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    Dietary fat and physiological determinants of plasma chylomicron remnant homoeostasis in normolipidaemic subjects: insight into atherogenic risk.

    249517.docx (85.43Kb)
    Access Status
    Open access
    Authors
    Irawati, D.
    Mamo, J.
    Slivkoff-Clark, K.
    Soares, M.
    James, Tony
    Date
    2017
    Type
    Journal Article
    
    Metadata
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    Citation
    Irawati, D. and Mamo, J. and Slivkoff-Clark, K. and Soares, M. and James, T. 2017. Dietary fat and physiological determinants of plasma chylomicron remnant homoeostasis in normolipidaemic subjects: insight into atherogenic risk. British Journal of Nutrition. 117 (3): pp. 403-412.
    Source Title
    British Journal of Nutrition
    DOI
    10.1017/S0007114517000150
    ISSN
    1475-2662
    School
    School of Public Health
    Remarks

    This article has been published in a revised form in The British journal of Nutrition, http://doi.org/10.1017/S0007114517000150. This version is free to view and download for private research and study only. Not for re-distribution, re-sale or use in derivative works

    URI
    http://hdl.handle.net/20.500.11937/49885
    Collection
    • Curtin Research Publications
    Abstract

    TAG depleted remnants of postprandial chylomicrons are a risk factor for atherosclerosis. Recent studies have demonstrated that in the fasted state, the majority of chylomicrons are small enough for transcytosis to arterial subendothelial space and accelerate atherogenesis. However, the size distribution of chylomicrons in the absorptive state is unclear. This study explored in normolipidaemic subjects the postprandial distribution of the chylomicron marker, apoB-48, in a TAG-rich lipoprotein plasma fraction (Svedberg flotation rate (Sf>400), in partially hydrolysed remnants (Sf 20-400) and in a TAG-deplete fraction (Sf<20), following ingestion of isoenergetic meals with either palm oil (PO), rice bran or coconut oil. Results from this study show that the majority of fasting chylomicrons are within the potentially pro-atherogenic Sf<20 fraction (70-75 %). Following the ingestion of test meals, chylomicronaemia was also principally distributed within the Sf<20 fraction. However, approximately 40 % of subjects demonstrated exaggerated postprandial lipaemia specifically in response to the SFA-rich PO meal, with a transient shift to more buoyant chylomicron fractions. The latter demonstrates that heterogeneity in the magnitude and duration of hyper-remnantaemia is dependent on both the nature of the meal fatty acids ingested and possible metabolic determinants that influence chylomicron metabolism. The study findings reiterate that fasting plasma TAG is a poor indicator of atherogenic chylomicron remnant homoeostasis and emphasises the merits of considering specifically, chylomicron remnant abundance and kinetics in the context of atherogenic risk. Few studies address the latter, despite the majority of life being spent in the postprandial and absorptive state.

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