Document Detail


The role of different albumin preparations on production of human plasma lipoprotein-like particles in vitro.
MedLine Citation:
PMID:  7381334     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Because we found apoprotein contamination of some high-grade commercial albumins, we studied this effect on formation of lipoprotein-like particles during lipolysis of human very low density lipoprotein (VLDL) in vitro. After a 1-hr incubation with purified bovine milk lipoprotein lipase, over 98% VLDL triglyceride was hydrolyzed in the presence of either albumin B (apoprotein-rich) or albumin C (apoprotein-poor), with a weight ratio of albumin to triglyceride of 60 to 1. Lipoproteins of density < 1.019 g/ml ("IDL"), 1.019 to 1.063 g/ml ("LDL"), and 1.063 to 1.21 g/ml ("HDL") were then isolated by ultracentrifugation. Recovery of non-triglyceride VLDL constituents in "IDL" and "LDL" was similar for albumin B or albumin C. "LDL" was the major catabolic product of in vitro VLDL lipolysis independent of the albumin used. The yield of "HDL," however, was 5- to 6-fold greater with albumin B. All lipoproteins produced with albumin B were richer in phospholipid, apoproteins C and A-I, relative to lipoproteins produced in the presence of albumin C. With albumin B, cholesterol/phospholipid molar ratios were <1 in all in vitro produced lipoproteins, but were >1 with albumin C. All these differences can be ascribed to the presence in albumin B of 0.2 mg apoprotein A-I/g albumin and 1.8 mg phospholipid/g albumin; these components were not detected in albumin C. Thus, two thirds of "HDL" recovered with VLDL lipolysis in the presence of albumin B can be accounted for by albumin itself and only one third from constituents of VLDL. Adding equivalent amounts of both apoproteins removed from albumin B and phospholipid to albumin C markedly decreased the disparities in results but addition of each alone did not. These results prove "inert" albumins serve other than as fatty acid and lysolecithin acceptors in in vitro model systems, and do influence formation of lipoproteins during in vitro VLDL catabolism.-Deckelbaum, R. J., T. Olivecrona, and M. Fainaru. The role of different albumin preparations on production of human plasma lipoprotein-like particles in vitro.
Authors:
R J Deckelbaum; T Olivecrona; M Fainaru
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Publication Detail:
Type:  Journal Article; Research Support, U.S. Gov't, Non-P.H.S.    
Journal Detail:
Title:  Journal of lipid research     Volume:  21     ISSN:  0022-2275     ISO Abbreviation:  J. Lipid Res.     Publication Date:  1980 May 
Date Detail:
Created Date:  1980-08-28     Completed Date:  1980-08-28     Revised Date:  2007-03-23    
Medline Journal Info:
Nlm Unique ID:  0376606     Medline TA:  J Lipid Res     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  425-34     Citation Subset:  IM    
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MeSH Terms
Descriptor/Qualifier:
Albumins / pharmacology*,  standards
Apoproteins / metabolism,  pharmacology
Cholesterol / metabolism
Electrophoresis, Polyacrylamide Gel
Humans
Lipolysis / drug effects
Lipoprotein Lipase / metabolism
Lipoproteins / blood*
Lipoproteins, HDL / metabolism
Lipoproteins, LDL / metabolism
Lipoproteins, VLDL / blood
Male
Phospholipids / metabolism
Triglycerides / blood
Ultracentrifugation
Chemical
Reg. No./Substance:
0/Albumins; 0/Apoproteins; 0/Lipoproteins; 0/Lipoproteins, HDL; 0/Lipoproteins, LDL; 0/Lipoproteins, VLDL; 0/Phospholipids; 0/Triglycerides; 57-88-5/Cholesterol; EC 3.1.1.34/Lipoprotein Lipase

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