Uptake and metabolism of circulating chylomicron triglyceride by rabbit aorta

To determine if chylomicron triglycerides are taken up and metabolized by the arterial wall, rabbit abdominal aortas were perfused in situ for various times up to 2 hr with blood–buffer containing isotopically labeled substrates. Labeled chylomicrons were obtained by feeding [3H]palmitic acid or [3H...

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Main Author: Alan Vost
Format: Article
Language:English
Published: Elsevier 1972-11-01
Series:Journal of Lipid Research
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S0022227520393391
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spelling doaj-b3526d42357d41e68af94e0bf4dbbd5f2021-04-24T05:51:21ZengElsevierJournal of Lipid Research0022-22751972-11-01136695704Uptake and metabolism of circulating chylomicron triglyceride by rabbit aortaAlan Vost0McGill University Medical Clinic, The Montreal General Hospital, Montreal 109, CanadaTo determine if chylomicron triglycerides are taken up and metabolized by the arterial wall, rabbit abdominal aortas were perfused in situ for various times up to 2 hr with blood–buffer containing isotopically labeled substrates. Labeled chylomicrons were obtained by feeding [3H]palmitic acid or [3H]glyceryl trioleate to rats and rabbits with cannulated thoracic ducts. After aortic perfusion with these chylomicrons, more than 85% of aortic lipid ester radioactivity was in triglyceride; when labeled glycerol or palmitic acid was perfused, most aortic ester lipid radioactivity was in diglycerides and phospholipids. This indicated that, during perfusion with chylomicrons, intact triglyceride molecules were taken up by aorta. The rate of triglyceride fatty acid uptake by the inner avascular segment approached maximal values at low concentrations of perfusate triglyceride fatty acids (2 mm), whereas uptake in the outer capillary perfused segment increased with increasing triglyceride fatty acid concentration (0.4–25 mm). By double-radioisotope techniques it was shown that aortic free fatty acid was derived from both perfusate free fatty acids and from hydrolysis of lipoprotein glycerides within the aortic wall. Uptake of chylomicron triglyceride by perfused aorta was independent of triglyceride hydrolysis, which was quantitatively small.http://www.sciencedirect.com/science/article/pii/S0022227520393391perfusiontriglyceridelipolysis
collection DOAJ
language English
format Article
sources DOAJ
author Alan Vost
spellingShingle Alan Vost
Uptake and metabolism of circulating chylomicron triglyceride by rabbit aorta
Journal of Lipid Research
perfusion
triglyceride
lipolysis
author_facet Alan Vost
author_sort Alan Vost
title Uptake and metabolism of circulating chylomicron triglyceride by rabbit aorta
title_short Uptake and metabolism of circulating chylomicron triglyceride by rabbit aorta
title_full Uptake and metabolism of circulating chylomicron triglyceride by rabbit aorta
title_fullStr Uptake and metabolism of circulating chylomicron triglyceride by rabbit aorta
title_full_unstemmed Uptake and metabolism of circulating chylomicron triglyceride by rabbit aorta
title_sort uptake and metabolism of circulating chylomicron triglyceride by rabbit aorta
publisher Elsevier
series Journal of Lipid Research
issn 0022-2275
publishDate 1972-11-01
description To determine if chylomicron triglycerides are taken up and metabolized by the arterial wall, rabbit abdominal aortas were perfused in situ for various times up to 2 hr with blood–buffer containing isotopically labeled substrates. Labeled chylomicrons were obtained by feeding [3H]palmitic acid or [3H]glyceryl trioleate to rats and rabbits with cannulated thoracic ducts. After aortic perfusion with these chylomicrons, more than 85% of aortic lipid ester radioactivity was in triglyceride; when labeled glycerol or palmitic acid was perfused, most aortic ester lipid radioactivity was in diglycerides and phospholipids. This indicated that, during perfusion with chylomicrons, intact triglyceride molecules were taken up by aorta. The rate of triglyceride fatty acid uptake by the inner avascular segment approached maximal values at low concentrations of perfusate triglyceride fatty acids (2 mm), whereas uptake in the outer capillary perfused segment increased with increasing triglyceride fatty acid concentration (0.4–25 mm). By double-radioisotope techniques it was shown that aortic free fatty acid was derived from both perfusate free fatty acids and from hydrolysis of lipoprotein glycerides within the aortic wall. Uptake of chylomicron triglyceride by perfused aorta was independent of triglyceride hydrolysis, which was quantitatively small.
topic perfusion
triglyceride
lipolysis
url http://www.sciencedirect.com/science/article/pii/S0022227520393391
work_keys_str_mv AT alanvost uptakeandmetabolismofcirculatingchylomicrontriglyceridebyrabbitaorta
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