Metabolic patterns and insulin responsiveness of enlarging fat cells

The rate and pattern of glucose metabolism, basal lipolysis, and intracellular concentration of free fatty acids were determined in isolated epididymal fat cell preparations (mean volume 30-800 pl) from rats on the basis of fat cell number and in relation to the cell volume. The effects of increasin...

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Main Authors: Mario DiGirolamo, Mary D. Howe, John Esposito, Lynda Thurman, Jeanna L. Owens
Format: Article
Language:English
Published: Elsevier 1974-07-01
Series:Journal of Lipid Research
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S0022227520367808
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author Mario DiGirolamo
Mary D. Howe
John Esposito
Lynda Thurman
Jeanna L. Owens
author_facet Mario DiGirolamo
Mary D. Howe
John Esposito
Lynda Thurman
Jeanna L. Owens
author_sort Mario DiGirolamo
collection DOAJ
description The rate and pattern of glucose metabolism, basal lipolysis, and intracellular concentration of free fatty acids were determined in isolated epididymal fat cell preparations (mean volume 30-800 pl) from rats on the basis of fat cell number and in relation to the cell volume. The effects of increasing glucose concentrations in the medium and of insulin on the cellular metabolic activities were compared. Expanding fat cell volume correlated positively and significantly (P < 0.001) with the synthesis of glyceride glycerol from glucose (correlation coefficient, r = 0.919), with rates of basal lipolysis (r = 0.663), and with intracellular free fatty acid accumulation (r = 0.796); it correlated negatively and significantly with glucose conversion to glyceride fatty acids (r = -0.814, P < 0.01). The differences in patterns of glucose metabolism and basal lipolysis between small (<100 pl) and large (>400 pl) fat cells were not modified by insulin or by increments in glucose concentration. The results indicate that the reduced capacity of the large fat cells to respond to insulin cannot be attributed solely to a limited capacity of the cells to take up and metabolize increasing amounts of glucose. The acquired unresponsiveness of the large cells to insulin may result from an alteration in the mechanism of action of insulin and may be related to an intracellular metabolic derangement with increased basal lipolysis, free fatty acid accumulation, and accelerated glyceride synthesis resulting from the accumulation of triglyceride.
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spelling doaj.art-7894679cae514d618a7986161d68439f2022-12-21T19:48:51ZengElsevierJournal of Lipid Research0022-22751974-07-01154332338Metabolic patterns and insulin responsiveness of enlarging fat cellsMario DiGirolamo0Mary D. Howe1John Esposito2Lynda Thurman3Jeanna L. Owens4Division of Endocrinology, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia 30303Division of Endocrinology, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia 30303Division of Endocrinology, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia 30303Division of Endocrinology, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia 30303Division of Endocrinology, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia 30303The rate and pattern of glucose metabolism, basal lipolysis, and intracellular concentration of free fatty acids were determined in isolated epididymal fat cell preparations (mean volume 30-800 pl) from rats on the basis of fat cell number and in relation to the cell volume. The effects of increasing glucose concentrations in the medium and of insulin on the cellular metabolic activities were compared. Expanding fat cell volume correlated positively and significantly (P < 0.001) with the synthesis of glyceride glycerol from glucose (correlation coefficient, r = 0.919), with rates of basal lipolysis (r = 0.663), and with intracellular free fatty acid accumulation (r = 0.796); it correlated negatively and significantly with glucose conversion to glyceride fatty acids (r = -0.814, P < 0.01). The differences in patterns of glucose metabolism and basal lipolysis between small (<100 pl) and large (>400 pl) fat cells were not modified by insulin or by increments in glucose concentration. The results indicate that the reduced capacity of the large fat cells to respond to insulin cannot be attributed solely to a limited capacity of the cells to take up and metabolize increasing amounts of glucose. The acquired unresponsiveness of the large cells to insulin may result from an alteration in the mechanism of action of insulin and may be related to an intracellular metabolic derangement with increased basal lipolysis, free fatty acid accumulation, and accelerated glyceride synthesis resulting from the accumulation of triglyceride.http://www.sciencedirect.com/science/article/pii/S0022227520367808glucose metabolismlipolysisfat cell sizelipogenesisglyceride glycerol synthesisintracellular free fatty acids
spellingShingle Mario DiGirolamo
Mary D. Howe
John Esposito
Lynda Thurman
Jeanna L. Owens
Metabolic patterns and insulin responsiveness of enlarging fat cells
Journal of Lipid Research
glucose metabolism
lipolysis
fat cell size
lipogenesis
glyceride glycerol synthesis
intracellular free fatty acids
title Metabolic patterns and insulin responsiveness of enlarging fat cells
title_full Metabolic patterns and insulin responsiveness of enlarging fat cells
title_fullStr Metabolic patterns and insulin responsiveness of enlarging fat cells
title_full_unstemmed Metabolic patterns and insulin responsiveness of enlarging fat cells
title_short Metabolic patterns and insulin responsiveness of enlarging fat cells
title_sort metabolic patterns and insulin responsiveness of enlarging fat cells
topic glucose metabolism
lipolysis
fat cell size
lipogenesis
glyceride glycerol synthesis
intracellular free fatty acids
url http://www.sciencedirect.com/science/article/pii/S0022227520367808
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AT johnesposito metabolicpatternsandinsulinresponsivenessofenlargingfatcells
AT lyndathurman metabolicpatternsandinsulinresponsivenessofenlargingfatcells
AT jeannalowens metabolicpatternsandinsulinresponsivenessofenlargingfatcells