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Subcutaneous Adipocyte Lipolysis Contributes to Circulating Lipid Levels

OBJECTIVE—: Fatty acids released via fat cell lipolysis can affect circulating lipid levels. However, the contribution of different lipolysis measures in adipose tissue is unknown and was presently examined in isolated subcutaneous adipocytes. APPROACH AND RESULTS—: One thousand and sixty-six men an...

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Autores principales: Rydén, Mikael, Arner, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5567402/
https://www.ncbi.nlm.nih.gov/pubmed/28663255
http://dx.doi.org/10.1161/ATVBAHA.117.309759
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author Rydén, Mikael
Arner, Peter
author_facet Rydén, Mikael
Arner, Peter
author_sort Rydén, Mikael
collection PubMed
description OBJECTIVE—: Fatty acids released via fat cell lipolysis can affect circulating lipid levels. However, the contribution of different lipolysis measures in adipose tissue is unknown and was presently examined in isolated subcutaneous adipocytes. APPROACH AND RESULTS—: One thousand and sixty-six men and women were examined for lipolysis regulation in subcutaneous abdominal fat cells. Results were compared with fasting plasma levels of total cholesterol, high-density lipoprotein (HDL) cholesterol (HDL-C) and triglycerides. Spontaneous (basal) lipolysis and the effects of the major hormones stimulating (catecholamines and natriuretic peptides) and inhibiting lipolysis (insulin) were examined. Several statistically significant (P<0.0001) correlations between the different lipolysis parameters and plasma lipids were observed. However, physiologically relevant correlations (adjusted r(2)≥0.05) were only evident between basal or insulin-inhibited lipolysis and plasma triglycerides or HDL-C. Together, these lipolysis measures explained 14% of the variation in triglycerides or HDL-C, respectively. In comparison, a combination of established factors associated with variations in plasma lipids, that is, age; body mass index; waist circumference; waist-to-hip ratio; sex; nicotine use; fat cell volume; and pharmacotherapy against diabetes mellitus; hypertension; or hyperlipidemia explained 17% and 28%, respectively, of the variations in plasma triglycerides and HDL-C. CONCLUSIONS—: Subcutaneous fat cell lipolysis is an important independent contributor to interindividual variations in plasma lipids. High spontaneous lipolysis activity and resistance to the antilipolytic effect of insulin associate with elevated triglyceride and low HDL-C concentrations. Thus, although several other factors also play a role, subcutaneous adipose tissue may have a causal influence on dyslipidemia.
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spelling pubmed-55674022017-09-05 Subcutaneous Adipocyte Lipolysis Contributes to Circulating Lipid Levels Rydén, Mikael Arner, Peter Arterioscler Thromb Vasc Biol Clinical and Population Studies OBJECTIVE—: Fatty acids released via fat cell lipolysis can affect circulating lipid levels. However, the contribution of different lipolysis measures in adipose tissue is unknown and was presently examined in isolated subcutaneous adipocytes. APPROACH AND RESULTS—: One thousand and sixty-six men and women were examined for lipolysis regulation in subcutaneous abdominal fat cells. Results were compared with fasting plasma levels of total cholesterol, high-density lipoprotein (HDL) cholesterol (HDL-C) and triglycerides. Spontaneous (basal) lipolysis and the effects of the major hormones stimulating (catecholamines and natriuretic peptides) and inhibiting lipolysis (insulin) were examined. Several statistically significant (P<0.0001) correlations between the different lipolysis parameters and plasma lipids were observed. However, physiologically relevant correlations (adjusted r(2)≥0.05) were only evident between basal or insulin-inhibited lipolysis and plasma triglycerides or HDL-C. Together, these lipolysis measures explained 14% of the variation in triglycerides or HDL-C, respectively. In comparison, a combination of established factors associated with variations in plasma lipids, that is, age; body mass index; waist circumference; waist-to-hip ratio; sex; nicotine use; fat cell volume; and pharmacotherapy against diabetes mellitus; hypertension; or hyperlipidemia explained 17% and 28%, respectively, of the variations in plasma triglycerides and HDL-C. CONCLUSIONS—: Subcutaneous fat cell lipolysis is an important independent contributor to interindividual variations in plasma lipids. High spontaneous lipolysis activity and resistance to the antilipolytic effect of insulin associate with elevated triglyceride and low HDL-C concentrations. Thus, although several other factors also play a role, subcutaneous adipose tissue may have a causal influence on dyslipidemia. Lippincott Williams & Wilkins 2017-09 2017-08-23 /pmc/articles/PMC5567402/ /pubmed/28663255 http://dx.doi.org/10.1161/ATVBAHA.117.309759 Text en © 2017 The Authors. Arteriosclerosis, Thrombosis, and Vascular Biology is published on behalf of the American Heart Association, Inc., by Wolters Kluwer Health, Inc. This is an open access article under the terms of the Creative Commons Attribution Non-Commercial-NoDerivs (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use, distribution, and reproduction in any medium, provided that the original work is properly cited, the use is noncommercial, and no modifications or adaptations are made.
spellingShingle Clinical and Population Studies
Rydén, Mikael
Arner, Peter
Subcutaneous Adipocyte Lipolysis Contributes to Circulating Lipid Levels
title Subcutaneous Adipocyte Lipolysis Contributes to Circulating Lipid Levels
title_full Subcutaneous Adipocyte Lipolysis Contributes to Circulating Lipid Levels
title_fullStr Subcutaneous Adipocyte Lipolysis Contributes to Circulating Lipid Levels
title_full_unstemmed Subcutaneous Adipocyte Lipolysis Contributes to Circulating Lipid Levels
title_short Subcutaneous Adipocyte Lipolysis Contributes to Circulating Lipid Levels
title_sort subcutaneous adipocyte lipolysis contributes to circulating lipid levels
topic Clinical and Population Studies
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5567402/
https://www.ncbi.nlm.nih.gov/pubmed/28663255
http://dx.doi.org/10.1161/ATVBAHA.117.309759
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