An electron microscopic and functional study of very low density lipoproteins in intestinal lymph

Previous studies with fasting rats showed that the intestine produces endogenous very low density lipoproteins (VLDL) which resemble those in the plasma. Intestinal VLDL also were found to be important in lipid transport during absorption of saturated but not of unsaturated fat. These findings depen...

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Main Authors: Robert K. Ockner, Albert L. Jones
Format: Article
Language:English
Published: Elsevier 1970-07-01
Series:Journal of Lipid Research
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S0022227520429633
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author Robert K. Ockner
Albert L. Jones
author_facet Robert K. Ockner
Albert L. Jones
author_sort Robert K. Ockner
collection DOAJ
description Previous studies with fasting rats showed that the intestine produces endogenous very low density lipoproteins (VLDL) which resemble those in the plasma. Intestinal VLDL also were found to be important in lipid transport during absorption of saturated but not of unsaturated fat. These findings depended upon separations of a chylomicron-rich fraction (Sf > 400) from VLDL (Sf 20-400) by preparative ultracentrifugation methods based on particle flotation rates. The present studies correlate this method with electron microscopic measurement of lipoprotein particle size.Almost all intestinal lymph lipoprotein particles from fasting rats were less than 750 A in diameter, and could not be distinguished morphologically from plasma VLDL. Cholestyramine administration or bile diversion led to decreased lymph lipid output, correlating with marked reduction in VLDL. This supports the concept that lymph VLDL contain endogenous lipid which is reabsorbed from the intestinal lumen.During exogenous fatty acid absorption, lymph lipoprotein particle sizes were significantly smaller after administration of palmitate than after administration of linoleate, a finding consistent with ultracentrifugal evidence of the importance of VLDL in lipid transport during palmitate absorption.These studies fully confirm and extend earlier observations. Together, they show that the intestine is a source of endogenous VLDL in the fasting animal. In addition, significant quantities of exogenous lipid are transported in VLDL during palmitate absorption, whereas with linoleate absorption nearly all lipid is in chylomicrons. These findings indicate that the small intestine plays a role in lipoprotein metabolism which extends beyond the absorption of dietary fat.
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spelling doaj.art-2148c332a71b4afbb89e23223ad62e7a2022-12-21T22:35:52ZengElsevierJournal of Lipid Research0022-22751970-07-01114284292An electron microscopic and functional study of very low density lipoproteins in intestinal lymphRobert K. Ockner0Albert L. Jones1Departments of Medicine and Anatomy, University of California, San Francisco Medical Center, San Francisco, California 94122; Veterans Administration Hospital, San Francisco, California 94121Departments of Medicine and Anatomy, University of California, San Francisco Medical Center, San Francisco, California 94122; Veterans Administration Hospital, San Francisco, California 94121Previous studies with fasting rats showed that the intestine produces endogenous very low density lipoproteins (VLDL) which resemble those in the plasma. Intestinal VLDL also were found to be important in lipid transport during absorption of saturated but not of unsaturated fat. These findings depended upon separations of a chylomicron-rich fraction (Sf > 400) from VLDL (Sf 20-400) by preparative ultracentrifugation methods based on particle flotation rates. The present studies correlate this method with electron microscopic measurement of lipoprotein particle size.Almost all intestinal lymph lipoprotein particles from fasting rats were less than 750 A in diameter, and could not be distinguished morphologically from plasma VLDL. Cholestyramine administration or bile diversion led to decreased lymph lipid output, correlating with marked reduction in VLDL. This supports the concept that lymph VLDL contain endogenous lipid which is reabsorbed from the intestinal lumen.During exogenous fatty acid absorption, lymph lipoprotein particle sizes were significantly smaller after administration of palmitate than after administration of linoleate, a finding consistent with ultracentrifugal evidence of the importance of VLDL in lipid transport during palmitate absorption.These studies fully confirm and extend earlier observations. Together, they show that the intestine is a source of endogenous VLDL in the fasting animal. In addition, significant quantities of exogenous lipid are transported in VLDL during palmitate absorption, whereas with linoleate absorption nearly all lipid is in chylomicrons. These findings indicate that the small intestine plays a role in lipoprotein metabolism which extends beyond the absorption of dietary fat.http://www.sciencedirect.com/science/article/pii/S0022227520429633bile diversioncholesterolcholestyraminechylomicronsintestinal absorptionlinoleic acid
spellingShingle Robert K. Ockner
Albert L. Jones
An electron microscopic and functional study of very low density lipoproteins in intestinal lymph
Journal of Lipid Research
bile diversion
cholesterol
cholestyramine
chylomicrons
intestinal absorption
linoleic acid
title An electron microscopic and functional study of very low density lipoproteins in intestinal lymph
title_full An electron microscopic and functional study of very low density lipoproteins in intestinal lymph
title_fullStr An electron microscopic and functional study of very low density lipoproteins in intestinal lymph
title_full_unstemmed An electron microscopic and functional study of very low density lipoproteins in intestinal lymph
title_short An electron microscopic and functional study of very low density lipoproteins in intestinal lymph
title_sort electron microscopic and functional study of very low density lipoproteins in intestinal lymph
topic bile diversion
cholesterol
cholestyramine
chylomicrons
intestinal absorption
linoleic acid
url http://www.sciencedirect.com/science/article/pii/S0022227520429633
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