Lipoprotein lipase and hepatic lipase

HDL subspecies Lp(A-I) and Lp(A-I,A-II) have different anti-atherogenic potentials. To determine the role of lipoprotein lipase (LPL) and hepatic lipase (HL) in regulating these particles, we measured these enzyme activities in 28 healthy subjects with well-controlled Type 1 diabetes, and studied th...

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Main Authors: Marian C. Cheung, Shalamar D. Sibley, Jerry P. Palmer, John F. Oram, John D. Brunzell
Format: Article
Language:English
Published: Elsevier 2003-08-01
Series:Journal of Lipid Research
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S0022227520337652
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author Marian C. Cheung
Shalamar D. Sibley
Jerry P. Palmer
John F. Oram
John D. Brunzell
author_facet Marian C. Cheung
Shalamar D. Sibley
Jerry P. Palmer
John F. Oram
John D. Brunzell
author_sort Marian C. Cheung
collection DOAJ
description HDL subspecies Lp(A-I) and Lp(A-I,A-II) have different anti-atherogenic potentials. To determine the role of lipoprotein lipase (LPL) and hepatic lipase (HL) in regulating these particles, we measured these enzyme activities in 28 healthy subjects with well-controlled Type 1 diabetes, and studied their relationship with Lp(A-I) and Lp(A-I,A-II). LPL was positively correlated with the apolipoprotein A-I (apoA-I), cholesterol, and phospholipid mass in total Lp(A-I), and with the apoA-I in large Lp(A-I) (r ≥ 0.58, P ≥ 0.001). HL was negatively correlated with all the above Lp(A-I) parameters plus Lp(A-I) triglyceride (r ≥ −0.53, P ≤ 0.003). No correlation was detected between LPL and Lp(A-I,A-II). However, HL was inversely correlated with total Lp(A-I,A-II) phospholipid, and with large Lp(A-I,A-II) (r ≥ 0.50, P ≤ 0.006). Similar studies were performed with phospholipid transfer protein (PLTP). Only total Lp(A-I) triglyceride in women (not men) (r = 0.71, P = 0.009) was significantly correlated with PLTP activity. These observations indicate that LPL and HL play major roles in determining the level and composition of plasma Lp(A-I), particularly large Lp(A-I), but not with Lp(A-I,A-II) level.Furthermore, select correlations of LPL and/or HL with the apoA-I, cholesterol, and triglyceride of Lp(A-I) but not Lp(A-I,A-II) imply that the apoA-I and lipid of Lp(A-I) and Lp(A-I,A-II) are not fully equilibrated.
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spelling doaj.art-de9988d67e3e4da8b65da98b9df8927a2022-12-21T21:30:19ZengElsevierJournal of Lipid Research0022-22752003-08-0144815521558Lipoprotein lipase and hepatic lipaseMarian C. Cheung0Shalamar D. Sibley1Jerry P. Palmer2John F. Oram3John D. Brunzell4Division of Metabolism, Endocrinology, and Nutrition, Department of Medicine, University of Washington, Seattle, WA 98103; Veterans Administration, Puget Sound Health Care System, Seattle, WA 98108Division of Metabolism, Endocrinology, and Nutrition, Department of Medicine, University of Washington, Seattle, WA 98103; Veterans Administration, Puget Sound Health Care System, Seattle, WA 98108Division of Metabolism, Endocrinology, and Nutrition, Department of Medicine, University of Washington, Seattle, WA 98103; Veterans Administration, Puget Sound Health Care System, Seattle, WA 98108Division of Metabolism, Endocrinology, and Nutrition, Department of Medicine, University of Washington, Seattle, WA 98103; Veterans Administration, Puget Sound Health Care System, Seattle, WA 98108Division of Metabolism, Endocrinology, and Nutrition, Department of Medicine, University of Washington, Seattle, WA 98103; Veterans Administration, Puget Sound Health Care System, Seattle, WA 98108HDL subspecies Lp(A-I) and Lp(A-I,A-II) have different anti-atherogenic potentials. To determine the role of lipoprotein lipase (LPL) and hepatic lipase (HL) in regulating these particles, we measured these enzyme activities in 28 healthy subjects with well-controlled Type 1 diabetes, and studied their relationship with Lp(A-I) and Lp(A-I,A-II). LPL was positively correlated with the apolipoprotein A-I (apoA-I), cholesterol, and phospholipid mass in total Lp(A-I), and with the apoA-I in large Lp(A-I) (r ≥ 0.58, P ≥ 0.001). HL was negatively correlated with all the above Lp(A-I) parameters plus Lp(A-I) triglyceride (r ≥ −0.53, P ≤ 0.003). No correlation was detected between LPL and Lp(A-I,A-II). However, HL was inversely correlated with total Lp(A-I,A-II) phospholipid, and with large Lp(A-I,A-II) (r ≥ 0.50, P ≤ 0.006). Similar studies were performed with phospholipid transfer protein (PLTP). Only total Lp(A-I) triglyceride in women (not men) (r = 0.71, P = 0.009) was significantly correlated with PLTP activity. These observations indicate that LPL and HL play major roles in determining the level and composition of plasma Lp(A-I), particularly large Lp(A-I), but not with Lp(A-I,A-II) level.Furthermore, select correlations of LPL and/or HL with the apoA-I, cholesterol, and triglyceride of Lp(A-I) but not Lp(A-I,A-II) imply that the apoA-I and lipid of Lp(A-I) and Lp(A-I,A-II) are not fully equilibrated.http://www.sciencedirect.com/science/article/pii/S0022227520337652phospholipid transfer proteinhigh density lipoprotein size profileType 1 diabetes
spellingShingle Marian C. Cheung
Shalamar D. Sibley
Jerry P. Palmer
John F. Oram
John D. Brunzell
Lipoprotein lipase and hepatic lipase
Journal of Lipid Research
phospholipid transfer protein
high density lipoprotein size profile
Type 1 diabetes
title Lipoprotein lipase and hepatic lipase
title_full Lipoprotein lipase and hepatic lipase
title_fullStr Lipoprotein lipase and hepatic lipase
title_full_unstemmed Lipoprotein lipase and hepatic lipase
title_short Lipoprotein lipase and hepatic lipase
title_sort lipoprotein lipase and hepatic lipase
topic phospholipid transfer protein
high density lipoprotein size profile
Type 1 diabetes
url http://www.sciencedirect.com/science/article/pii/S0022227520337652
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AT johndbrunzell lipoproteinlipaseandhepaticlipase