The nature of the epinephrine-induced hyperlipidemia in dogs and its modification by glucose

Dogs receiving subcutaneous epinephrine in oil (1 mg. per kg.) showed a prompt but transient elevation in serum free fatty acids (FFA) and a delayed %-hour elevation of serum lipoproteins. On daily injections of epinephrine for 6 to 8 days the serum cholesterol rose to 91 per cent above control valu...

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Main Authors: Eleazar Shafrir, Karl E. Sussman, Daniel Steinberg
Format: Article
Language:English
Published: Elsevier 1959-10-01
Series:Journal of Lipid Research
Online Access:http://www.sciencedirect.com/science/article/pii/S002222752039101X
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spelling doaj-c6fbb0d1e31f425cb8670835e6a81a402021-04-23T06:11:12ZengElsevierJournal of Lipid Research0022-22751959-10-0111109117The nature of the epinephrine-induced hyperlipidemia in dogs and its modification by glucoseEleazar Shafrir0Karl E. Sussman1Daniel Steinberg2Section on Metabolism, Laboratory of Cellular Physiology and Metabolism, National Heart Institute, National Institutes of Health, Bethesda 14, MarylandSection on Metabolism, Laboratory of Cellular Physiology and Metabolism, National Heart Institute, National Institutes of Health, Bethesda 14, MarylandSection on Metabolism, Laboratory of Cellular Physiology and Metabolism, National Heart Institute, National Institutes of Health, Bethesda 14, MarylandDogs receiving subcutaneous epinephrine in oil (1 mg. per kg.) showed a prompt but transient elevation in serum free fatty acids (FFA) and a delayed %-hour elevation of serum lipoproteins. On daily injections of epinephrine for 6 to 8 days the serum cholesterol rose to 91 per cent above control values and the phospholipid 53 per cent. The triglyceride response was smaller and quite variable. Little change was found in the d < 1.019 lipoprotein, a three to eightfold increase in the d = 1.019 to 1.063 fraction and a 15 to 41 per cent increase in the d = 1.063 to 121 fraction. Epinephrine prolonged alimentary lipidemia but did not inhibit disappearance of intravenously infused chylomicrons. By prior and concomitant administration of glucose the FFA elevation after epinephrine was prevented. Insulin alone also blocked the epinephrine-induced FFA response without parallel hyperglycemia, indicating that availability of glucose for effective tissue utilization rather than hyperglycemia per se controls the release of FFA. Despite the block in the FFA response to epinephrine by either glucose or insulin, there was a definite elevation of serum cholesterol and phospholipids at 24 hours, suggesting an at least partially independent lipoprotein mobilizing action of the hormone. The relation of these findings to stress-induced hypercholesterolemia is considered.http://www.sciencedirect.com/science/article/pii/S002222752039101X
collection DOAJ
language English
format Article
sources DOAJ
author Eleazar Shafrir
Karl E. Sussman
Daniel Steinberg
spellingShingle Eleazar Shafrir
Karl E. Sussman
Daniel Steinberg
The nature of the epinephrine-induced hyperlipidemia in dogs and its modification by glucose
Journal of Lipid Research
author_facet Eleazar Shafrir
Karl E. Sussman
Daniel Steinberg
author_sort Eleazar Shafrir
title The nature of the epinephrine-induced hyperlipidemia in dogs and its modification by glucose
title_short The nature of the epinephrine-induced hyperlipidemia in dogs and its modification by glucose
title_full The nature of the epinephrine-induced hyperlipidemia in dogs and its modification by glucose
title_fullStr The nature of the epinephrine-induced hyperlipidemia in dogs and its modification by glucose
title_full_unstemmed The nature of the epinephrine-induced hyperlipidemia in dogs and its modification by glucose
title_sort nature of the epinephrine-induced hyperlipidemia in dogs and its modification by glucose
publisher Elsevier
series Journal of Lipid Research
issn 0022-2275
publishDate 1959-10-01
description Dogs receiving subcutaneous epinephrine in oil (1 mg. per kg.) showed a prompt but transient elevation in serum free fatty acids (FFA) and a delayed %-hour elevation of serum lipoproteins. On daily injections of epinephrine for 6 to 8 days the serum cholesterol rose to 91 per cent above control values and the phospholipid 53 per cent. The triglyceride response was smaller and quite variable. Little change was found in the d < 1.019 lipoprotein, a three to eightfold increase in the d = 1.019 to 1.063 fraction and a 15 to 41 per cent increase in the d = 1.063 to 121 fraction. Epinephrine prolonged alimentary lipidemia but did not inhibit disappearance of intravenously infused chylomicrons. By prior and concomitant administration of glucose the FFA elevation after epinephrine was prevented. Insulin alone also blocked the epinephrine-induced FFA response without parallel hyperglycemia, indicating that availability of glucose for effective tissue utilization rather than hyperglycemia per se controls the release of FFA. Despite the block in the FFA response to epinephrine by either glucose or insulin, there was a definite elevation of serum cholesterol and phospholipids at 24 hours, suggesting an at least partially independent lipoprotein mobilizing action of the hormone. The relation of these findings to stress-induced hypercholesterolemia is considered.
url http://www.sciencedirect.com/science/article/pii/S002222752039101X
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