linoleic-acid and cholesteryl-oleate

linoleic-acid has been researched along with cholesteryl-oleate* in 3 studies

Trials

1 trial(s) available for linoleic-acid and cholesteryl-oleate

ArticleYear
High-oleic canola oil consumption enriches LDL particle cholesteryl oleate content and reduces LDL proteoglycan binding in humans.
    Atherosclerosis, 2015, Volume: 238, Issue:2

    Oleic acid consumption is considered cardio-protective according to studies conducted examining effects of the Mediterranean diet. However, animal models have shown that oleic acid consumption increases LDL particle cholesteryl oleate content which is associated with increased LDL-proteoglycan binding and atherosclerosis. The objective was to examine effects of varying oleic, linoleic and docosahexaenoic acid consumption on human LDL-proteoglycan binding in a non-random subset of the Canola Oil Multi-center Intervention Trial (COMIT) participants. COMIT employed a randomized, double-blind, five-period, cross-over trial design. Three of the treatment oil diets: 1) a blend of corn/safflower oil (25:75); 2) high oleic canola oil; and 3) DHA-enriched high oleic canola oil were selected for analysis of LDL-proteoglycan binding in 50 participants exhibiting good compliance. LDL particles were isolated from frozen plasma by gel filtration chromatography and LDL cholesteryl esters quantified by mass-spectrometry. LDL-proteoglycan binding was assessed using surface plasmon resonance. LDL particle cholesterol ester fatty acid composition was sensitive to the treatment fatty acid compositions, with the main fatty acids in the treatments increasing in the LDL cholesterol esters. The corn/safflower oil and high-oleic canola oil diets lowered LDL-proteoglycan binding relative to their baseline values (p = 0.0005 and p = 0.0012, respectively). At endpoint, high-oleic canola oil feeding resulted in lower LDL-proteoglycan binding than corn/safflower oil (p = 0.0243) and DHA-enriched high oleic canola oil (p = 0.0249), although high-oleic canola oil had the lowest binding at baseline (p = 0.0344). Our findings suggest that high-oleic canola oil consumption in humans increases cholesteryl oleate percentage in LDL, but in a manner not associated with a rise in LDL-proteoglycan binding.

    Topics: Adult; Canada; Cardiovascular Diseases; Cholesterol Esters; Cholesterol, LDL; Corn Oil; Cross-Over Studies; Diet, Mediterranean; Dietary Fats; Docosahexaenoic Acids; Double-Blind Method; Fatty Acids, Monounsaturated; Female; Humans; Linoleic Acid; Male; Middle Aged; Oleic Acid; Proteoglycans; Rapeseed Oil; Risk Factors; Risk Reduction Behavior; Safflower Oil; Time Factors; United States

2015

Other Studies

2 other study(ies) available for linoleic-acid and cholesteryl-oleate

ArticleYear
Atomistic simulation studies of cholesteryl oleates: model for the core of lipoprotein particles.
    Biophysical journal, 2006, Apr-01, Volume: 90, Issue:7

    We have conducted molecular dynamics simulations to gain insight into the atomic-scale properties of an isotropic system of cholesteryl oleate (CO) molecules. Cholesteryl esters are major constituents of low density lipoprotein particles, the key players in the formation of atherosclerosis, as well as the storage form of cholesterol. Here the aim is to clarify structural and dynamical properties of CO molecules under conditions, which are suggestive of those in the core of low density lipoprotein particles. The simulations in the fluid phase indicate that the system of CO molecules is characterized by an absence of translational order, as expected, while the orientational order between distinct CO molecules is significant at short distances, persisting over a molecular size. As for intramolecular properties, the bonds along the oleate chain are observed to be weakly ordered with respect to the sterol structure, unlike the bonds along the short hydrocarbon chain of cholesterol where the ordering is significant. The orientational distribution of the oleate chain as a whole with respect to the sterol moiety is of broad nature, having a major amount of extended and a less considerable proportion of bended structures. Distinct transient peaks at specific angles also appear. The diffusion of CO molecules is found to be a slow process and characterized by a diffusion coefficient of the order of 2x10(-9) cm2/s. This is considerably slower than diffusion, e.g., in ordered domains of lipid membranes rich in sphingomyelin and cholesterol. Analysis of the rotational diffusion rates and trans-to-gauche transition rates yield results consistent with experiments.

    Topics: Atherosclerosis; Biophysics; Carbon; Carbon Monoxide; Cholesterol; Cholesterol Esters; Diffusion; Humans; Hydrocarbons; Linoleic Acid; Lipoproteins; Lipoproteins, LDL; Magnetic Resonance Spectroscopy; Models, Chemical; Models, Molecular; Models, Statistical; Models, Theoretical; Neutrons; Protein Conformation; Software; Sterols; Time Factors; X-Ray Diffraction

2006
The effect of lipids on the adherence of axillary aerobic coryneform bacteria.
    Letters in applied microbiology, 2004, Volume: 38, Issue:6

    A wide range of lipids are present on the skin surface of human beings and bacterial lipases are known to modify them. The microflora of the underarm (axilla) is often dominated by aerobic coryneforms and whilst many require lipids for growth, they appear not to be utilized as carbon sources. The aim of this study was to investigate the adherence aerobic coryneforms to lipids present on the skin surface of the human axilla to determine whether they contribute to colonization of the skin.. Aerobic coryneforms were grown in a defined synthetic medium in the presence of (14)C-glucose to produce radio-labelled cells. Adherence to lipids was tested using a thin layer chromatography plate-based assay.. The mechanism of bacterial adhesion to skin lipids is unknown. The results of this study show that a significant proportion of cutaneous aerobic coryneform isolates from the axilla interact with skin lipids resulting in increased adherence, which may contribute to skin colonization.

    Topics: Actinomycetales; Axilla; Bacteria, Aerobic; Bacterial Adhesion; Carbon Isotopes; Cholesterol; Cholesterol Esters; Diglycerides; Glycerides; Linoleic Acid; Lipid Metabolism; Oleic Acid; Skin; Squalene; Stearic Acids; Triglycerides; Triolein

2004