J. Lipid Res. Did you know there is a large type edition? Click here.
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Lamarche, B.
Right arrow Articles by Lewis, G. F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Lamarche, B.
Right arrow Articles by Lewis, G. F.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

The Journal of Lipid Research, Vol. 39, 1162-1172, June 1998
Copyright © 1998 by Lipid Research, Inc.


Original Article

Analysis of particle size and lipid composition as determinants of the metabolic clearance of human high density lipoproteins in a rabbit model

Benoît Lamarchea, Kristine D. Uffelmana, George Steinera, P. Hugh R. Barrettb, and Gary F. Lewisa
a Department of Medicine, Division of Endocrinology, University of Toronto, Toronto, Ontario M5G 2C4, Canada and The Resource Facility for Kinetic Analysis,
b Department of Medicine, Department of Bioengineering, Box 352255, University of Washington, Seattle, WA, USA 98195

Correspondence to: Gary F. Lewis.

Hypertriglyceridemia is commonly associated with triglyceride (TG) enrichment of high density lipoprotein (HDL) and reduction in HDL cholesterol and apolipoprotein A-I levels. We have recently reported that lipolytic modification of TG-rich HDL, which reduces particle size, enhances its clearance from the circulation. In the present study, we examined the role of particle size and lipid composition in determining the metabolic clearance of human HDL, in the absence of substantial in vivo modification of the particle by hepatic lipase. The rabbit, which has a very low hepatic lipase activity, was used for this purpose. Plasma fractions d < 1.21 g/ml were first isolated by ultracentrifugation from fasting humans with normal (NTG, n = 6, mean plasma TG concentration = 1.26 ± 0.21 (SEM) mmol/l) or elevated plasma TG levels (HTG, n = 5, TG = 4.49 ± 0.65 mmol/l). Small and large HDL particles were separated by gel filtration chromatography and were labeled with either 125I or 131I. Large HDL were cleared more rapidly than small HDL in 10 out of 11 studies (P = 0.006). There was, however, no difference in the fractional catabolic rate (FCR) of large HDL isolated from NTG versus from HTG subjects or in the FCR of small HDL from NTG versus HTG individuals. There was also no correlation between the TG content of HDL and its FCR. In summary, large, lipid-rich human high density lipoproteins (HDL) are cleared more rapidly than small human HDL in rabbits.

These results, combined with our previous observation, also support the hypothesis that triglyceride enrichment of HDL, in the absence of substantial lipolytic modification, is not sufficient to enhance its clearance from the circulation.—Lamarche, B., K. D. Uffelmann, G. Steiner, P. H. R. Barrett, and G. F. Lewis. Analysis of particle size and lipid composition as determinants of the metabolic clearance of human high density lipoproteins in a rabbit model. J. Lipid Res. 1998. 39: 1162–1172.

Supplementary key words: kinetics, hepatic lipase, metabolism, hypertriglyceridemia, rabbits, radioisotopes


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?


This article has been cited by other articles:


Home page
Circ. Res.Home page
C. Xiao, T. Watanabe, Y. Zhang, B. Trigatti, L. Szeto, P. W. Connelly, S. Marcovina, T. Vaisar, J. W. Heinecke, and G. F. Lewis
Enhanced Cellular Uptake of Remnant High-Density Lipoprotein Particles: A Mechanism for High-Density Lipoprotein Lowering in Insulin Resistance and Hypertriglyceridemia
Circ. Res., July 18, 2008; 103(2): 159 - 166.
[Abstract] [Full Text] [PDF]


Home page
CirculationHome page
S. Rashid, K. D. Uffelman, P. H. R. Barrett, and G. F. Lewis
Effect of Atorvastatin on High-Density Lipoprotein Apolipoprotein A-I Production and Clearance in the New Zealand White Rabbit
Circulation, December 3, 2002; 106(23): 2955 - 2960.
[Abstract] [Full Text] [PDF]


Home page
J. Lipid Res.Home page
J. W. Skeggs and R. E. Morton
LDL and HDL enriched in triglyceride promote abnormal cholesterol transport
J. Lipid Res., August 1, 2002; 43(8): 1264 - 1274.
[Abstract] [Full Text] [PDF]


Home page
Arterioscler. Thromb. Vasc. Bio.Home page
S. Rashid, P. H. R. Barrett, K. D. Uffelman, T. Watanabe, K. Adeli, and G. F. Lewis
Lipolytically Modified Triglyceride-Enriched HDLs Are Rapidly Cleared From the Circulation
Arterioscler. Thromb. Vasc. Biol., March 1, 2002; 22(3): 483 - 487.
[Abstract] [Full Text] [PDF]


Home page
J. Lipid Res.Home page
M. Perusse, A. Pascot, J.-P. Despres, C. Couillard, and B. Lamarche
A new method for HDL particle sizing by polyacrylamide gradient gel electrophoresis using whole plasma
J. Lipid Res., August 1, 2001; 42(8): 1331 - 1334.
[Abstract] [Full Text] [PDF]


Home page
J. Lipid Res.Home page
S. Rashid, K. D. Uffelman, P. H. R. Barrett, P. Vicini, K. Adeli, and G. F. Lewis
Triglyceride enrichment of HDL does not alter HDL-selective cholesteryl ester clearance in rabbits
J. Lipid Res., February 1, 2001; 42(2): 265 - 271.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 All ASBMB Journals   Journal of Biological Chemistry 
 Molecular and Cellular Proteomics   ASBMB Today 
Copyright © 1998 by the American Society for Biochemistry and Molecular Biology.