Journal
JOURNAL OF LIPID RESEARCH
Volume 52, Issue 3, Pages 509-517Publisher
ELSEVIER
DOI: 10.1194/jlr.M010595
Keywords
nervonic acid; sphingosine-1-phosphate; ceramide; sphingomyelin; cerebrosides; lipidomics
Categories
Funding
- Pennsylvania (PA) Department of Health
- Juvenile Diabetes Research Foundation
- National Eye Institute [NEI EY018336]
- American Diabetes Association [7-07-RA-80]
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Alterations in lipid metabolism may contribute to diabetic complications. Sphingolipids are essential components of cell membranes and have essential roles in homeostasis and in the initiation and progression of disease. However, the role of sphingolipids in type 1 diabetes remains largely unexplored. Therefore, we sought to quantify sphingolipid metabolites by LC-MS/MS from two animal models of type 1 diabetes (streptozotocin-induced diabetic rats and Ins2(Akita) diabetic mice) to identify putative therapeutic targets and biomarkers. The results reveal that sphingosine-1-phosphate (So1P) is elevated in both diabetic models in comparison to respective control animals. In addition, diabetic animals demonstrated reductions in plasma levels of omega-9 24:1 (nervonic acid)-containing ceramide, sphingomyelin, and cerebrosides. Reduction of 24:1-esterfied sphingolipids was also observed in liver and heart. Nutritional stress via a high-fat diet also reduced 24:1 content in the plasma and liver of mice, exacerbating the decrease in some cases where diabetes was also present. Subcutaneous insulin corrected both circulating So1P and 24:1 levels in the murine diabetic model.jlr Thus, changes in circulating sphingolipids, as evidenced by an increase in bioactive So1P and a reduction in cardio-and neuro-protective omega-9 esterified sphingolipids, may serve as biomarkers for type 1 diabetes and represent novel therapeutic targets.-Fox, T. E., M. C. Bewley, K. A. Unrath, M. M. Pedersen, R. E. Anderson, D. Y. Jung, L. S. Jefferson, J. K. Kim, S. K. Bronson, J. M. Flanagan, and M. Kester. Circulating sphingolipid biomarkers in models of type 1 diabetes. J. Lipid Res. 2011. 52: 509-517.
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