal lipoproteins. British Journal of Pharmacology (2003) 138, 1459–1464. doi:10.1038/sj.bjp.0705187 |
| Databáze: | OpenAIRE |
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