Inhibition of ileal Na+/bile acid cotransporter by S-8921 reduces serum cholesterol and prevents atherosclerosis in rabbits
| Autor: | Takuji Mizui, Tsutomu Shike, Junko Higaki, Seijiro Hara, Kenji Miyata, Nobuo Takasu, Kiyoshi Nagata, Kanya Tonda |
|---|---|
| Rok vydání: | 1998 |
| Předmět: |
Male
medicine.medical_specialty Heterozygote medicine.drug_class Arteriosclerosis Coenzyme A Ileum Naphthols Reductase Biology Bile Acids and Salts Cholesterol Dietary chemistry.chemical_compound Feces Internal medicine medicine Animals Enterohepatic circulation Aorta Lagomorpha Ion Transport Bile acid Cholesterol Anticholesteremic Agents Sodium biology.organism_classification Lipids medicine.anatomical_structure Endocrinology chemistry Liver Depression Chemical LDL receptor Rabbits Cardiology and Cardiovascular Medicine |
| Zdroj: | Arteriosclerosis, thrombosis, and vascular biology. 18(8) |
| ISSN: | 1079-5642 |
| Popis: | Abstract —The ileal Na + /bile acid cotransporter (IBAT) plays an important role in the enterohepatic circulation of bile acids. We investigated the effects of IBAT inhibition on the maintenance of serum cholesterol level by using a novel IBAT inhibitor, S-8921, in rabbits. Administration of S-8921 by its incorporation into the diet (0.01% to 0.1%) for 1 to 2 weeks in heterozygous Watanabe heritable hyperlipidemic rabbits decreased serum cholesterol by 29% to 37% and increased fecal excretion of measured bile acids by 60% to 180% compared with control rabbits. Liver microsomal cholesterol 7α-hydroxylase and 3-hydroxy-3-methylglutaryl coenzyme A reductase activities were increased by 75% to 84% and 84% to 89%, respectively, with S-8921 treatment. S-8921 administration (0.1% in the diet) to normal New Zealand White rabbits for 2 weeks resulted in increased hepatic low density lipoprotein receptor expression, which was assessed by Northern blot analysis. In cholesterol-fed New Zealand White rabbits, S-8921 treatment (0.003% to 0.1% in the diet) for 10 weeks dose-dependently inhibited the development of hypercholesterolemia. It also inhibited the accumulation of cholesterol in the aortic arch and reduced the severity of coronary atherosclerosis. These results indicate that IBAT inhibition by S-8921 affects serum cholesterol, liver enzymes, low density lipoprotein receptor activity, and atherosclerosis in the same manner as bile acid sequestrants. We suggest that an IBAT inhibitor such as S-8921 could be useful in the treatment of hypercholesterolemia. |
| Databáze: | OpenAIRE |
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