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Influence of Duration of Cholesterol Feeding on Esterification of Fatty Acids by Cell-Free Preparation of Pigeon Aorta

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TLDR
Influence of duration of cholesterol feeding on esterification of fatty acids and hydrolysis of cholesteryl esters was studied in cell-free preparations of aorta from White Carneau pigeons, a mechanism similar to that described for liver and adrenal cortex.
Abstract
Influence of duration of cholesterol feeding on esterification of fatty acids and hydrolysis of cholesteryl esters was studied in cell-free preparations of aorta from White Carneau pigeons. Esterification of fatty acids required ATP and CoA; greater than 80% of the esterifying activity was located in the particulate fraction obtained by centrifugation at 105,000x g (after a preliminary centrifugation at 1000x g ). Fatty acids were incorporated most efficiently into phospholipid, primarily (82%) lecithin. Greater than 87% of the fatty acid was esterified at the 2-position. During 8 months of cholesterol feeding, incorporation of oleic acid into phospholipids and triglycerides increased relatively little (less than double that of controls); no changes were seen before 1 month. Esterification of oleic acid to cholesterol was increased after 2 weeks of cholesterol feeding (before gross lesions were seen), eventually reaching a maximum increase of 30- to 50-fold. Cholesterol was esterified by transfer of fatty acyl-CoA to cholesterol, a mechanism similar to that described for liver and adrenal cortex. Little if any cholesterol esterification occurred when lecithin labeled at the 2-position with oleic acid-l-14C was used as substrate. The relationship between duration of cholesterol feeding and hydrolysis of cholesteryl oleate could not be evaluated since results depend directly on an unknown extent of equilibration of substrate with pre-existing cholesteryl ester pools.

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Book ChapterDOI

The relationship between plasma and tissue lipids in human atherosclerosis.

TL;DR: This chapter discusses the relationship between plasma and tissue lipids in human atherosclerosis with a marked increase in the proportion of free cholesterol, decrease in proportion of ester cholesterol, and change in the cholesterol ester fatty acid pattern in normal intima.
Journal ArticleDOI

CL 277,082: a novel inhibitor of ACAT-catalyzed cholesterol esterification and cholesterol absorption

TL;DR: CL 277,082 (I) was a potent inhibitor of cholesterol absorption in cholesterol-fed rats by markedly inhibiting increases in liver and serum cholesterol concentration while increasing the excretion of neutral 14C-labeled sterol in the feces.
Journal ArticleDOI

Regulation of acyl-CoA:cholesterol acyltransferase activity in normal and atherosclerotic rabbit aortas: role of a cholesterol substrate pool.

TL;DR: It was found that hypercholesterolemia results in the expansion of the cholesterol substrate pool of ACAT, and a 21-fold increase in ACAT activity in atherosclerotic aortas observed in this study.
References
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Journal Article

Protein Measurement with the Folin Phenol Reagent

TL;DR: Procedures are described for measuring protein in solution or after precipitation with acids or other agents, and for the determination of as little as 0.2 gamma of protein.
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A simple method for the isolation and purification of total lipides from animal tissues.

TL;DR: In this paper, the authors described a simplified version of the method and reported the results of a study of its application to different tissues, including the efficiency of the washing procedure in terms of the removal from tissue lipides of some non-lipide substances of special biochemical interest.
Journal ArticleDOI

The formation of cholesterol esters with rat liver enzymes.

TL;DR: Experiments dealing with the formation of long chain fatty acid esters of cholesterol with rat liver preparations found that the bulk of hydrolytic enzyme activity is present in the soluble fraction of the liver homogenate.
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