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Review
. 2015:2015:520618.
doi: 10.1155/2015/520618. Epub 2015 Nov 16.

Sphingolipids in High Fat Diet and Obesity-Related Diseases

Affiliations
Review

Sphingolipids in High Fat Diet and Obesity-Related Diseases

Songhwa Choi et al. Mediators Inflamm. 2015.

Abstract

Nutrient oversupply associated with a high fat diet (HFD) significantly alters cellular metabolism, and specifically including sphingolipid metabolism. Sphingolipids are emerging as bioactive lipids that play key roles in regulating functions, in addition to their traditional roles as membrane structure. HFD enhances de novo sphingolipid synthesis and turnover of sphingolipids via the salvage pathway, resulting in the generation of ceramide, and more specifically long chain ceramide species. Additionally, HFD elevates sphingomyelin and sphingosine-1 phosphate (S1P) levels in several tissues including liver, skeletal muscle, adipose tissue, and cardiovascular tissues. HFD-stimulated sphingolipid generation contributes to systemic insulin resistance, dysregulated lipid accumulation, and cytokine expression and secretion from skeletal muscle and adipose tissues, exacerbating obesity-related conditions. Furthermore, altered sphingolipid levels, particularly ceramide and sphingomyelin, are involved in obesity-induced endothelial dysfunction and atherosclerosis. In this review, HFD-mediated sphingolipid metabolism and its impact on HFD-induced biology and pathobiology will be discussed.

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References

    1. Ogden C. L., Carroll M. D., Kit B. K., Flegal K. M. Prevalence of childhood and adult obesity in the United States, 2011-2012. The Journal of the American Medical Association. 2014;311(8):806–814. doi: 10.1001/jama.2014.732. - DOI - PMC - PubMed
    1. Hannun Y. A., Obeid L. M. Principles of bioactive lipid signalling: lessons from sphingolipids. Nature Reviews Molecular Cell Biology. 2008;9(2):139–150. doi: 10.1038/nrm2329. - DOI - PubMed
    1. Snider A. J., Orr Gandy K. A., Obeid L. M. Sphingosine kinase: role in regulation of bioactive sphingolipid mediators in inflammation. Biochimie. 2010;92(6):707–715. doi: 10.1016/j.biochi.2010.02.008. - DOI - PMC - PubMed
    1. Hornemann T., Penno A., Rütti M. F., et al. The SPTLC3 subunit of serine palmitoyltransferase generates short chain sphingoid bases. Journal of Biological Chemistry. 2009;284(39):26322–26330. doi: 10.1074/jbc.m109.023192. - DOI - PMC - PubMed
    1. Summers S. A. Ceramides in insulin resistance and lipotoxicity. Progress in Lipid Research. 2006;45(1):42–72. doi: 10.1016/j.plipres.2005.11.002. - DOI - PubMed

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