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Research Article Free access | 10.1172/JCI115397

Dietary fish oil-induced changes in intrahepatic cholesterol transport and bile acid synthesis in rats.

M J Smit, A M Temmerman, H Wolters, F Kuipers, A C Beynen, and R J Vonk

Department of Pediatrics, University of Groningen, The Netherlands.

Find articles by Smit, M. in: PubMed | Google Scholar

Department of Pediatrics, University of Groningen, The Netherlands.

Find articles by Temmerman, A. in: PubMed | Google Scholar

Department of Pediatrics, University of Groningen, The Netherlands.

Find articles by Wolters, H. in: PubMed | Google Scholar

Department of Pediatrics, University of Groningen, The Netherlands.

Find articles by Kuipers, F. in: PubMed | Google Scholar

Department of Pediatrics, University of Groningen, The Netherlands.

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Department of Pediatrics, University of Groningen, The Netherlands.

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Published September 1, 1991 - More info

Published in Volume 88, Issue 3 on September 1, 1991
J Clin Invest. 1991;88(3):943–951. https://doi.org/10.1172/JCI115397.
© 1991 The American Society for Clinical Investigation
Published September 1, 1991 - Version history
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Abstract

Hepatic cholesterol metabolism was studied in rats fed purified diets supplemented (9% wt/wt) with either fish oil (FO) (n-3 fatty acids) or corn oil (CO) (n-6 fatty acids) for 4 wk. Rats were equipped with permanent catheters in heart, bile duct, and duodenum to allow studies under normal feeding conditions. [3H]-cholesteryl oleate-labeled small unilamellar liposomes, which are rapidly endocytosed by hepatocytes, were intravenously injected to label intrahepatic cholesterol pools, and plasma and bile were collected. FO as compared to CO induced a lowering of plasma cholesterol levels by 38% and of triglyceride levels by 69%. This reduction in plasma lipids in FO rats was accompanied by: (a) an increased bile acid pool size (28%); (b) a fourfold increase in the ratio cholic acid/chenodeoxycholic acid in bile; (c) increased biliary excretion of cholesterol (51%); (d) accelerated excretion of endocytosed free cholesterol into bile; (e) accelerated incorporation of endocytosed cholesterol in bile acids; (f) a significant increase in the bile acid-independent fraction of bile flow; and (g) a threefold increase in hepatic alkaline phosphatase activity. The results show that FO induces changes in transport and metabolic pathways of cholesterol in the rat liver, which result in a more rapid disposition of plasma-derived cholesterol into the bile.

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