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      Shark liver oil supplementation enriches endogenous plasmalogens and reduces markers of dyslipidemia and inflammation

      research-article
      1 , 2 , 1 , 1 , 1 , 1 , 1 , 1 , 1 , 3 , 2 , 3 , 2 , 3 , 1 , 4 , 1 , 2 ,
      Journal of Lipid Research
      American Society for Biochemistry and Molecular Biology
      diet and dietary lipids, plasmalogens, lipidomics, lipid metabolism, inflammation, metabolic disease, immunometabolism, BH, Benjamini-Hochberg, COH, cholesterol, hsCRP, high-sensitivity C-reactive protein, LPC(O), lysoalkylphosphatidylcholine, PC, phosphatidylcholine, PC(O), alkyl phosphatidylcholine, PC(P), alkenyl phosphatidylcholine, PE(O), alkyl phosphatidylethanolamine, PE(P), alkenyl phosphatidylethanolamine, SLO, shark liver oil, TG(O), monoalkyl-diacylglycerol

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          Abstract

          Plasmalogens are membrane glycerophospholipids with diverse biological functions. Reduced plasmalogen levels have been observed in metabolic diseases; hence, increasing their levels might be beneficial in ameliorating these conditions. Shark liver oil (SLO) is a rich source of alkylglycerols that can be metabolized into plasmalogens. This study was designed to evaluate the impact of SLO supplementation on endogenous plasmalogen levels in individuals with features of metabolic disease. In this randomized, double-blind, placebo-controlled cross-over study, the participants (10 overweight or obese males) received 4-g Alkyrol® (purified SLO) or placebo (methylcellulose) per day for 3 weeks followed by a 3-week washout phase and were then crossed over to 3 weeks of the alternate placebo/Alkyrol® treatment. SLO supplementation led to significant changes in plasma and circulatory white blood cell lipidomes, notably increased levels of plasmalogens and other ether lipids. In addition, SLO supplementation significantly decreased the plasma levels of total free cholesterol, triglycerides, and C-reactive protein. These findings suggest that SLO supplementation can enrich plasma and cellular plasmalogens and this enrichment may provide protection against obesity-related dyslipidemia and inflammation.

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          Most cited references48

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          Metabolic syndrome--a new world-wide definition. A Consensus Statement from the International Diabetes Federation.

          To establish a unified working diagnostic tool for the metabolic syndrome (MetS) that is convenient to use in clinical practice and that can be used world-wide so that data from different countries can be compared. An additional aim was to highlight areas where more research into the MetS is needed. The International Diabetes Federation (IDF) convened a workshop held 12-14 May 2004 in London, UK. The 21 participants included experts in the fields of diabetes, public health, epidemiology, lipidology, genetics, metabolism, nutrition and cardiology. There were participants from each of the five continents as well as from the World Health Organization (WHO) and the National Cholesterol Education Program-Third Adult Treatment Panel (ATP III). The workshop was sponsored by an educational grant from AstraZeneca Pharmaceuticals. The consensus statement emerged following detailed discussions at the IDF workshop. After the workshop, a writing group produced a consensus statement which was reviewed and approved by all participants. The IDF has produced a new set of criteria for use both epidemiologically and in clinical practice world-wide with the aim of identifying people with the MetS to clarify the nature of the syndrome and to focus therapeutic strategies to reduce the long-term risk of cardiovascular disease. Guidance is included on how to compensate for differences in waist circumference and in regional adipose tissue distribution between different populations. The IDF has also produced recommendations for additional criteria that should be included when studying the MetS for research purposes. Finally, the IDF has identified areas where more studies are currently needed; these include research into the aetiology of the syndrome.
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            • Record: found
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            • Article: not found

            A simple method for the isolation and purification of total lipides from animal tissues.

              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              The biology of NKT cells.

              Recognized more than a decade ago, NKT cells differentiate from mainstream thymic precursors through instructive signals emanating during TCR engagement by CD1d-expressing cortical thymocytes. Their semi-invariant alphabeta TCRs recognize isoglobotrihexosylceramide, a mammalian glycosphingolipid, as well as microbial alpha-glycuronylceramides found in the cell wall of Gram-negative, lipopolysaccharide-negative bacteria. This dual recognition of self and microbial ligands underlies innate-like antimicrobial functions mediated by CD40L induction and massive Th1 and Th2 cytokine and chemokine release. Through reciprocal activation of NKT cells and dendritic cells, synthetic NKT ligands constitute promising new vaccine adjuvants. NKT cells also regulate a range of immunopathological conditions, but the mechanisms and the ligands involved remain unknown. NKT cell biology has emerged as a new field of research at the frontier between innate and adaptive immunity, providing a powerful model to study fundamental aspects of the cell and structural biology of glycolipid trafficking, processing, and recognition.
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                Author and article information

                Contributors
                Journal
                J Lipid Res
                J Lipid Res
                Journal of Lipid Research
                American Society for Biochemistry and Molecular Biology
                0022-2275
                1539-7262
                17 June 2021
                2021
                17 June 2021
                : 62
                : 100092
                Affiliations
                [1 ]Metabolomics Laboratory, Baker Heart and Diabetes Institute, Melbourne, Victoria, Australia
                [2 ]Faculty of Medicine, Nursing and Health Sciences, Monash University, Melbourne, Victoria, Australia
                [3 ]Haematopoiesis and Leukocyte Biology Laboratory, Baker Heart and Diabetes Institute, Melbourne, Victoria, Australia
                [4 ]Metabolic and Vascular Physiology Laboratory, Baker Heart and Diabetes Institute, Melbourne, Victoria, Australia
                Author notes
                []For correspondence: Peter J. Meikle peter.meikle@ 123456baker.edu.au
                Article
                S0022-2275(21)00074-2 100092
                10.1016/j.jlr.2021.100092
                8281607
                34146594
                babe26a3-6cb3-4e7b-be07-03adc3c77795
                © 2021 The Authors

                This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

                History
                : 2 April 2021
                : 27 May 2021
                Categories
                Research Article

                Biochemistry
                diet and dietary lipids,plasmalogens,lipidomics,lipid metabolism,inflammation,metabolic disease,immunometabolism,bh, benjamini-hochberg,coh, cholesterol,hscrp, high-sensitivity c-reactive protein,lpc(o), lysoalkylphosphatidylcholine,pc, phosphatidylcholine,pc(o), alkyl phosphatidylcholine,pc(p), alkenyl phosphatidylcholine,pe(o), alkyl phosphatidylethanolamine,pe(p), alkenyl phosphatidylethanolamine,slo, shark liver oil,tg(o), monoalkyl-diacylglycerol

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