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Journal of Lipid Research
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    • Research Article3

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    JLR Patient-Oriented and Epidemiological Research

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    • Patient-Oriented and Epidemiological Research
      Open Access

      Four nights of sleep restriction suppress the postprandial lipemic response and decrease satiety

      Journal of Lipid Research
      Vol. 60Issue 11p1935–1945Published online: September 4, 2019
      • Kelly M. Ness
      • Stephen M. Strayer
      • Nicole G. Nahmod
      • Margeaux M. Schade
      • Anne-Marie Chang
      • Gregory C. Shearer
      • and others
      Cited in Scopus: 9
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        Chronic sleep restriction, or inadequate sleep, is associated with increased risk of cardiometabolic disease. Laboratory studies demonstrate that sleep restriction causes impaired whole-body insulin sensitivity and glucose disposal. Evidence suggests that inadequate sleep also impairs adipose tissue insulin sensitivity and the NEFA rebound during intravenous glucose tolerance tests, yet no studies have examined the effects of sleep restriction on high-fat meal lipemia. We assessed the effect of 5 h time in bed (TIB) per night for four consecutive nights on postprandial lipemia following a standardized high-fat dinner (HFD).
        Four nights of sleep restriction suppress the postprandial lipemic response and decrease satiety
      • Patient-Oriented and Epidemiological Research
        Open Access

        Increased palmitate intake: higher acylcarnitine concentrations without impaired progression of β-oxidation

        Journal of Lipid Research
        Vol. 56Issue 9p1795–1807Published online: July 8, 2015
        • C.Lawrence Kien
        • Dwight E. Matthews
        • Matthew E. Poynter
        • Janice Y. Bunn
        • Naomi K. Fukagawa
        • Karen I. Crain
        • and others
        Cited in Scopus: 5
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          Palmitic acid (PA) is associated with higher blood concentrations of medium-chain acylcarnitines (MCACs), and we hypothesized that PA may inhibit progression of FA β-oxidation. Using a cross-over design, 17 adults were fed high PA (HPA) and low PA/high oleic acid (HOA) diets, each for 3 weeks. The [1-13C]PA and [13-13C]PA tracers were administered with food in random order with each diet, and we assessed PA oxidation (PA OX) and serum AC concentration to determine whether a higher PA intake promoted incomplete PA OX.
          Increased palmitate intake: higher acylcarnitine concentrations without impaired progression of β-oxidation1[S]
        • Patient-Oriented and Epidemiological Research
          Open Access

          Effects of n-3 FA supplementation on the release of proresolving lipid mediators by blood mononuclear cells: the OmegAD study

          Journal of Lipid Research
          Vol. 56Issue 3p674–681Published online: January 23, 2015
          • Xiuzhe Wang
          • Erik Hjorth
          • Inger Vedin
          • Maria Eriksdotter
          • Yvonne Freund-Levi
          • Lars-Olof Wahlund
          • and others
          Cited in Scopus: 59
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            Specialized proresolving mediators (SPMs) induce resolution of inflammation. SPMs are derivatives of n-3 and n-6 PUFAs and may mediate their beneficial effects. It is unknown whether supplementation with PUFAs influences the production of SPMs. Alzheimer's disease (AD) is associated with brain inflammation and reduced levels of SPMs. The OmegAD study is a randomized, double-blind, and placebo-controlled clinical trial on AD patients, in which placebo or a supplement of 1.7 g DHA and 0.6 g EPA was taken daily for 6 months.
            Effects of n-3 FA supplementation on the release of proresolving lipid mediators by blood mononuclear cells: the OmegAD study[S]
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